Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 21
Results: 21
Obesity, hyperphagia and increased metabolic efficiency in Pc1 mutant mice.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3435, doi. 10.1093/hmg/ddn254
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- Article
Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3332, doi. 10.1093/hmg/ddn228
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- Article
Subscription Page.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. NP, doi. 10.1093/hmg/ddn330
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- Article
Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3271, doi. 10.1093/hmg/ddn223
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- Article
Contents Page.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. NP, doi. 10.1093/hmg/ddn331
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- Article
Human neural crest cells display molecular and phenotypic hallmarks of stem cells.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3411, doi. 10.1093/hmg/ddn235
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- Article
Cover Page.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. NP, doi. 10.1093/hmg/ddn328
- Publication type:
- Article
Analysis of genome-wide copy number variation in Irish and Dutch ALS populations.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3392, doi. 10.1093/hmg/ddn233
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- Article
A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3426, doi. 10.1093/hmg/ddn236
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- Article
Edar and Troy signalling pathways act redundantly to regulate initiation of hair follicle development.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3380, doi. 10.1093/hmg/ddn232
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- Article
A high-density association screen of 155 ion transport genes for involvement with common migraine.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3318, doi. 10.1093/hmg/ddn227
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- Article
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3436, doi. 10.1093/hmg/ddn259
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- Article
Editorial Board.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. NP, doi. 10.1093/hmg/ddn329
- Publication type:
- Article
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3291, doi. 10.1093/hmg/ddn225
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- Article
Different regulation of wild-type and mutant Cu,Zn superoxide dismutase localization in mammalian mitochondria.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3303, doi. 10.1093/hmg/ddn226
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- Article
Targeted disruption of Nphp1 causes male infertility due to defects in the later steps of sperm morphogenesis in mice.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3368, doi. 10.1093/hmg/ddn231
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- Article
Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3263, doi. 10.1093/hmg/ddn222
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- Article
Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3340, doi. 10.1093/hmg/ddn229
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- Article
Synergistic activation of the human MnSOD promoter by DJ-1 and PGC-1α: regulation by SUMOylation and oxidation.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3357, doi. 10.1093/hmg/ddn230
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- Article
Mice deficient for the chromosome 21 ortholog Itsn1 exhibit vesicle-trafficking abnormalities.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3281, doi. 10.1093/hmg/ddn224
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- Article
SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain.
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- Human Molecular Genetics, 2008, v. 17, n. 21, p. 3399, doi. 10.1093/hmg/ddn234
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- Article