IGF2 is parentally imprinted in human preimplantation embryospp122 - 123 Antony D. Lighten, Kate Hardy, Robert M.L. Winston
& Gudrun E. Moore doi:10.1038/ng0297-122 References|PDF
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Cholesterol, hedgehog and embryogenesispp123 - 124 Joachim Herz, Thomas E. Willnow
& Robert V. Farese Jr doi:10.1038/ng0297-123 References|PDF
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International collaboration in genetics researchp124 Somnath Chatterji, Sanjeev Jain, Samir K. Brahmachari, Partha Majumder
& Theodore Reich doi:10.1038/ng0297-124 References|PDF
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A human candidate spermatogenesis gene, RBM1, is conserved and amplified on the marsupial Y chromosomepp131 - 136 Margaret L. Delbridge, Jenny L. Harry, Roland Toder, Rachel J. Waugh O'Neill, Kun Ma, Ann C. Chandley
& Jennifer A. Marshall Graves doi:10.1038/ng0297-131 Abstract + references|PDF
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Complete inventory of the yeast ABC proteinspp137 - 145 Anabelle Decottignies
& André Goffeau doi:10.1038/ng0297-137 Abstract + references|PDF
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Functional transplant of megabase human immunoglobulin loci recapitulates human antibody response in micepp146 - 156 Michael J. Mendez, Larry L. Green, Jose R.F. Corvalan, Xiao-Chi Jia, Catherine E. Maynard-Currie, Xiao-dong Yang, Michael L. Gallo, Donna M. Louie, Doris V. Lee, Karen L. Erickson, Jac Luna, Catherine M.-N. Roy, Hadi Abderrahim, Ford Kirschenbaum, Masato Noguchi, Douglas H. Smith, Atsushi Fukushima, Joanna F. Hales, Mitchell H. Finer, C. Geoffrey Davis, Krisztina M. Zsebo
& Aya Jakobovits doi:10.1038/ng0297-146 Abstract + references|PDF
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A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene familypp157 - 164 Sonia Abdelhak, Vasiliki Kalatzis, Roland Heilig, Sylvie Compain, Delphine Samson, Christophe Vincent, Dominique Weil, Corinne Cruaud, Iman Sahly, Michel Leibovici, Maria Bitner-Glindzicz, Mary Francis, Didier Lacombe, Jacqueline Vigneron, Robert Charachon, Katia Boven, Philippe Bedbeder, Nicole Van Regemorter, Jean Weissenbach
& Christine Petit doi:10.1038/ng0297-157 Abstract + references|PDF
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Characterization of the full fragile X syndrome mutation in fetal gametespp165 - 169 Henry E. Malter, Jane C. Iber, R. Willemsen, Esther de Graaff, Jack C. Tarleton, J. Leisti, Stephen T. Warren
& Ben A. Oostra doi:10.1038/ng0297-165 Abstract + references|PDF
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Promoter swapping between the genes for a novel zinc finger protein and -catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocationspp170 - 174 Koen Kas, Marianne L. Voz, Eva Röijer, Anna-Karin Åström, Eva Meyen, Göran Stenman
& Wim J.M. Van de Ven doi:10.1038/ng0297-170 Abstract + references|PDF
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Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindnesspp175 - 178 Shuji Yamamoto, Kimberly C. Sippel, Eliot L. Berson
& Thaddeus P. Dryja doi:10.1038/ng0297-175 Abstract + references|PDF
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Mutation of HOXA13 in hand-foot-genital syndrome
pp179 - 180 Douglas P. Mortlock
& Jeffrey W. Innis doi:10.1038/ng0297-179 Abstract + references|PDF
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Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangementspp181 - 185 Maxwell P. Lee, Ren-JuHu Hu, Laura A. Johnson
& Andrew P. Feinberg doi:10.1038/ng0297-181 Abstract + references|PDF
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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromepp186 - 189 Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy, Michel Leibovici, Claire Donger, Jacques Barhanin, Sabine Fauré, Françoise Gary, Philippe Coumel, Christine Petit, Ketty Schwartz
& Pascale Guicheney doi:10.1038/ng0297-186 Abstract + references|PDF
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Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic micepp190 - 192 Geneviève Gourdon, François Radvanyi, Anne-Sophie Lia, Chantal Duros, Martine Blanche, Marc Abitbol, Claudine Junien
& Hlène Hofmann-Radvanyi doi:10.1038/ng0297-190 Abstract + references|PDF
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Hypermutable myotonic dystrophy CTG repeats in transgenic micepp193 - 196 Darren G. Monckton, Mary I. Coolbaugh, Ken T. Ashizawa, Michael J. Siciliano
& C. Thomas Caskey doi:10.1038/ng0297-193 Abstract + references|PDF
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Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutationpp197 - 200 Laura Mangiarini, Kirupa Sathasivam, Amarbirpal Mahal, Richard Mott, Mary Seller
& Gillian P. Bates doi:10.1038/ng0297-197 Abstract + references|PDF
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Follicle stimulating hormone is required for ovarian follicle maturation but not male fertilitypp201 - 204 T. Rajendra Kumar, Yan Wang, Naifang Lu
& Martin M. Matzuk doi:10.1038/ng0297-201 Abstract + references|PDF
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Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertilitypp205 - 206 Juha S. Tapanainen, Kristiina Aittomäki, Jiang Min, Tommi Vaskivuo
& Ilpo T. Huhtaniemi doi:10.1038/ng0297-205 Abstract + references|PDF
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Mapping of a major genetic modifier of embryonic lethality in TGF1 knockout micepp207 - 211 Mortaza Bonyadi, Sarah A.B. Rusholme, Frances M. Cousins, Helen C. Su, Christine A. Biron, Martin Farrall
& Rosemary J. Akhurst doi:10.1038/ng0297-207 Abstract + references|PDF
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Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acidspp212 - 215 Robert W. Taylor, Patrick F. Chinnery, Douglass M. Turnbull
& Robert N. Lightowlers doi:10.1038/ng0297-212 Abstract + references|PDF
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Retinopathy induced in mice by targeted disruption of the rhodopsin genepp216 - 219 Marian M. Humphries, Derrick Rancourt, G. Jane Farrar, Paul Kenna, Mark Hazel, Ronald A. Bush, Paul A. Sieving, Denise M. Sheils, Peter Creighton, Alexandra Erven, Andras Boros, Karoly Gulya, Mario R. Capecchi
& Peter Humphries doi:10.1038/ng0297-216 Abstract + references|PDF
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-catenin in pleiomorphic adenomas with t(3;8)(p21;q12) translocations
