TSG101 may be the prototype of a class of dominant negative ubiquitin regulatorspp330 - 331 Eugene V. Koonin
& Ruben A. Abagyan doi:10.1038/ng0897-330 References|PDF
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Absence of rearrangements in the tumour susceptibility gene TSG101 in human breast cancerpp332 - 333 Philipp Steiner, Diana M. Barnes, William H. Harris
& Robert A. Weinberg doi:10.1038/ng0897-332 References|PDF
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Germline mutations in PTEN are present in Bannayan-Zonana syndromepp333 - 334 Debbie J. Marsh, Patricia L. M. Dahia, Zimu Zheng, Danny Liaw, Ramon Parsons, Robert J. Gorlin
& Charis Eng doi:10.1038/ng0897-333 References|PDF
(333K)
Impaired nuclear localization of defective DNA helicases in Werner's syndromepp335 - 336 Takehisa Matsumoto, Akira Shimamoto, Makoto Goto
& Yasuhiro Furuichi doi:10.1038/ng0897-335 References|PDF
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Deletion of p21 cannot substitute for p53 loss in rescue of mdm2 null lethalitypp336 - 337 Roberto Montes de Oca Luna, Lisa L. Amelse, Arturo Chavez-Reyes, Susan C. Evans, James Brugarolas, Tyler Jacks
& Guillermina Lozano doi:10.1038/ng0897-336 References|PDF
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Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxinpp345 - 351 Hana Koutnikova, Victoria Campuzano, Françoise Foury, Pascal Dollé, Ornella Cazzalini
& Michel Koenig doi:10.1038/ng0897-345 Abstract + references|PDF
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Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologuepp352 - 357 Robert B. Wilson
& David M. Roof doi:10.1038/ng0897-352 Abstract + references|PDF
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Bcl-2 and Bax function independently to regulate cell deathpp358 - 363 C. Michael Knudson
& Stanley J. Korsmeyer doi:10.1038/ng0897-358 Abstract + references|PDF
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Sensitivity to cerebral ischaemic insult in a rat model of stroke is determined by a single genetic locuspp364 - 367 Baxter Jeffs, James S. Clark, Niall H. Anderson, Julie Gratton, M. Julia Brosnan, Dominique Gauguier, John L. Reid, I. Mhairi Macrae
& Anna F. Dominiczak doi:10.1038/ng0897-364 Abstract + references|PDF
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Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mbpp368 - 371 Peter Gustavsson, Thiébaut-Noel Willig, Arie van Haeringen, Gil Tchernia, Irma Dianzani, Mikael Donnér, Göran Elinder, Jan-Inge Renter, Per-Gunnar Nilsson, Laurie Gordon, Gunnar Skeppner, Lisbeth van't Veer-Korthof, Anders Kreuger
& Niklas Dahl doi:10.1038/ng0897-368 Abstract + references|PDF
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Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrixpp372 - 374 Hermelita Winter, Mike A. Rogers, Lutz Langbein, Howard P. Stevens, Irene M. Leigh, Christine Labrèze, Sylvie Roul, Alain Taieb, Thomas Krieg
& Jürgen Schweizer doi:10.1038/ng0897-372 Abstract + references|PDF
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Somatic mutation of the MEN1 gene in parathyroid tumourspp375 - 378 Christina Heppner, Mary Beth Kester, Sunita K. Agarwal, Larisa V. Debelenko, Michael R. Emmert-Buck, Siradanahalli C. Guru, Pachiappan Manickam, Shodimu-Emmanuel Olufemi, Monica C. Skarulis, John L. Doppman, Richard H. Alexander, Young S. Kim, Suraj K. Saggar, Irina A. Lubensky, Zhengping Zhuang, Lance A. Liotta, Settara C. Chandrasekharappa, Francis S. Collins, Alien M. Spiegel, A. Lee Burns
& Stephen J. Marx doi:10.1038/ng0897-375 Abstract + references|PDF
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Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter genepp383 - 386 Mark D. Fleming, Cameron C. Trenor III, Maureen A. Su, Dorothee Foernzler, David R. Beier, William F. Dietrich
& Nancy C. Andrews doi:10.1038/ng0897-383 Abstract + references|PDF
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Sound-induced seizures in serotonin 5-HT2c receptor mutant micepp387 - 390 Thomas J. Brennan, William W. Seeley, Michael Kilgard, Christoph E. Schreiner
& Laurence H. Tecott doi:10.1038/ng0897-387 Abstract + references|PDF
(489K)
Mice lacking the vitamin D receptor exhibit impaired bone formation, uterine hypoplasia and growth retardation after weaningpp391 - 396 Tatsuya Yoshizawa, Yuki Handa, Yoshikatsu Uematsu, Shu Takeda, Keisuke Sekine, Yuko Yoshihara, Toru Kawakami, Kouki Arioka, Hiroshi Sato, Yasushi Uchiyama, Shoichi Masushige, Akiyoshi Fukamizu, Toshio Matsumoto
& Shigeaki Kato doi:10.1038/ng0897-391 Abstract + references|PDF
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atm and p53 cooperate in apoptosis and suppression of tumorigenesis, but not in resistance to acute radiation toxicitypp397 - 401 Christoph H. Westphal, Sheldon Rowan, Cornelius Schmaltz, Ari Elson, David E. Fisher
& Philip Leder doi:10.1038/ng0897-397 Abstract + references|PDF
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Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHPpp402 - 406 Todd R. Klesert, Anne D. Otten, Thomas D. Bird
& Stephen J. Tapscott doi:10.1038/ng0897-402 Abstract + references|PDF
(641K)
Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP genepp407 - 409 Charles A. Thornton, James P. Wymer, Zachary Simmons, Carolyn McClain
& Richard T. Moxley III doi:10.1038/ng0897-407 Abstract + references|PDF
(373K)
Corrigendum: Functional transplant of megabase human immunoglobulin loci recapitulates human antibody response in micep410 doi:10.1038/ng0897-410a PDF
(126K)
-synuclein—a link between Parkinson and Alzheimer diseases?
