Gene shifting: a novel therapy for mitochondrial myopathy.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1047, doi. 10.1093/hmg/8.6.1047
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 1999 AND VI 8 AND IP 6
Results: 22
1
2
A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 989, doi. 10.1093/hmg/8.6.989
- By:
- Publication type:
- Article
3
Sialidase-mediated depletion of G[sub m2] ganglioside in Tay-Sachs neuroglia cells.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1111, doi. 10.1093/hmg/8.6.1111
- By:
- Publication type:
- Article
4
Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 947, doi. 10.1093/hmg/8.6.947
- By:
- Publication type:
- Article
5
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1017, doi. 10.1093/hmg/8.6.1017
- By:
- Publication type:
- Article
6
Characterization of regions functional in the nuclear localization of the Fanconi anemia group A protein.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1007, doi. 10.1093/hmg/8.6.1007
- By:
- Publication type:
- Article
7
Cis-acting modifiers of expanded CAG/CTG triplet repeat expandability: associations with flanking GC content and proximity to CpG islands.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1061, doi. 10.1093/hmg/8.6.1061
- By:
- Publication type:
- Article
8
Correlations of genotype and phenotype in hypophosphatasia.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1039, doi. 10.1093/hmg/8.6.1039
- By:
- Publication type:
- Article
9
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 971, doi. 10.1093/hmg/8.6.971
- By:
- Publication type:
- Article
10
T-STAR/ETOILE: a novel relative of SAM68 that interacts with an RNA-binding protein implicated in spermatogenesis.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 959, doi. 10.1093/hmg/8.6.959
- By:
- Publication type:
- Article
11
Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL).
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1091, doi. 10.1093/hmg/8.6.1091
- By:
- Publication type:
- Article
12
Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1053, doi. 10.1093/hmg/8.6.1053
- By:
- Publication type:
- Article
13
Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 997, doi. 10.1093/hmg/8.6.997
- By:
- Publication type:
- Article
14
Mitochondrial intermediate peptidase and the yeast frataxin homolog together maintain mitochondrial iron homeostasis in Saccharomyces cerevisiae.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1099, doi. 10.1093/hmg/8.6.1099
- By:
- Publication type:
- Article
15
Intracellular localization and loss of copper responsiveness on Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo [sup blo]) and brindled (Mo [sup br]) mouse mutants.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1069, doi. 10.1093/hmg/8.6.1069
- By:
- Publication type:
- Article
16
The timing of XIST replication: dominance of the domain.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1085, doi. 10.1093/hmg/8.6.1085
- By:
- Publication type:
- Article
17
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1077, doi. 10.1093/hmg/8.6.1077
- By:
- Publication type:
- Article
18
The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1125, doi. 10.1093/hmg/8.6.1125
- By:
- Publication type:
- Article
19
PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activitation by Brn-2 and affects cell survival.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 977, doi. 10.1093/hmg/8.6.977
- By:
- Publication type:
- Article
20
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1025, doi. 10.1093/hmg/8.6.1025
- By:
- Publication type:
- Article
21
\Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1117, doi. 10.1093/hmg/8.6.1117
- By:
- Publication type:
- Article
22
Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 6, p. 1135, doi. 10.1093/hmg/8.6.1135
- By:
- Publication type:
- Article