CoChat
Sign Up
Cited by 110Muscle Physiology and DisordersGenetics and Neurodevelopmental DisordersNeurogenetic and Muscular Disorders Research

The DOI matches its Crossref record.

Dystrophin in the Nervous System

Open access
Lidov, Hart G.W.·1996·Brain Pathology
DOI 10.1111/j.1750-3639.1996.tb00783.x
Open this paper in CoChat — free accountOpen PDF

Abstract

The most important finding from psychometric studies is that the cognitive capacity is distributed a priori (relative to the molecular genetic data--for Department of Pathology, Children's Hospital, 300 Longwood Ave.. Boston, MA 021 15 unimodaly in the Duchenne population.This argues Duchenne Muscular Dystrophy and Cognitive Function

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/j.1750-3639.1996.tb00783.x

Cites

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

No references could be resolved yet.

Research works printed but not linked: 110

  1. AhnAH FeenerCA GussoniE. YoshidaM. OzawaE. KunkelLM(1996)The three human syntrophin genes are expressed in diverse tissues have distinct chromosomal locations and each bind to dystrophin and its relatives.J Biol Chem(in press). · DOI
  2. 10.1073/pnas.91.10.4446 · DOI
  3. 10.1111/j.1469-8749.1991.tb14797.x · DOI
  4. 10.1016/0166-2236(90)90001-Q · DOI
  5. 10.1042/bj2720557 · DOI
  6. 10.1002/mus.880060702 · DOI
  7. 10.1038/ng1195-266 · DOI
  8. 10.1016/0896-6273(94)90324-7 · DOI
  9. 10.1073/pnas.88.4.1276 · DOI
  10. 10.1016/0960-8966(94)90072-8 · DOI
  11. 10.1007/BF01799614 · DOI
  12. 10.1111/j.1469-8749.1995.tb12000.x · DOI
  13. 10.1007/BF00858726 · DOI
  14. 10.1038/ng0593-77 · DOI
  15. 10.1016/0896-6273(94)90463-4 · DOI
  16. 10.1038/344064a0 · DOI
  17. 10.1038/333858a0 · DOI
  18. Cibis GW, 1993, The effects of dystrophin gene mutations on the ERG in mice and humans, Inves Ophthal Vis Sci, 34, 3646
  19. 10.1111/j.1471-4159.1993.tb03169.x · DOI
  20. 10.1111/j.1469-8749.1968.tb02974.x · DOI
  21. 10.1093/brain/117.1.1-a · DOI
  22. 10.1038/ng0593-87 · DOI
  23. 10.1093/hmg/4.5.837 · DOI
  24. 10.1016/0166-4328(94)00144-5 · DOI
  25. 10.1016/0960-8966(91)90118-C · DOI
  26. Dunnen JT, 1989, Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications, Am J Hum Genet, 45, 835
  27. 10.1093/brain/92.4.805 · DOI
  28. Duchenne GB, 1861, De l'e/ectrisation localisee et de son application a'la pathologere et a'la therapeutique
  29. Emery A., 1988, Duchenne Muscular Dystrophy, 1
  30. 10.1523/JNEUROSCI.05-12-03270.1985 · DOI · Paper page
  31. 10.1016/0092-8674(91)90035-W · DOI
  32. 10.1172/JCI117250 · DOI
  33. Gee SH, 1993, Laminin‐binding protein 120 from brain is closely related to the dystrophinassociated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin, J Bio Chem, 268, 14972, 10.1016/S0021-9258(18)82427-9 · DOI
  34. 10.1016/0092-8674(94)90052-3 · DOI
  35. 10.1016/0166-2236(91)90105-4 · DOI
  36. 10.1097/00001756-199112000-00011 · DOI
  37. 10.1097/00001756-199504190-00017 · DOI
  38. 10.1093/hmg/3.9.1589 · DOI
  39. 10.1093/hmg/1.7.505 · DOI
  40. 10.1083/jcb.119.4.811 · DOI
  41. 10.1016/0304-3940(92)90890-J · DOI
  42. 10.1016/0304-3940(92)90309-U · DOI
  43. 10.1038/355696a0 · DOI
  44. 10.1016/0887-8994(88)90047-1 · DOI
  45. 10.1016/0304-3940(91)90828-H · DOI
  46. 10.1002/ana.410320418 · DOI
  47. Karagan NJ, 1981, Intellectual functioning in non‐Duchenne muscular dystrophy, Neurology, 31, 448, 10.1212/WNL.31.4_Part_2.448 · DOI
  48. 10.1016/0960-8966(91)90023-L · DOI
  49. 10.1083/jcb.119.2.357 · DOI
  50. 10.1002/ana.410380315 · DOI
  51. 10.1073/pnas.89.23.11642 · DOI
  52. Korenberg JR, 1990, Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype, Am J Hum Genet, 47, 236
  53. 10.1002/jcb.240270411 · DOI
  54. 10.1002/cne.902800204 · DOI
  55. 10.1073/pnas.89.12.5346 · DOI
  56. 10.1038/348725a0 · DOI
  57. 10.1016/0306-4522(93)90392-S · DOI
  58. 10.1093/hmg/4.3.329 · DOI
  59. 10.1007/BF01939382 · DOI
  60. 10.1002/jnr.490400208 · DOI
  61. Lim LE, 1995, β‐sarcoglycan: characterization and role in limbgirdle muscular dystrophy linked to 4q12, Nature Genetics, 11, 257, 10.1038/ng1195-257 · DOI
  62. Lindlof M., 1989, Gene deletions in X‐linked muscular dystrophy, Am J Hum Genet, 44, 496
  63. 10.1002/ana.410380305 · DOI
  64. 10.1016/0960-8966(91)90041-P · DOI
  65. 10.1136/adc.49.2.118 · DOI
  66. 10.1016/0014-5793(93)80695-Q · DOI
  67. 10.1073/pnas.91.21.9690 · DOI
  68. 10.1073/pnas.89.6.2461 · DOI
  69. 10.1126/science.7939688 · DOI · Paper page
  70. 10.1002/jnr.490420411 · DOI
  71. 10.1006/bbrc.1995.2474 · DOI
  72. 10.1016/0960-8966(91)90059-2 · DOI
  73. 10.1136/jmg.30.9.737 · DOI
  74. 10.1126/science.270.5237.819 · DOI
  75. 10.1523/JNEUROSCI.14-03-01141.1994 · DOI
  76. 10.1093/hmg/2.11.1945 · DOI
  77. 10.1093/hmg/2.11.1765 · DOI
  78. 10.1016/0960-8966(94)00069-L · DOI
  79. 10.1038/ng0695-243 · DOI
  80. 10.1001/archopht.1993.01090110124037 · DOI
  81. 10.1038/ng0593-82 · DOI
  82. 10.1111/j.1432-0436.1992.tb00666.x · DOI
  83. 10.1002/ajmg.1320390414 · DOI
  84. 10.1016/0960-8966(92)90043-6 · DOI
  85. Roberds SL, 1993, Primary structure and muscle‐specific expression of the 50‐kDa dystrophin‐associated glycoprotein (adhalin), J Bio Chem, 268, 23739, 10.1016/S0021-9258(20)80440-2 · DOI
  86. 10.1016/0092-8674(94)90527-4 · DOI
  87. 10.1007/BF00267828 · DOI
  88. Shimmoto M., 1990, Atypical X‐linked muscular dystrophy with mental retardation: Analysis of a large deletion at the proximal region of dystrophin gene, Brain Dysfunct, 3, 72
  89. 10.1016/S0161-6420(13)31249-4 · DOI
  90. 10.1002/cne.902800203 · DOI
  91. 10.1002/jnr.490360505 · DOI
  92. 10.1074/jbc.270.25.15425 · DOI
  93. 10.1073/pnas.84.18.6457 · DOI
  94. 10.1111/j.1469-8749.1990.tb16978.x · DOI
  95. 10.1085/jgp.93.1.101 · DOI · Paper page
  96. 10.1016/0022-510X(93)90227-P · DOI
  97. 10.1073/pnas.91.18.8307 · DOI
  98. Tome FM, 1994, Congenital muscular dystrophy with merosin deficiency, Comptes Rendus de I Academie des Sciences Serie III, Sciences de la Vie, 317, 351
  99. 10.1002/jnr.490320114 · DOI
  100. 10.1093/brain/110.2.269 · DOI
  101. 10.1073/pnas.88.23.10764 · DOI
  102. 10.1007/BF00296181 · DOI
  103. 10.1136/jnnp.57.4.426 · DOI
  104. 10.1007/BF02327580 · DOI · Paper page
  105. 10.1111/j.1471-4159.1992.tb09421.x · DOI
  106. 10.1016/0014-5793(94)00917-1 · DOI
  107. 10.1093/oxfordjournals.jbchem.a124294 · DOI
  108. 10.1016/0022-510X(92)90054-O · DOI
  109. 10.1136/adc.55.8.589 · DOI
  110. 10.1016/0022-510X(94)90213-5 · DOI

