Fibonacci M747P168
Alpha
168 native Fibonacci residues on the period circle.
Clock position 168 is north. Remainder zero is displayed as 747.
Fibonacci recurrence modulo 747. The initial state (0, 1) first returns after 168 steps.
747 · 1 · 1 · 2 · 3 · 5 · 8 · 13 · 21 · 34 · 55 · 89 · 144 · 233 · 377 · 610 · 240 · 103 · 343 · 446 · 42 · 488 · 530 · 271 · 54 · 325 · 379 · 704 · 336 · 293 · 629 · 175 · 57 · 232 · 289 · 521 · 63 · 584 · 647 · 484 · 384 · 121 · 505 · 626 · 384 · 263 · 647 · 163 · 63 · 226 · 289 · 515 · 57 · 572 · 629 · 454 · 336 · 43 · 379 · 422 · 54 · 476 · 530 · 259 · 42 · 301 · 343 · 644 · 240 · 137 · 377 · 514 · 144 · 658 · 55 · 713 · 21 · 734 · 8 · 742 · 3 · 745 · 1 · 746 · 747 · 746 · 746 · 745 · 744 · 742 · 739 · 734 · 726 · 713 · 692 · 658 · 603 · 514 · 370 · 137 · 507 · 644 · 404 · 301 · 705 · 259 · 217 · 476 · 693 · 422 · 368 · 43 · 411 · 454 · 118 · 572 · 690 · 515 · 458 · 226 · 684 · 163 · 100 · 263 · 363 · 626 · 242 · 121 · 363 · 484 · 100 · 584 · 684 · 521 · 458 · 232 · 690 · 175 · 118 · 293 · 411 · 704 · 368 · 325 · 693 · 271 · 217 · 488 · 705 · 446 · 404 · 103 · 507 · 610 · 370 · 233 · 603 · 89 · 692 · 34 · 726 · 13 · 739 · 5 · 744 · 2 · 746 · 1
Beta
Interior interval sums on the native 747-position circle.
Original start: 4. No nonconstant doubling cycle in these interval sums.
Interior sums: 4, 26, 178, 1220, 892, 1289, 1408, 1097, 1042, 1715, 1252, 1073, 1030, 1655, 844, 1265, 1288, 1028, 1426, 1484, 1492, 2237, 2215, 2063, 1021, 1349, 952, 833, 1144, 1199, 526, 989, 1168, 1211, 586, 1397, 976, 953, 1213, 815, 757, 749. Modulo 747: 4, 26, 178, 473, 145, 542, 661, 350, 295, 221, 505, 326, 283, 161, 97, 518, 541, 281, 679, 737, 745, 743, 721, 569, 274, 602, 205, 86, 397, 452, 526, 242, 421, 464, 586, 650, 229, 206, 466, 68, 10, 2. First interval: clock positions 168 to 4. Endpoints excluded; wraparound included. Original phase is preserved.
4 → 26 → 178 → 473 → 145 → 542 → 661 → 350 → 295 → 221 → 505 → 326 → 283 → 161 → 97 → 518 → 541 → 281 → 679 → 737 → 745 → 743 → 721 → 569 → 274 → 602 → 205 → 86 → 397 → 452 → 526 → 242 → 421 → 464 → 586 → 650 → 229 → 206 → 466 → 68 → 10 → 2
Gamma
Primary nodal geometry.
Clockwise node order, starting from north.
Clock positions: 168, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104, 108, 112, 116, 120, 124, 128, 132, 136, 140, 144, 148, 152, 156, 160, 164. The primary selection uses native residues divisible by three, including zero. Regular triangles are drawn only when their vertices lie in this node set. Additional formations are available in Geometry summary.
747 · 3 · 21 · 144 · 240 · 42 · 54 · 336 · 57 · 63 · 384 · 384 · 63 · 57 · 336 · 54 · 42 · 240 · 144 · 21 · 3 · 747 · 744 · 726 · 603 · 507 · 705 · 693 · 411 · 690 · 684 · 363 · 363 · 684 · 690 · 411 · 693 · 705 · 507 · 603 · 726 · 744
Epsilon
M747 shares M9’s unicursal geometry. Its native values become the repeating 9–3–6 sequence when reduced to modulus 9.
Native M747 · the path is present; its native values do not meet the 3–6–9 rule.
Clock position route: 168 → 56 → 140 → 84 → 28 → 112 → 168. Python checked: exact rational circle positions and reduced traversal. Physical interpretation not assessed.
747 → 336 → 411 → 747 → 336 → 411 → 747
Fibonacci M747P168
Native sequences and detected primary geometry in one frame.
Alpha uses 168 positions; Beta uses 747. White Epsilon path: exact M9 geometry and reduced traversal; native labels retained.
Only detected primary triangles and hexagons are drawn. Shared placement is a drawing convention and does not establish biological significance.
Alpha · Beta · Gamma · Epsilon
Modulus 747 · Pisano period 168 · M9 family
This page presents the recorded explanations, sequence values and evidence status. Long coordinate tables and formation enumerations are preserved in the complete linked data. Sequence arrays longer than 240 values are abbreviated in this HTML view.
