Works matching IS 09646906 AND DT 2019 AND VI 28 AND IP 24
Results: 14
Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4161, doi. 10.1093/hmg/ddz263
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- Article
Methylation changes in the peripheral blood of Filipinos with type 2 diabetes suggest spurious transcription initiation at TXNIP.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4208, doi. 10.1093/hmg/ddz262
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- Article
Splicing factor DHX15 affects tp53 and mdm2 expression via alternate splicing and promoter usage.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4173, doi. 10.1093/hmg/ddz261
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- Article
Insights into wild-type dynamin 2 and the consequences of DNM2 mutations from transgenic zebrafish.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4186, doi. 10.1093/hmg/ddz260
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- Article
Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4089, doi. 10.1093/hmg/ddz254
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- Article
BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4148, doi. 10.1093/hmg/ddz252
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- Article
Different in vivo impacts of dynamin 2 mutations implicated in Charcot–Marie–Tooth neuropathy or centronuclear myopathy.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4067, doi. 10.1093/hmg/ddz249
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- Article
PRCD is concentrated at the base of photoreceptor outer segments and is involved in outer segment disc formation.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4078, doi. 10.1093/hmg/ddz248
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- Article
The consequences of increased 4E-BP1 in polycystic kidney disease.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4132, doi. 10.1093/hmg/ddz244
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- Article
A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4197, doi. 10.1093/hmg/ddz243
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- Article
Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4103, doi. 10.1093/hmg/ddz240
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- Article
Long-term environmental impact on object recognition, spatial memory and reversal learning capabilities in Cacna1c-haploinsufficient rats.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4113, doi. 10.1093/hmg/ddz235
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- Article
ADAMTS9 and ADAMTS20 are differentially affected by loss of B3GLCT in mouse model of Peters plus syndrome.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4053, doi. 10.1093/hmg/ddz225
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- Article
Microtubule cytoskeleton regulates Connexin 43 localization and cardiac conduction in cardiomyopathy caused by mutation in A-type lamins gene.
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- Human Molecular Genetics, 2019, v. 28, n. 24, p. 4043, doi. 10.1093/hmg/ddy227
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- Article