Human Molecular Genetics

ARTICLES:

Y Okamura-Oho, T Miyashita, K Ohmi, and M Yamada

Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate
Hum. Mol. Genet. 1999 8: 947-957; doi:10.1093/hmg/8.6.947 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

JP Venables, C Vernet, SL Chew, DJ Elliott, RB Cowmeadow, J Wu, HJ Cooke, K Artzt, and IC Eperon

T-STAR/ETOILE: a novel relative of SAM68 that interacts with an RNA- binding protein implicated in spermatogenesis
Hum. Mol. Genet. 1999 8: 959-969; doi:10.1093/hmg/8.6.959 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

L Rickman, D Simrak, HP Stevens, DM Hunt, IA King, SP Bryant, RA Eady, IM Leigh, J Arnemann, AI Magee, DP Kelsell, and RS Buxton

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma
Hum. Mol. Genet. 1999 8: 971-976; doi:10.1093/hmg/8.6.971 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

M Waragai, CH Lammers, S Takeuchi, I Imafuku, Y Udagawa, I Kanazawa, M Kawabata, MM Mouradian, and H Okazawa

PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival
Hum. Mol. Genet. 1999 8: 977-987; doi:10.1093/hmg/8.6.977 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

CS Raymond, ED Parker, JR Kettlewell, LG Brown, DC Page, K Kusz, J Jaruzelska, Y Reinberg, WL Flejter, VJ Bardwell, B Hirsch, and D Zarkower

A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators
Hum. Mol. Genet. 1999 8: 989-996; doi:10.1093/hmg/8.6.989 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

A Sato, T Shimohata, R Koide, H Takano, T Sato, M Oyake, S Igarashi, K Tanaka, T Inuzuka, H Nawa, and S Tsuji

Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis
Hum. Mol. Genet. 1999 8: 997-1006; doi:10.1093/hmg/8.6.997 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

J Lightfoot, N Alon, L Bosnoyan-Collins, and M Buchwald

Characterization of regions functional in the nuclear localization of the Fanconi anemia group A protein
Hum. Mol. Genet. 1999 8: 1007-1015; doi:10.1093/hmg/8.6.1007 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Z Korade-Mirnics, J Tarleton, S Servidei, RR Casey, M Gennarelli, E Pegoraro, C Angelini, and EP Hoffman

Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression
Hum. Mol. Genet. 1999 8: 1017-1023; doi:10.1093/hmg/8.6.1017 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

SL Christian, JA Fantes, SK Mewborn, B Huang, and DH Ledbetter

Large genomic duplicons map to sites of instability in the Prader- Willi/Angelman syndrome chromosome region (15q11-q13)
Hum. Mol. Genet. 1999 8: 1025-1037; doi:10.1093/hmg/8.6.1025 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

L Zurutuza, F Muller, JF Gibrat, A Taillandier, B Simon-Bouy, JL Serre, and E Mornet

Correlations of genotype and phenotype in hypophosphatasia
Hum. Mol. Genet. 1999 8: 1039-1046; doi:10.1093/hmg/8.6.1039 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

T Taivassalo, K Fu, T Johns, D Arnold, G Karpati, and EA Shoubridge

Gene shifting: a novel therapy for mitochondrial myopathy
Hum. Mol. Genet. 1999 8: 1047-1052; doi:10.1093/hmg/8.6.1047 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

M Eriksson, T Ansved, L Edstrom, M Anvret, and N Carey

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
Hum. Mol. Genet. 1999 8: 1053-1060; doi:10.1093/hmg/8.6.1053 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

GJ Brock, NH Anderson, and DG Monckton

Cis-acting modifiers of expanded CAG/CTG triplet repeat expandability: associations with flanking GC content and proximity to CpG islands
Hum. Mol. Genet. 1999 8: 1061-1067; doi:10.1093/hmg/8.6.1061 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

S La Fontaine, SD Firth, PJ Lockhart, H Brooks, J Camakaris, and JF Mercer

Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants
Hum. Mol. Genet. 1999 8: 1069-1075; doi:10.1093/hmg/8.6.1069 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

N Shimozawa, Y Suzuki, Z Zhang, A Imamura, R Toyama, S Mukai, Y Fujiki, T Tsukamoto, T Osumi, T Orii, RJ Wanders, and N Kondo

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders
Hum. Mol. Genet. 1999 8: 1077-1083; doi:10.1093/hmg/8.6.1077 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

SM Gartler, L Goldstein, SE Tyler-Freer, and RS Hansen

The timing of XIST replication: dominance of the domain
Hum. Mol. Genet. 1999 8: 1085-1089; doi:10.1093/hmg/8.6.1085 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

I Jarvela, M Lehtovirta, R Tikkanen, A Kyttala, and A Jalanko

Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)
Hum. Mol. Genet. 1999 8: 1091-1098; doi:10.1093/hmg/8.6.1091 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

SS Branda, ZY Yang, A Chew, and G Isaya

Mitochondrial intermediate peptidase and the yeast frataxin homolog together maintain mitochondrial iron homeostasis in Saccharomyces cerevisiae
Hum. Mol. Genet. 1999 8: 1099-1110; doi:10.1093/hmg/8.6.1099 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

SA Igdoura, C Mertineit, JM Trasler, and RA Gravel

Sialidase-mediated depletion of GM2 ganglioside in Tay-Sachs neuroglia cells
Hum. Mol. Genet. 1999 8: 1111-1116; doi:10.1093/hmg/8.6.1111 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

H Hao, LE Morrison, and CT Moraes

Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background
Hum. Mol. Genet. 1999 8: 1117-1124; doi:10.1093/hmg/8.6.1117 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

L Riou, L Zeng, O Chevallier-Lagente, A Stary, O Nikaido, A Taieb, G Weeda, M Mezzina, and A Sarasin

The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes
Hum. Mol. Genet. 1999 8: 1125-1133; doi:10.1093/hmg/8.6.1125 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

R Tazi Ahnini, NJ Camp, MJ Cork, JB Mee, SG Keohane, GW Duff, and FS di Giovine

Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis
Hum. Mol. Genet. 1999 8: 1135-1140; doi:10.1093/hmg/8.6.1135 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

CORRIGENDUM:

Corrigendum
Hum. Mol. Genet. 1999 8: 1141; doi:10.1093/hmg/8.6.1141 [PDF] [Request Permissions]  

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