Complete record JSON · Complete record CSV · Interactive geometry
Record SHA-256: ae4356b9c9cc5a3c1875a460e9556e4c131c0779543ac7d90ea2bb65805bc6ce
Dataset: m1-m1001-v1
conventions
- index origin
- 0
- clock labels
168 · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · 11 · 12 · 13 · 14 · 15 · 16 · 17 · 18 · 19 · 20 · 21 · 22 · 23 · 24 · 25 · 26 · 27 · 28 · 29 · 30 · 31 · 32 · 33 · 34 · 35 · 36 · 37 · 38 · 39 · 40 · 41 · 42 · 43 · 44 · 45 · 46 · 47 · 48 · 49 · 50 · 51 · 52 · 53 · 54 · 55 · 56 · 57 · 58 · 59 · 60 · 61 · 62 · 63 · 64 · 65 · 66 · 67 · 68 · 69 · 70 · 71 · 72 · 73 · 74 · 75 · 76 · 77 · 78 · 79 · 80 · 81 · 82 · 83 · 84 · 85 · 86 · 87 · 88 · 89 · 90 · 91 · 92 · 93 · 94 · 95 · 96 · 97 · 98 · 99 · 100 · 101 · 102 · 103 · 104 · 105 · 106 · 107 · 108 · 109 · 110 · 111 · 112 · 113 · 114 · 115 · 116 · 117 · 118 · 119 · 120 · 121 · 122 · 123 · 124 · 125 · 126 · 127 · 128 · 129 · 130 · 131 · 132 · 133 · 134 · 135 · 136 · 137 · 138 · 139 · 140 · 141 · 142 · 143 · 144 · 145 · 146 · 147 · 148 · 149 · 150 · 151 · 152 · 153 · 154 · 155 · 156 · 157 · 158 · 159 · 160 · 161 · 162 · 163 · 164 · 165 · 166 · 167
- orientation
- clockwise from north
- zero display
- 747
- alpha circle positions
- 168
- beta circle positions
- 747
- node rule
- Native residues divisible by 3, including zero; preserves the approved M6/M9/M12 reference selection. Additional regular formations of all native values are catalogued separately.
- m1 convention
- Modulo 1 has period 1 and residue 0.
research
- focus
- OXTR gene expression
- biological significance status
- Not yet assessed
- statistical significance status
- Not yet assessed
- quantum annealing status
- Not yet performed
- tiers
- name
- Creates cellular life
- range
8 · 10
- wss score
- Not recorded
- evidence
- None recorded
- name
- Supports cellular life
- range
5 · 7
- wss score
- Not recorded
- evidence
- None recorded
- name
- Creates elemental life
- range
1 · 4
- wss score
- Not recorded
- evidence
- None recorded
- background literature
- register id
- oxtr-phase1-literature
- register version
- 2026-10-18.1
- register file
- research-register.json
- relationship
- background_context
- scope
- Shared background literature for the initial OXTR research programme across M1–M1001. Studies of related mechanisms in other systems provide context for investigation.
- publication ids
E01 · E02 · E03 · E04 · E05 · E06 · E07 · E08 · E09 · E10 · E11 · E12 · E13 · E14
- hero publication ids
E03 · E06 · E08 · E11
- modulus relevance status
- Not yet assessed
verification
- python
- Passed
- wolfram
- Passed
- scope
- Native period, sequences, regular polygon index spacing and reference Epsilon routes; no physical or biological validation.
- wolfram scope
- Native Pisano period; complete Alpha, primary Gamma indices, Beta interval sums and residues, primary equilateral-triangle and hexagon indices. Independent integer Fibonacci evaluation and SHA-256 comparisons. Extended catalogue, Chevron and native/cycle-based Epsilon are Python-checked.
- evidence
- m1001-verification.json
geometry summary
- rule version
- native-pilot-v1
- scope
- Shapes in the primary Gamma node set (native residues divisible by 3, including zero). All regular polygons on the period circle are catalogued separately with their native values; their existence alone is a property of the plotting grid.
- circle role
- Pisano-period plotting framework
- shapes
- name
- Equilateral triangle
- status
- Present
- count
- 14
- orientation
- 0° / 8.57143° / 17.1429° / 25.7143° / 34.2857° / 42.8571° / 51.4286° / 60° / 68.5714° / 77.1429° / 85.7143° / 94.2857° / 102.857° / 111.429°
- rotation degrees
- Not recorded
- rotations degrees
0 · 8.571428571428571 · 17.142857142857142 · 25.714285714285715 · 34.285714285714285 · 42.857142857142854 · 51.42857142857143 · 60 · 68.57142857142857 · 77.14285714285714 · 85.71428571428571 · 94.28571428571429 · 102.85714285714286 · 111.42857142857143
- alpha paths
0 · 56 · 112 · 0
4 · 60 · 116 · 4
8 · 64 · 120 · 8
12 · 68 · 124 · 12
16 · 72 · 128 · 16
20 · 76 · 132 · 20
24 · 80 · 136 · 24
28 · 84 · 140 · 28
32 · 88 · 144 · 32
36 · 92 · 148 · 36
40 · 96 · 152 · 40
44 · 100 · 156 · 44
48 · 104 · 160 · 48
52 · 108 · 164 · 52
- name
- Hexagon
- status
