Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16–17.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 2978, doi. 10.1093/hmg/ddy197
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2018 AND VI 27 AND IP 17
Results: 12
1
2
The presenilin loop region is essential for glycogen synthase kinase 3 β (GSK3β) mediated functions on motor proteins during axonal transport.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 2986, doi. 10.1093/hmg/ddy190
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- Publication type:
- Article
3
Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich’s ataxia patients.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 2965, doi. 10.1093/hmg/ddy198
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- Publication type:
- Article
4
Loss of 5hmC identifies a new type of aberrant DNA hypermethylation in glioma.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3046, doi. 10.1093/hmg/ddy214
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- Publication type:
- Article
5
Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3029, doi. 10.1093/hmg/ddy213
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- Publication type:
- Article
6
Improvement of BDNF signalling by P42 peptide in Huntington's disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3012, doi. 10.1093/hmg/ddy207
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- Publication type:
- Article
7
Consortium-based genome-wide meta-analysis for childhood dental caries traits.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3113, doi. 10.1093/hmg/ddy237
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- Publication type:
- Article
8
A collective diabetes cross in combination with a computational framework to dissect the genetics of human obesity and Type 2 diabetes.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3099, doi. 10.1093/hmg/ddy217
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- Publication type:
- Article
9
Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3060, doi. 10.1093/hmg/ddy215
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- Publication type:
- Article
10
Antioxidant treatment ameliorates phenotypic features of SMC1A-mutated Cornelia de Lange syndrome in vitro and in vivo.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3002, doi. 10.1093/hmg/ddy203
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- Publication type:
- Article
11
AAV9 intracerebroventricular gene therapy improves lifespan, locomotor function and pathology in a mouse model of Niemann–Pick type C1 disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3079, doi. 10.1093/hmg/ddy212
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- Publication type:
- Article
12
5-Hydroxymethylcytosine alterations in the human postmortem brains of autism spectrum disorder.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 17, p. 2955, doi. 10.1093/hmg/ddy193
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- Publication type:
- Article