Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 520, doi. 10.1093/hmg/ddad203
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- Publication type:
- Article
Works matching IS 09646906 AND DT 2024 AND VI 33 AND IP 6
Results: 8
1
2
Long term peripheral AAV9-SMN gene therapy promotes survival in a mouse model of spinal muscular atrophy.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 510, doi. 10.1093/hmg/ddad202
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- Publication type:
- Article
3
Comprehensive whole-genome analyses of the UK Biobank reveal significant sex differences in both genotype missingness and allele frequency on the X chromosome.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 543, doi. 10.1093/hmg/ddad201
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- Publication type:
- Article
4
Editor's Note on 'ZZ domain is essentially required for the physiological binding of dystrophin and utrophin to β-dystroglycan'.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 477, doi. 10.1093/hmg/ddad200
- Publication type:
- Article
5
ALS iPSC-derived microglia and motor neurons respond to astrocyte-targeted IL-10 and CCL2 modulation.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 530, doi. 10.1093/hmg/ddad209
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- Publication type:
- Article
6
Subtyping and prognostic model construction based on vesicle-mediated transport-related genes in colorectal cancer.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 478, doi. 10.1093/hmg/ddad197
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- Publication type:
- Article
7
Ovol2 promoter mutations in mice and human illuminate species-specific phenotypic divergence.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 491, doi. 10.1093/hmg/ddad195
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- Publication type:
- Article
8
Epigenomic profiling of the infrapatellar fat pad in osteoarthritis.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 6, p. 501, doi. 10.1093/hmg/ddad198
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- Publication type:
- Article