- Present
- count
- 7
- orientation
- 0° / 8.57143° / 17.1429° / 25.7143° / 34.2857° / 42.8571° / 51.4286°
- rotation degrees
- Not recorded
- rotations degrees
0 · 8.571428571428571 · 17.142857142857142 · 25.714285714285715 · 34.285714285714285 · 42.857142857142854 · 51.42857142857143
- alpha paths
0 · 28 · 56 · 84 · 112 · 140 · 0
4 · 32 · 60 · 88 · 116 · 144 · 4
8 · 36 · 64 · 92 · 120 · 148 · 8
12 · 40 · 68 · 96 · 124 · 152 · 12
16 · 44 · 72 · 100 · 128 · 156 · 16
20 · 48 · 76 · 104 · 132 · 160 · 20
24 · 52 · 80 · 108 · 136 · 164 · 24
- name
- 2D stellated octahedron
- status
- Present
- count
- 7
- orientation
- 0° / 8.57143° / 17.1429° / 25.7143° / 34.2857° / 42.8571° / 51.4286°
- rotation degrees
- Not recorded
- rotations degrees
0 · 8.571428571428571 · 17.142857142857142 · 25.714285714285715 · 34.285714285714285 · 42.857142857142854 · 51.42857142857143
- alpha paths
0 · 56 · 112 · 0
28 · 84 · 140 · 28
4 · 60 · 116 · 4
32 · 88 · 144 · 32
8 · 64 · 120 · 8
36 · 92 · 148 · 36
12 · 68 · 124 · 12
40 · 96 · 152 · 40
16 · 72 · 128 · 16
44 · 100 · 156 · 44
20 · 76 · 132 · 20
48 · 104 · 160 · 48
24 · 80 · 136 · 24
52 · 108 · 164 · 52
- name
- Chevron
- status
- Absent
- count
- 0
- orientation
- Not recorded
- rotation degrees
- Not recorded
- rotations degrees
- None recorded
- alpha paths
- None recorded
- name
- Unicursal hexagram
- status
- Absent
- count
- 0
- orientation
- Not recorded
- rotation degrees
- Not recorded
- rotations degrees
- None recorded
- alpha paths
- None recorded
- other orientations status
- Present
- epsilon rule
- A regular six-node formation must support the reference unicursal route through only 3, 6 and 9, containing all three. Rotations and reflections of the route are tested; reversed or cyclically shifted traversals are deduplicated.
alpha
- residues
0 · 1 · 1 · 2 · 3 · 5 · 8 · 13 · 21 · 34 · 55 · 89 · 144 · 233 · 377 · 610 · 240 · 103 · 343 · 446 · 42 · 488 · 530 · 271 · 54 · 325 · 379 · 704 · 336 · 293 · 629 · 175 · 57 · 232 · 289 · 521 · 63 · 584 · 647 · 484 · 384 · 121 · 505 · 626 · 384 · 263 · 647 · 163 · 63 · 226 · 289 · 515 · 57 · 572 · 629 · 454 · 336 · 43 · 379 · 422 · 54 · 476 · 530 · 259 · 42 · 301 · 343 · 644 · 240 · 137 · 377 · 514 · 144 · 658 · 55 · 713 · 21 · 734 · 8 · 742 · 3 · 745 · 1 · 746 · 0 · 746 · 746 · 745 · 744 · 742 · 739 · 734 · 726 · 713 · 692 · 658 · 603 · 514 · 370 · 137 · 507 · 644 · 404 · 301 · 705 · 259 · 217 · 476 · 693 · 422 · 368 · 43 · 411 · 454 · 118 · 572 · 690 · 515 · 458 · 226 · 684 · 163 · 100 · 263 · 363 · 626 · 242 · 121 · 363 · 484 · 100 · 584 · 684 · 521 · 458 · 232 · 690 · 175 · 118 · 293 · 411 · 704 · 368 · 325 · 693 · 271 · 217 · 488 · 705 · 446 · 404 · 103 · 507 · 610 · 370 · 233 · 603 · 89 · 692 · 34 · 726 · 13 · 739 · 5 · 744 · 2 · 746 · 1
- display values
747 · 1 · 1 · 2 · 3 · 5 · 8 · 13 · 21 · 34 · 55 · 89 · 144 · 233 · 377 · 610 · 240 · 103 · 343 · 446 · 42 · 488 · 530 · 271 · 54 · 325 · 379 · 704 · 336 · 293 · 629 · 175 · 57 · 232 · 289 · 521 · 63 · 584 · 647 · 484 · 384 · 121 · 505 · 626 · 384 · 263 · 647 · 163 · 63 · 226 · 289 · 515 · 57 · 572 · 629 · 454 · 336 · 43 · 379 · 422 · 54 · 476 · 530 · 259 · 42 · 301 · 343 · 644 · 240 · 137 · 377 · 514 · 144 · 658 · 55 · 713 · 21 · 734 · 8 · 742 · 3 · 745 · 1 · 746 · 747 · 746 · 746 · 745 · 744 · 742 · 739 · 734 · 726 · 713 · 692 · 658 · 603 · 514 · 370 · 137 · 507 · 644 · 404 · 301 · 705 · 259 · 217 · 476 · 693 · 422 · 368 · 43 · 411 · 454 · 118 · 572 · 690 · 515 · 458 · 226 · 684 · 163 · 100 · 263 · 363 · 626 · 242 · 121 · 363 · 484 · 100 · 584 · 684 · 521 · 458 · 232 · 690 · 175 · 118 · 293 · 411 · 704 · 368 · 325 · 693 · 271 · 217 · 488 · 705 · 446 · 404 · 103 · 507 · 610 · 370 · 233 · 603 · 89 · 692 · 34 · 726 · 13 · 739 · 5 · 744 · 2 · 746 · 1
beta
- interval sums
4 · 26 · 178 · 1220 · 892 · 1289 · 1408 · 1097 · 1042 · 1715 · 1252 · 1073 · 1030 · 1655 · 844 · 1265 · 1288 · 1028 · 1426 · 1484 · 1492 · 2237 · 2215 · 2063 · 1021 · 1349 · 952 · 833 · 1144 · 1199 · 526 · 989 · 1168 · 1211 · 586 · 1397 · 976 · 953 · 1213 · 815 · 757 · 749
- interval residues
4 · 26 · 178 · 473 · 145 · 542 · 661 · 350 · 295 · 221 · 505 · 326 · 283 · 161 · 97 · 518 · 541 · 281 · 679 · 737 · 745 · 743 · 721 · 569 · 274 · 602 · 205 · 86 · 397 · 452 · 526 · 242 · 421 · 464 · 586 · 650 · 229 · 206 · 466 · 68 · 10 · 2
