Human Molecular Genetics - Table of Contents
Volume 08, January - December 1999: Issue 05 -
Location at: http://www.oup.co.uk/hmg/Volume_08/Issue_05/
Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1
Yingzi Xue, Xiang Gao, Claire E. Lindsell, Christine R. Norton, Bo Chang, Carol Hicks, Maureen Gendron-Maguire1,p, Elizabeth B. Rand, Gerry Weinmaster and Thomas Gridley
Pages 723-730
Document ID = hmg_08_05_ddc089_gml
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Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone
David L. Stenoien, Chris J. Cummings, Henry P. Adams, Maureen G. Mancini, Kavita Patel, George N. DeMartino, Marco Marcelli, Nancy L. Weigel and Michael A. Mancini
Pages 731-741
Document ID = hmg_08_05_ddc091_gml
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Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)
Rando Allikmets, Wendy H. Raskind, Amy Hutchinson, Nichole D. Schueck, Michael Dean and David M. Koeller
Pages 743-749
Document ID = hmg_08_05_ddc101_gml
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Generation of an ~2.4 Mb human X centromere-based minichromosome by targeted telomere-associated chromosome fragmentation in DT40
Walter Mills, Ricky Critcher, Charles Lee and Christine J. Farr
Pages 751-761
Document ID = hmg_08_05_ddc106_gml
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A Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in mice
Peggy F. Shelbourne, Nigel Killeen, Robert F. Hevner, Heather M. Johnston, Laurence Tecott, Mark Lewandoski, Margaret Ennis, Lucia Ramirez, Zhen Li, Carlo Iannicola, Dan R. Littman and Richard M. Myers
Pages 763-774
Document ID = hmg_08_05_ddc104_gml
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The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution
Solange Bertrandy, Philippe Burlet, Olivier Clermont, Celine Huber, Christian Fondrat, Danielle Thierry-Mieg, Arnold Munnich and Suzie Lefebvre
Pages 775-782
Document ID = hmg_08_05_ddc102_gml
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A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
Michelle T. C. Jong, Todd A. Gray, Yonggang Ji, Christopher C. Glenn, Shinji Saitoh, Daniel J. Driscoll and Robert D. Nicholls
Pages 783-793
Document ID = hmg_08_05_ddc085_gml
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Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region
Michelle T. C. Jong, Alisoun H. Carey, Kim A. Caldwell, Michel H. Lau, Mary Ann Handel, Daniel J. Driscoll, Colin L. Stewart3,p, Eugene M. Rinchik and Robert D. Nicholls
Pages 795-803
Document ID = hmg_08_05_ddc084_gml
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Genome-wide scan for autism susceptibility genes
Anne Philippe, Maria Martinez, Michel Guilloud-Bataille, Christopher Gillberg, Maria Rastam, Eili Sponheim, Mary Coleman, Michele Zappella, Harald Aschauer, Lionel van Malldergerme, Christiane Penet, Josue Feingold, Alexis Brice, Marion Leboyer and the Paris Autism Research International Sibpair Study
Pages 805-812
Document ID = hmg_08_05_ddc098_gml
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Formation of polyglutamine inclusions in non-CNS tissue
Kirupa Sathasivam, Carl Hobbs, Mark Turmaine, Laura Mangiarini, Amarbirpal Mahal, Fabien Bertaux, Erich E. Wanker, Pat Doherty, Stephen W. Davies and Gillian P. Bates
Pages 813-822
Document ID = hmg_08_05_ddc092_gml
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Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium
Anna L. Millar, Tuya Pal, Lisa Madlensky, Chris Sherman, Larissa Temple, Angela Mitri, Hong Cheng, Victoria Marcus, Steven Gallinger, Mark Redston, Bharati Bapat and Steven Narod
Pages 823-829
Document ID = hmg_08_05_ddc100_gml
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Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out mice
J. E. Guidotti, A. Mignon, G. Haase, C. Caillaud, N. McDonell, A. Kahn and L. Poenaru
Pages 831-838
Document ID = hmg_08_05_ddc086_gml