Cited by

Sorted by citations

See all 110

Metadata

Authors
Lidov, H. G. W.
Affiliations
Boston Children's Hospital (US)
Corresponding author
Lidov, Hart G.W.
ORCID
Lidov, Hart G.W.
Venue
Brain Pathology
Publisher
Wiley
Published
1996-01
Volume
6
Issue
1
Pages
63-77
ISSN
  • 1015-6305 (ISSN-L)
  • 1750-3639
DOI
10.1111/j.1750-3639.1996.tb00783.x
OpenAlex
W1992269363
Cited by
110
References
0
Citations by year
2026: 1 · 2025: 3 · 2024: 1 · 2022: 2 · 2021: 7 · 2020: 3 · 2019: 3 · 2018: 6 · 2017: 4 · 2016: 7 · 2015: 3 · 2014: 1 · 2013: 2 · 2012: 7
FWCI
0.42
Type
journal article
Language
en
Open access
Licence
onlinelibrary.wiley.com/termsAndConditions#vor (vor, 4410 d)
Locations
  • Brain Pathology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • U.S. Public Health Service (KO801739-01)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Health Sciences › Medicine › Genetics (clinical) › Neurogenetic and Muscular Disorders Research
Keywords
dystrophin, Duchenne muscular dystrophy, cognitive function, nervous system
MeSH terms
Animals, Cognition, Heterozygote, Humans, Isomerism, Muscular Dystrophies, Nerve Tissue Proteins, Nervous System, Tissue Distribution, Dystrophin

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review