- display cycle
4 · 26 · 178 · 473 · 145 · 542 · 661 · 350 · 295 · 221 · 505 · 326 · 283 · 161 · 97 · 518 · 541 · 281 · 679 · 737 · 745 · 743 · 721 · 569 · 274 · 602 · 205 · 86 · 397 · 452 · 526 · 242 · 421 · 464 · 586 · 650 · 229 · 206 · 466 · 68 · 10 · 2
- minimal cycle
4 · 26 · 178 · 473 · 145 · 542 · 661 · 350 · 295 · 221 · 505 · 326 · 283 · 161 · 97 · 518 · 541 · 281 · 679 · 737 · 745 · 743 · 721 · 569 · 274 · 602 · 205 · 86 · 397 · 452 · 526 · 242 · 421 · 464 · 586 · 650 · 229 · 206 · 466 · 68 · 10 · 2
- native doubling
- false
- recognised doubling cycle
- Not recorded
- rotation to recognised
- Not recorded
- m9 doubling cycle present
- false
- start value
- 4
- start interval clock positions
168 · 4
- start interval values
1 · 1 · 2
- circle positions
- 747
- cycle length
- 42
- endpoint rule
- Exclude endpoints, include wraparound; raw residues used for sums. Empty interiors sum to zero.
gamma
- alpha indices
0 · 4 · 8 · 12 · 16 · 20 · 24 · 28 · 32 · 36 · 40 · 44 · 48 · 52 · 56 · 60 · 64 · 68 · 72 · 76 · 80 · 84 · 88 · 92 · 96 · 100 · 104 · 108 · 112 · 116 · 120 · 124 · 128 · 132 · 136 · 140 · 144 · 148 · 152 · 156 · 160 · 164
- clock positions
168 · 4 · 8 · 12 · 16 · 20 · 24 · 28 · 32 · 36 · 40 · 44 · 48 · 52 · 56 · 60 · 64 · 68 · 72 · 76 · 80 · 84 · 88 · 92 · 96 · 100 · 104 · 108 · 112 · 116 · 120 · 124 · 128 · 132 · 136 · 140 · 144 · 148 · 152 · 156 · 160 · 164
- clockwise values
747 · 3 · 21 · 144 · 240 · 42 · 54 · 336 · 57 · 63 · 384 · 384 · 63 · 57 · 336 · 54 · 42 · 240 · 144 · 21 · 3 · 747 · 744 · 726 · 603 · 507 · 705 · 693 · 411 · 690 · 684 · 363 · 363 · 684 · 690 · 411 · 693 · 705 · 507 · 603 · 726 · 744
- triangle paths
0 · 56 · 112 · 0
4 · 60 · 116 · 4
8 · 64 · 120 · 8
12 · 68 · 124 · 12
16 · 72 · 128 · 16
20 · 76 · 132 · 20
24 · 80 · 136 · 24
28 · 84 · 140 · 28
32 · 88 · 144 · 32
36 · 92 · 148 · 36
40 · 96 · 152 · 40
44 · 100 · 156 · 44
48 · 104 · 160 · 48
52 · 108 · 164 · 52
epsilon status
Null: no tested regular six-node reference traversal contains only 3, 6 and 9 with all three present.epsilon assessment
- rule version
- native-epsilon-diagnostics-v1
- native 369 present
- false
- candidate count
- 28
- absence reason
- No tested six-node formation contains only 3, 6 and 9 with all three present.
- reference path available
- true
reduction to m9
- version
- m9-reduction-v1
- target modulus
- 9
- status
- Exact match
- applicable
- true
- research question
- Does the shared M9 pattern have shared biological relevance, or does native-modulus complexity change it? Unassessed: requires peer-reviewed evidence, in silico modelling (including proposed CUDA/CUDA-Q work), and appropriate experimental validation. No spatial-dimension claim or WSS score follows from this arithmetic match.
- biological significance
- Not yet assessed
- native data preserved
- true
- repeat count
- 7
- checks
- alpha
- true
- gamma
- true
- beta
- true
- gamma indices
- true
- alpha residues
0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 0 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 0 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1
- alpha display
9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1 · 9 · 1 · 1 · 2 · 3 · 5 · 8 · 4 · 3 · 7 · 1 · 8 · 9 · 8 · 8 · 7 · 6 · 4 · 1 · 5 · 6 · 2 · 8 · 1
- gamma residues
0 · 3 · 3 · 0 · 6 · 6 · 0 · 3 · 3 · 0 · 6 · 6 · 0 · 3 · 3 · 0 · 6 · 6 · 0 · 3 · 3 · 0 · 6 · 6 · 0 · 3 · 3 · 0 · 6 · 6 · 0 · 3 · 3 · 0 · 6 · 6 · 0 · 3 · 3 · 0 · 6 · 6
- gamma display
9 · 3 · 3 · 9 · 6 · 6 · 9 · 3 · 3 · 9 · 6 · 6 · 9 · 3 · 3 · 9 · 6 · 6 · 9 · 3 · 3 · 9 · 6 · 6 · 9 · 3 · 3 · 9 · 6 · 6 · 9 · 3 · 3 · 9 · 6 · 6 · 9 · 3 · 3 · 9 · 6 · 6
- beta residues
4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2
- beta display
4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2 · 4 · 8 · 7 · 5 · 1 · 2
- recognised beta cycle
1 · 2 · 4 · 8 · 7 · 5
- phase preserved
- true
- projected chevron
- true
- projected beta circle positions
- 9
- gamma same single circle positions
- false
- geometry note
- M18 and M9 share the same 24-position Gamma geometry. Reduced Beta is plotted on a nine-position circle. Longer periods require folding into 24-position cycles; their full circles are not identical.
