Works matching IS 09646906 AND DT 2002 AND VI 11 AND IP 6
Results: 12
The expression of a new variant of the pro-apoptotic molecule Bax, Baxψ, is correlated with an increased survival of glioblastoma multiforme patients.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 6, p. 675, doi. 10.1093/hmg/11.6.675
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- Article
Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 715, doi. 10.1093/hmg/11.6.715
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- Article
WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 651, doi. 10.1093/hmg/11.6.651
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- Article
Sequence dependent instability of mononucleotide microsatellites in cultured mismatch repair proficient and deficient mammalian cells.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 707, doi. 10.1093/hmg/11.6.707
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- Article
Linkage analysis of anorexia nervosa incorporating behavioral covariates.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 689, doi. 10.1093/hmg/11.6.689
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- Article
The gene for the muted (mu) mouse, a model for Hermansky–Pudlak syndrome, defines a novel protein which regulates vesicle trafficking.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 697, doi. 10.1093/hmg/11.6.697
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- Article
Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 641, doi. 10.1093/hmg/11.6.641
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- Article
STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 613, doi. 10.1093/hmg/11.6.613
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- Article
Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 633, doi. 10.1093/hmg/11.6.633
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- Article
Classification of common conserved sequences in mammalian intergenic regions.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 669, doi. 10.1093/hmg/11.6.669
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- Article
Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 623, doi. 10.1093/hmg/11.6.623
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- Article
Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3–p32.2.
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- Human Molecular Genetics, 2002, v. 11, n. 6, p. 661, doi. 10.1093/hmg/11.6.661
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- Article