Found: 16
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Mutation of a transcriptional motif of a distant regulatory element reduces the expression of embryonic and fetal globin genes.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2941, doi. 10.1093/hmg/ddg319
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- Publication type:
- Article
NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid droplets.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2981, doi. 10.1093/hmg/ddg321
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- Publication type:
- Article
Interaction between a peroxisome proliferator-activated receptor γ gene polymorphism and dietary fat intake in relation to body mass.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2923, doi. 10.1093/hmg/ddg318
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- Article
The HLA class III subregion is responsible for an increased breast cancer risk.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 3041, doi. 10.1093/hmg/ddg342
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- Article
Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2967, doi. 10.1093/hmg/ddg329
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- Publication type:
- Article
RING finger 1 mutations in Parkin produce altered localization of the protein.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2957, doi. 10.1093/hmg/ddg328
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- Publication type:
- Article
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2895, doi. 10.1093/hmg/ddg327
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- Publication type:
- Article
Gene expression variation in the adult human retina.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2881, doi. 10.1093/hmg/ddg326
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- Article
Inducible mEDA-A1 transgene mediates sebaceous gland hyperplasia and differential formation of two types of mouse hair follicles.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2931, doi. 10.1093/hmg/ddg325
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- Publication type:
- Article
Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.
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- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2993, doi. 10.1093/hmg/ddg324
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- Publication type:
- Article
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2909, doi. 10.1093/hmg/ddg323
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- Publication type:
- Article
Genetic background regulates β-amyloid precursor protein processing and β-amyloid deposition in the mouse.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2949, doi. 10.1093/hmg/ddg322
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- Publication type:
- Article
Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 3017, doi. 10.1093/hmg/ddg320
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- Publication type:
- Article
Co-duplication of olfactory receptor and MHC class I genes in the mouse major histocompatibility complex.
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- Human Molecular Genetics, 2003, v. 12, n. 22, p. 3025, doi. 10.1093/hmg/ddg317
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- Publication type:
- Article
E-cadherin germline missense mutations and cell phenotype: evidence for the independence of cell invasion on the motile capabilities of the cells.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 3007, doi. 10.1093/hmg/ddg316
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- Publication type:
- Article
Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 22, p. 2873, doi. 10.1093/hmg/ddg315
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- Publication type:
- Article