- identity
- (F_n mod (9k)) mod 9 = F_n mod 9
- interpretation
- Exact reduction is a mathematical consequence of divisibility, not independent evidence of statistical or biological significance. Native Epsilon remains unchanged.
- verification
- Python full-period comparison
research register
- schema version
- 1.0.0
- id
- oxtr-phase1-literature
- version
- 2026-10-18.1
- title
- First Principles Genomics — research register
- initial biological focus
- OXTR
- scope
- Shared background literature for the initial OXTR research programme across M1–M1001. Studies of related mechanisms in other systems provide context for investigation.
- relationship to atlas
- background_context
- modulus relevance status
- Not yet assessed
- hypothesis reference record id
- fibonacci-m9-p24
- hypothesis
- The Alpha, Beta, Gamma and Epsilon sequences of M9P24 may offer useful descriptions of biological timing, cellular division and molecular organisation in the context of OXTR. Bioinformatics and in silico modelling provide the planned means of investigation.
- interpretation
- Publication findings describe their original experimental systems. Links from Atlas records identify shared reading; a sequence-to-biology correspondence remains open for assessment.
- publication count
- 14
- hero publication ids
E03 · E06 · E08 · E11
- hero selection
- Four lead references within the fourteen unique publications, one for each theme.
- wss
- status
- Awaiting assessment
- score
- Not recorded
- meaning
- Future assessment of relevance to individual Atlas records. Publication trust scores remain separate from WSS.
- appraisal method
- id
- provisional-editorial-v1
- label
- Provisional editorial trust
- range
0 · 10
- purpose
- Prioritise closer reading of reported findings. This is an editorial assessment, without calibration or independent peer review.
- components
- design
- range
0 · 3
- criteria
- 0
- Insufficient information
- 1
- Descriptive observation
- 2
- Structured measurement or comparative design
- 3
- Controlled mechanistic test or quantitative prediction tested by manipulation
- validation
- range
0 · 3
- criteria
- 0
- Unassessed
- 1
- Limited or abstract-level corroboration
- 2
- Complementary evidence within the paper
- 3
- Independent replication appraised
- review
- range
0 · 3
- criteria
- 0
- Unreviewed
- 1
- Abstract, metadata or figure descriptions
- 2
- Selected full-text sections
- 3
- Main text, relevant methods/results and captions reviewed
- provenance
- range
0 · 1
- criteria
- 0
- Unverified
- 1
- Verified primary peer-reviewed publication
- independent replication appraisal
- Not yet completed for this collection
- citation policy
- Crossref cited-by counts are a dated contextual snapshot and contribute no points. Coverage depends on deposited references. Unavailable counts remain null.
- journal policy
- Journal reputation and impact factor contribute no points.
- jadad policy
- Jadad concerns reporting of randomised clinical trials. It is not applicable to these fourteen study designs; no numeric Jadad score is assigned.
- publications
- id
- E01
- title
- Reconstitution of circadian oscillation of cyanobacterial KaiC phosphorylation in vitro
- author
- Nakajima et al.
- year
- 2005
- journal
- Science
- doi
- 10.1126/science.1108451
- theme
- Alpha · circadian timing
- hero
- Not recorded
- methods
- Purified cyanobacterial clock proteins; biochemical reconstitution
- finding
- KaiA, KaiB, KaiC and ATP supported self-sustaining phosphorylation oscillation. Temperature compensation and agreement between mutant periods in vitro and in vivo strengthened the biological interpretation.
- relevance
- direct evidence for a molecular timing mechanism; a broad Alpha reference independent of OXTR.
- limit
- biochemical reconstruction is more informative about mechanism than visual analogy. It is a cyanobacterial system, not a mammalian receptor study, and does not support a universal exact 24-hour period or M9 correspondence.
- access
- primary abstract and publication metadata. Replication and detailed methods require full-text appraisal before a formal quality rating.
- score Parts
- design
- 3
- validation
- 1
- review
- 1
- provenance
- 1
- score
- 6
- score Reason
- Molecular reconstitution tests a timing mechanism; appraisal currently covers the abstract and metadata.
- jadad
- Not applicable
- citation Count
- 1020
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Reconstitution of Circadian Oscillation of Cyanobacterial KaiC Phosphorylation in Vitro
- id
- E02
- title
- Phase locking and multiple oscillating attractors for the coupled mammalian clock and cell cycle
- author
- Feillet et al.
- year
- 2014
- journal
- PNAS
- doi
- 10.1073/pnas.1320474111
- theme
- Alpha / Beta · cycle coupling
- hero
- Not recorded
- methods
- Mouse fibroblasts; live-cell imaging and modelling
- finding
- live imaging of proliferating mouse fibroblasts, combined with modelling, identified phase locking and additional clock states under different conditions.
- relevance
- direct support for studying relationships between biological cycles; connects the Alpha and Beta research themes without making them equivalent.
