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Table of contents of journal: *Human molecular genetics (Print)

Results: 1-25/313

Authors: Araishi, K Sasaoka, T Imamura, M Noguchi, S Hama, H Wakabayashi, E Yoshida, M Hori, T Ozawa, E
Citation: K. Araishi et al., Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice, HUM MOL GEN, 8(9), 1999, pp. 1589-1598

Authors: Horesh, D Sapir, T Francis, F Wolf, SG Caspi, M Elbaum, M Chelly, J Reiner, O
Citation: D. Horesh et al., Doublecortin, a stabilizer of microtubules, HUM MOL GEN, 8(9), 1999, pp. 1599-1610

Authors: Sakuntabhai, A Burge, S Monk, S Hovnanian, A
Citation: A. Sakuntabhai et al., Spectrum of novel ATP2A2 mutations in patients with Darier's disease, HUM MOL GEN, 8(9), 1999, pp. 1611-1619

Authors: Ruiz-Perez, VL Carter, SA Healy, E Todd, C Rees, JL Steijlen, PM Carmichael, AJ Lewis, HM Hohl, D Itin, P Vahlquist, A Gobello, T Mazzanti, C Reggazini, R Nagy, G Munro, CS Strachan, T
Citation: Vl. Ruiz-perez et al., ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class, HUM MOL GEN, 8(9), 1999, pp. 1621-1630

Authors: Jacobsen, NJO Lyons, I Hoogendoorn, B Burge, S Kwok, PY O'Donovan, MC Craddock, N Owen, MJ
Citation: Njo. Jacobsen et al., ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes, HUM MOL GEN, 8(9), 1999, pp. 1631-1636

Authors: Coleman, J Baird, DM Royle, NJ
Citation: J. Coleman et al., The plasticity of human telomeres demonstrated by a hypervariable telomererepeat array that is located on some copies of 16p and 16q, HUM MOL GEN, 8(9), 1999, pp. 1637-1646

Authors: Boutell, JM Thomas, P Neal, JW Weston, VJ Duce, J Harper, PS Jones, AL
Citation: Jm. Boutell et al., Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin, HUM MOL GEN, 8(9), 1999, pp. 1647-1655

Authors: Kaytor, MD Duvick, LA Skinner, PJ Koob, MD Ranum, LPW Orr, HT
Citation: Md. Kaytor et al., Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7, HUM MOL GEN, 8(9), 1999, pp. 1657-1664

Authors: Buiakova, OI Xu, J Lutsenko, S Zeitlin, S Das, K Das, S Ross, BM Mekios, C Scheinberg, IH Gilliam, TC
Citation: Oi. Buiakova et al., Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation, HUM MOL GEN, 8(9), 1999, pp. 1665-1671

Authors: Toyama, R Mukai, S Itagaki, A Tamura, S Shimozawa, N Suzuki, Y Kondo, N Wanders, RJA Fujiki, Y
Citation: R. Toyama et al., Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants, HUM MOL GEN, 8(9), 1999, pp. 1673-1681

Authors: Odent, S Attie-Bitach, T Blayau, M Mathieu, M Auge, J Delezoide, AL Le Gall, JY Le Marec, B Munnich, A David, V Vekemans, M
Citation: S. Odent et al., Expression of the Sonic hedgehog (SHH) gene during early human developmentand phenotypic expression of new mutations causing holoprosencephaly, HUM MOL GEN, 8(9), 1999, pp. 1683-1689

Authors: Williams, AJ Murrell, M Brammah, S Minchenko, J Christodoulou, J
Citation: Aj. Williams et al., A novel system for assigning the mode of inheritance in mitochondrial disorders using cybrids and rhodamine 6G, HUM MOL GEN, 8(9), 1999, pp. 1691-1697

Authors: Yip, SP Lovegrove, JU Rana, NA Hopkinson, DA Whitehouse, DB
Citation: Sp. Yip et al., Mapping recombination hotspots in human phosphoglucomutase (PGM1), HUM MOL GEN, 8(9), 1999, pp. 1699-1706