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Impaired synaptic plasticity in mice carrying the Huntington's disease mutation
Martine T. Usdin, Peggy F. Shelbourne, Richard M. Myers and Daniel V. Madison
Pages 839-846
Document ID = hmg_08_05_ddc088_gml
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Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7
Joomyeong Kim, Xiaochen Lu and Lisa Stubbs
Pages 847-854
Document ID = hmg_08_05_ddc090_gml
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Dysferlin is a plasma membrane protein and is expressed early in human development
Louise V. B. Anderson, Keith Davison, Jennifer A. Moss, Carol Young, Michael J. Cullen, John Walsh, Margaret A. Johnson, Rumaisa Bashir, Stephen Britton, Sharon Keers, Zohar Argov, Ibrahim Mahjneh, Francoise Fougerousse, Jacques S. Beckmann and Kate M. D. Bushby
Pages 855-861
Document ID = hmg_08_05_ddc087_gml
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Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations
Filippo Tamanini, Carola Bontekoe, Cathy E. Bakker, Leontine van Unen, Burcu Anar, Rob Willemsen, Minoru Yoshida, Hans Galjaard, Ben A. Oostra and Andre T. Hoogeveen
Pages 863-869
Document ID = hmg_08_05_ddc094_gml
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Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)
Tracey Weiler, Rumaisa Bashir, Louise V. B. Anderson, Keith Davison, Jennifer A. Moss, Stephen Britton, Edward Nylen, Sharon Keers, Elizabeth Vafiadaki, Cheryl R. Greenberg, Kate M. D. Bushby and Klaus Wrogemann
Pages 871-877
Document ID = hmg_08_05_ddc107_gml
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Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7
Keiji Tamaki, Celia A. May, Yuri E. Dubrova and Alec J. Jeffreys
Pages 879-888
Document ID = hmg_08_05_ddc093_gml
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Germline BRCA1 alterations in a population-based series of ovarian cancer cases
Susan A. Janezic, Argyrios Ziogas, Lisa M. Krumroy, Meagan Krasner, Sarah J. Plummer, Patricia Cohen, Maureen Gildea, David Barker, Robert Haile, Graham Casey and Hoda Anton-Culver
Pages 889-897
Document ID = hmg_08_05_ddc096_gml
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Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
John H. Fingert, Elise Heon, Jeffrey M. Liebmann, Tetsuya Yamamoto, Jamie E. Craig, Julian Rait6, Kazuhide Kawase, Sek-Tien Hoh, Yvonne M. Buys, Joanne Dickinson, Robin R. Hockey, Donna Williams-Lyn, Graham Trope, Yoshiaki Kitazawa, Robert Ritch, David A. Mackey, Wallace L. M. Alward, Val C. Sheffield and Edwin M. Stone
Pages 899-905
Document ID = hmg_08_05_ddc095_gml
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Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy
Angela Netik, Sonja Forss-Petter, Andreas Holzinger, Brunhilde Molzer, Gertraud Unterrainer and Johannes Berger
Pages 907-913
Document ID = hmg_08_05_ddc103_gml
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DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children
Paul J. Fisher, Dragana Turic, Nigel M. Williams, Peter McGuffin, Philip Asherson, David Ball, Ian Craig, Thalia Eley, Linzy Hill, Karen Chorney, Michael J. Chorney, Camilla P. Benbow, David Lubinski, Robert Plomin and Michael J. Owen
Pages 915-922
Document ID = hmg_08_05_ddc097_gml
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Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21
Diana Hernandez, P. Joseph Mee, Joanne E. Martin, Victor L. J. Tybulewicz and Elizabeth M. C. Fisher
Pages 923-933
Document ID = hmg_08_05_ddc099_gml
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Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity
Stefano Colella, Tiziana Nardo, Donna Mallery, Carla Borrone, Roberta Ricci, Giuseppe Ruffa, Alan R. Lehmann and Miria Stefanini
Pages 935-941
Document ID = hmg_08_05_ddc105_gml
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Corrigenda
Pages 943-943
Document ID = hmg_08_05_corrigenda_gml
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