- limit
- single-cell observations support the dynamical interpretation. Culture conditions and synchronisation matter, and related cells are not automatically independent replicates. No modular doubling or Atlas geometry was tested.
- access
- primary abstract and selected results, including period distributions. A phase-space representation is not evidence of a physical toroidal cell structure.
- score Parts
- design
- 2
- validation
- 2
- review
- 2
- provenance
- 1
- score
- 7
- score Reason
- Live-cell observations and modelling provide complementary evidence for phase locking; selected results appraised.
- jadad
- Not applicable
- citation Count
- 216
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Phase locking and multiple oscillating attractors for the coupled mammalian clock and cell cycle
- id
- E03
- title
- Interaction between time-of-day and oxytocin efficacy in mice and humans with and without gestational diabetes
- author
- Duong et al.
- year
- 2026 (online 2025)
- journal
- Molecular Metabolism
- doi
- 10.1016/j.molmet.2025.102269
- theme
- Alpha · circadian regulation
- hero
- alpha
- methods
- Mouse genetics; human cells; retrospective human records
- finding
- mouse experiments support BMAL1 regulation of Oxtr and time-dependent oxytocin responsiveness. Human myometrial-cell experiments and records from 2,367 patients add distinct translational observations.
- relevance
- a direct OXTR connection to the Alpha theme.
- limit
- genetic perturbation and promoter experiments strengthen mechanism. Animal, cell and retrospective components need separate appraisal; the human observations can be confounded. Uterine findings do not establish effects in brain tissue.
- access
- final publication abstract and selected full-text results. The 2024 preprint is superseded for this register and is not counted as another study.
- score Parts
- design
- 3
- validation
- 2
- review
- 2
- provenance
- 1
- score
- 8
- score Reason
- Genetic and promoter experiments support mechanism; the human observational component has separate confounding limits.
- jadad
- Not applicable
- citation Count
- 3
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Interaction between time-of-day and oxytocin efficacy in mice and humans with and without gestational diabetes
- id
- E04
- title
- Cryptochromes mediate rhythmic repression of the glucocorticoid receptor
- author
- Lamia et al.
- year
- 2011
- journal
- Nature
- doi
- 10.1038/nature10700
- theme
- Alpha · receptor regulation
- hero
- Not recorded
- methods
- Mouse cells and mice; genetic and biochemical experiments
- finding
- Cry1/Cry2 interacted with the glucocorticoid receptor and altered glucocorticoid-responsive transcription in mouse cells, with related metabolic phenotypes in mice.
- relevance
- direct circadian–receptor evidence provides a natural NR3C1 example beyond oxytocin.
- limit
- molecular interactions, genetic perturbations and physiological observations complement one another. Multiple pathways change in knockout animals; the results do not isolate a universal geometric explanation or establish human clinical effects.
- access
- primary abstract and selected experimental/results text. NR3C1 identifies the receptor target; the principal genetic perturbations here involved cryptochromes.
- score Parts
- design
- 3
- validation
- 2
- review
- 2
- provenance
- 1
- score
- 8
- score Reason
- Genetic perturbations, molecular interactions and physiological measurements support the reported mechanism.
- jadad
- Not applicable
- citation Count
- 550
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Cryptochromes mediate rhythmic repression of the glucocorticoid receptor
- id
- E05
- title
- Experimental and theoretical study of mitotic spindle orientation
- author
- Théry et al.
- year
- 2007
- journal
- Nature
- doi
- 10.1038/nature05786
- theme
- Beta · mitotic geometry
- hero
- Not recorded
- methods
- Human HeLa cells; controlled adhesion geometry and modelling
- finding
- controlled adhesion patterns in human HeLa cells, combined with a physical model, accounted for spindle-orientation distributions across different microenvironment geometries.
- relevance
- direct evidence that geometry is a meaningful biological variable; supports interest in the Beta/division theme and related shape families.
- limit
- manipulation of the cell environment offers more than an observational resemblance. The model uses specific force assumptions and a transformed cell line. Division orientation is distinct from division rate, population doubling or a Fibonacci sequence.
- access
- publisher abstract and figure descriptions. Full methods and sample accounting remain to be appraised.
- score Parts
- design
- 3
- validation
- 1
- review
- 1
- provenance
- 1
- score
- 6
- score Reason
- Controlled adhesion geometry tests a quantitative model; full methods and sample accounting remain open for appraisal.
- jadad
- Not applicable
- citation Count
- 424
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Experimental and theoretical study of mitotic spindle orientation
- id
- E06
- title
- Oxytocin promotes epicardial cell activation and heart regeneration after cardiac injury
- author
- Wasserman et al.
- year
- 2022
- journal
- Frontiers in Cell and Developmental Biology
- doi
- 10.3389/fcell.2022.985298
- theme
- Beta · proliferation
- hero
- beta
- methods
- Human stem-cell-derived epicardial cells and zebrafish
- finding
- OXT promoted activation and proliferation-related outcomes in human stem-cell-derived epicardial cells; OXTR knockdown removed the response. Zebrafish experiments supplied a separate regeneration context.
- relevance
- a direct OXTR-related example for the Beta research theme.
- limit
- receptor knockdown strengthens causal interpretation within the model. Check independent cell lines and differentiation batches; images are subsamples, not donors. Cultured epicardial cells and fish regeneration do not establish regeneration of adult human hearts.
- access
- primary full-text methods/results and relevant figure captions, including OXTR knockdown and proliferation measurements.
- score Parts
- design
- 3
- validation
- 2
- review
- 3
- provenance
- 1
- score
- 9
- score Reason
- Receptor knockdown provides a mechanistic test alongside cell and zebrafish experiments; methods and results appraised.