Authors: Cox, A Camp, NJ Cannings, C di Giovine, FS Dale, M Worthington, J John, S Ollier, WER Silman, AJ Duff, GW
Citation: A. Cox et al., Combined sib-TDT and TDT provide evidence for linkage of the interleukin-1gene cluster to erosive rheumatoid arthritis, HUM MOL GEN, 8(9), 1999, pp. 1707-1713

Authors: Bertucci, F Bernard, K Loriod, B Chang, YC Granjeaud, S Birnbaum, D Nguyen, C Peck, K Jordan, BR
Citation: F. Bertucci et al., Sensitivity issues in DNA array-based expression measurements and performance of nylon microarrays for small samples, HUM MOL GEN, 8(9), 1999, pp. 1715-1722

Authors: Donnelly, SR Hawkins, TE Moss, SE
Citation: Sr. Donnelly et al., A conserved nuclear element with a role in mammalian gene regulation, HUM MOL GEN, 8(9), 1999, pp. 1723-1728

Authors: Williams, NM Rees, MI Holmans, P Norton, N Cardno, AG Jones, LA Murphy, KC Sanders, RD McCarthy, G Gray, MY Fenton, I McGuffin, P Owen, MJ
Citation: Nm. Williams et al., A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs, HUM MOL GEN, 8(9), 1999, pp. 1729-1739

Authors: Arnould, C Philippe, C Bourdon, V Gregoire, MJ Berger, R Jonveaux, P
Citation: C. Arnould et al., The signal transducer and activator of transcription STAT5b gene is a new partner of retinoic acid receptor alpha in acute promyelocytic-like leukaemia, HUM MOL GEN, 8(9), 1999, pp. 1741-1749

Authors: Vergani, L Rossi, R Brierley, CH Hanna, N Holt, IJ
Citation: L. Vergani et al., Introduction of heteroplasmic mitochondrial DNA (mtDNA) from a patient with NARP into two human rho degrees cell lines is associated either with selection and maintenance of NARP mutant mtDNA or failure to maintain mtDNA, HUM MOL GEN, 8(9), 1999, pp. 1751-1755

Authors: Pilz, DT Kuc, J Matsumoto, N Bodurtha, J Bernadi, B Tassinari, CA Dobyns, WB Ledbetter, DH
Citation: Dt. Pilz et al., Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1, HUM MOL GEN, 8(9), 1999, pp. 1757-1760

Authors: Ikeda, A Zheng, QY Rosenstiel, P Maddatu, T Zuberi, AR Roopenian, DC North, MA Naggert, JK Johnson, KR Nishina, PM
Citation: A. Ikeda et al., Genetic modification of heaving in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss, HUM MOL GEN, 8(9), 1999, pp. 1761-1767

Authors: Kalff-Suske, M Wild, A Topp, J Wessling, M Jacobsen, EM Bornholdt, D Engel, H Heuer, H Aalfs, CM Ausems, MGEM Barone, R Herzog, A Heutink, P Homfray, T Gillessen-Kaesbach, G Konig, R Kunze, J Meinecke, P Muller, D Rizzo, R Strenge, S Superti-Furga, A Grzeschik, KH
Citation: M. Kalff-suske et al., Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactylysyndrome, HUM MOL GEN, 8(9), 1999, pp. 1769-1777

Authors: Grewal, RP Cancel, G Leeflang, EP Durr, A McPeek, MS Draghinas, D Yao, X Stevanin, G Alnot, MO Brice, A Arnheim, N
Citation: Rp. Grewal et al., French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysis, HUM MOL GEN, 8(9), 1999, pp. 1779-1784

Authors: Bondurand, N Kuhlbrodt, K Pingault, V Enderich, J Sajus, M Tommerup, N Warburg, M Hennekam, RCM Read, AP Wegner, M Goossens, N
Citation: N. Bondurand et al., A molecular analysis of the Yemenite deaf-blind hypopigmentation syndrome:SOX10 dysfunction causes different neurocristopathies, HUM MOL GEN, 8(9), 1999, pp. 1785-1789

Authors: Lalioti, MD Scott, HS Antonarakis, SE
Citation: Md. Lalioti et al., Altered spacing of promoter elements due to the dodecamer repeat expansioncontributes to reduced expression of the cystatin B gene in EPM1, HUM MOL GEN, 8(9), 1999, pp. 1791-1798
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