- jadad
- Not applicable
- citation Count
- 25
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Oxytocin promotes epicardial cell activation and heart regeneration after cardiac injury
- id
- E07
- title
- Oxytocin stimulates hippocampal neurogenesis via oxytocin receptor expressed in CA3 pyramidal neurons
- author
- Lin et al.
- year
- 2017
- journal
- Nature Communications
- doi
- 10.1038/s41467-017-00675-5
- theme
- Beta · survival / proliferation
- hero
- Not recorded
- methods
- Mice; conditional Oxtr deletion
- finding
- conditional Oxtr deletion in mouse hippocampal excitatory neurons affected survival and maturation of newly generated neurons, while measured progenitor proliferation and early differentiation were unchanged.
- relevance
- direct evidence that the biological outcome must be named precisely. It bounds generalisations from E06 without contradicting a different tissue-specific finding.
- limit
- conditional genetics help localise the process. Appraise cell-type specificity, blinding and precision; an unchanged measured outcome does not prove absence of every possible effect.
- access
- primary results/discussion. Retained deliberately to avoid presenting all OXTR growth-related findings as evidence of duplication.
- score Parts
- design
- 3
- validation
- 2
- review
- 2
- provenance
- 1
- score
- 8
- score Reason
- Conditional genetics and cell-outcome measurements distinguish survival from proliferation in this mouse system.
- jadad
- Not applicable
- citation Count
- 149
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Oxytocin stimulates hippocampal neurogenesis via oxytocin receptor expressed in CA3 pyramidal neurons
- id
- E08
- title
- Structural basis for the activation and ligand recognition of the human oxytocin receptor
- author
- Waltenspühl et al.
- year
- 2022
- journal
- Nature Communications
- doi
- 10.1038/s41467-022-31325-0
- theme
- Gamma · molecular recognition
- hero
- gamma
- methods
- Engineered human receptor complex; cryo-EM and functional assays
- finding
- cryo-EM at 3.2 Å and functional experiments characterised OXT recognition and receptor activation. All nine peptide residues participate in binding.
- relevance
- a direct structural foundation for Gamma's molecular-recognition theme; useful context, but not confirmation, for the OXT-specific Epsilon proposal.
- limit
- structure–function comparisons strengthen interpretation. Receptor stabilisation and an engineered G protein affect generalisation. The six-residue disulfide loop is not itself an aromatic hexagon; the reported contacts do not establish an Epsilon trajectory.
- access
- full primary article main text, receptor-engineering description and functional-assay captions. No new molecular analysis performed.
- score Parts
- design
- 3
- validation
- 2
- review
- 3
- provenance
- 1
- score
- 9
- score Reason
- Structural observations and functional residue tests provide complementary evidence; main text and assay descriptions appraised.
- jadad
- Not applicable
- citation Count
- 46
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Structural basis for the activation and ligand recognition of the human oxytocin receptor
- id
- E09
- title
- X-ray structures and mechanism of the human serotonin transporter
- author
- Coleman, Green & Gouaux
- year
- 2016
- journal
- Nature
- doi
- 10.1038/nature17629
- theme
- Gamma · molecular recognition
- hero
- Not recorded
- methods
- Engineered human serotonin transporter; crystallography and assays
- finding
- structures of human SERT bound to antidepressants identified central and allosteric binding sites and explained aspects of inhibitor recognition.
- relevance
- direct structural evidence broadens Gamma beyond OXTR to SLC6A4.
- limit
- structural and binding/transport measurements are complementary. Thermostabilised constructs were used; the ts3 construct had no detectable transport activity. Results describe particular inhibitor-bound conformations rather than every physiological state.
- access
- publisher abstract and selected primary methods/results. These data concern the protein product and ligand recognition, not regulation of SLC6A4 gene expression.
- score Parts
- design
- 2
- validation
- 2
- review
- 2
- provenance
- 1
- score
- 7
- score Reason
- Structures and functional measurements complement one another; engineered constructs constrain interpretation.
- jadad
- Not applicable
- citation Count
- 674
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- X-ray structures and mechanism of the human serotonin transporter
- id
- E10
- title
- Structure of a D2 dopamine receptor–G-protein complex in a lipid membrane
- author
- Yin et al.
- year
- 2020
- journal
- Nature
- doi
- 10.1038/s41586-020-2379-5
- theme
- Gamma · molecular recognition
- hero
- Not recorded
- methods
- Engineered human DRD2 complex in a lipid membrane; cryo-EM
- finding
- cryo-EM characterised an agonist-bound DRD2–Gi complex within a reconstituted phospholipid membrane, identifying receptor, G-protein and lipid interactions.
- relevance
- direct evidence for the structural context of molecular recognition; another Gamma hero example.
- limit
- including a lipid environment improves contextual relevance relative to isolated detergent structures. The receptor complex is engineered and ligand-bound; it does not represent every receptor state or establish clinical outcomes.
- access
- primary abstract and selected full-text structural results, with deposited structural metadata checked. No geometric correspondence to the Atlas was analysed.
- score Parts
- design
- 2
- validation
- 1
- review
- 2
- provenance
- 1
- score
- 6
- score Reason
- A membrane-reconstituted structural observation provides a defined molecular state; independent functional validation needs fuller appraisal.
- jadad
- Not applicable
- citation Count
- 199
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Structure of a D2 dopamine receptor–G-protein complex in a lipid membrane
- id
- E11
- title
- Assembly of a π–π stack of ligands in the binding site of an acetylcholine-binding protein
- author
- Stornaiuolo et al.
- year
- 2013
- journal
- Nature Communications
- doi
- 10.1038/ncomms2900
- theme
- Epsilon · aromatic stacking
- hero
- epsilon
- methods
- Molluscan binding protein; crystallography and solution assays
- finding
- an Aplysia acetylcholine-binding protein accommodated a stack of three aromatic ligands. Solution binding measurements supported the structural observation.
- relevance
- direct experimental support for π-stacking as a molecular-recognition phenomenon; an Epsilon reference that does not depend on OXTR.
- limit
- crystallography, mutagenesis and solution assays help address crystallographic-artifact concerns. This soluble molluscan protein is a model for receptor ligand-binding domains, not a complete human receptor. Neither the three-ligand count nor the stacked geometry establishes the Atlas traversal.
- access
- full primary main text, including solution validation and scope of the receptor model.
- score Parts
- design
- 3
- validation
- 2
- review
- 3
- provenance
- 1
- score
- 9
- score Reason
- Structures, mutagenesis and solution assays support the binding interpretation; full main text appraised.
- jadad
- Not applicable
- citation Count
- 66
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Assembly of a π–π stack of ligands in the binding site of an acetylcholine-binding protein
- id
- E12
- title
- Targeted disruption of pi–pi stacking in Malaysian banana lectin reduces mitogenicity while preserving antiviral activity
- author
- Covés-Datson et al.
- year
- 2021
- journal
- Scientific Reports
- doi
- 10.1038/s41598-020-80577-7
- theme
- Epsilon · aromatic stacking
- hero
- Not recorded
- methods
- Engineered plant lectin; structures and cellular assays
- finding
- an F84T mutation disrupted aromatic stacking in Malay BanLec, reduced mitogenic activity and retained antiviral activity in the studied assays.
- relevance
- a direct structure–function example for Epsilon; also connects molecular interactions with proliferation as a biological outcome.
- limit
- structural checks and functional comparisons strengthen the rationale. Mutation can change several properties simultaneously, so this is not a pure isolation of one energetic contribution. Plant-lectin effects do not establish OXTR behaviour or clinical benefit.
- access
- primary abstract and main structural/results sections. Published in 2021 despite “2020” appearing within the DOI.
- score Parts
- design
- 3
- validation
- 2
- review
- 2
- provenance
- 1
- score
- 8
- score Reason
- Targeted mutation and structural / cellular comparisons connect aromatic organisation with biological outcomes.
- jadad
- Not applicable
- citation Count
- 24
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Targeted disruption of pi–pi stacking in Malaysian banana lectin reduces mitogenicity while preserving antiviral activity
- id
- E13
- title
- Reconstruction of molecular orbital densities from photoemission data
- author
- Puschnig et al.
- year
- 2009
- journal
- Science
- doi
- 10.1126/science.1176105
- theme
- Valence electron orbitals
- hero
- Not recorded
- methods
- Organic molecular films; photoemission and calculations
- finding
- photoemission measurements and Fourier reconstruction yielded orbital-density distributions for pentacene films and p-sexiphenyl monolayers, compared with density-functional calculations.
- relevance
- direct physics evidence for studying spatial electronic structure; contextual to the valence-electron theme and more distant from biological significance.
- limit
- comparison of measurement and theory is valuable. Reconstruction is model-dependent and the samples are non-living materials. Orbital densities are not classical electron orbits or evidence of unicursal electron motion.
- access
- primary abstract and metadata. No biological role, creation-of-life claim or numeric WSS assignment follows from this paper.
- score Parts
- design
- 2
- validation
- 1
- review
- 1
- provenance
- 1
- score
- 5
- score Reason
- Measurement and reconstruction are compared with calculations; current appraisal is abstract-level.
- jadad
- Not applicable
- citation Count
- 334
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- Reconstruction of Molecular Orbital Densities from Photoemission Data
- id
- E14
- title
- CD38 is critical for social behaviour by regulating oxytocin secretion
- author
- Jin et al.
- year
- 2007
- journal
- Nature
- doi
- 10.1038/nature05526
- theme
- Supporting OXT context
- hero
- Not recorded
- methods
- Mice; Cd38 knockout and rescue experiments
- finding
- Cd38-knockout mice showed altered oxytocin secretion and behavioural phenotypes. Oxytocin replacement or hypothalamic delivery of human CD38 rescued selected outcomes.
- relevance
- direct support for CD38 involvement in the oxytocin system. Retained as supporting hero context without forcing it into a particular sequence family.
- limit
- knockout plus rescue strengthens causal interpretation in mice. Global deletion, behavioural measurement and human translation require careful appraisal. This concerns secretion, not proof of OXTR-expression regulation or geometric correspondence.
- access
- primary abstract and figure descriptions. Full methods are needed before formal risk-of-bias grading.
- score Parts
- design
- 3
- validation
- 1
- review
- 1
- provenance
- 1
- score
- 6
- score Reason
- Knockout and rescue experiments test the secretion mechanism; full methods remain open for appraisal.
- jadad
- Not applicable
- citation Count
- 585
- citation Source
- Crossref cited-by count
- citation Checked
- 17 October 2026
- crossref Title
- CD38 is critical for social behaviour by regulating oxytocin secretion
formation interval encoding
- version
- alpha-endpoints-v1
- rule
- For each formation interval, walk clockwise from from_index + 1 to to_index, excluding both endpoints and wrapping modulo P. Read values from alpha.residues. Endpoints, sum and residue are retained.