Reliability of DNA-based sex testsp103 Fabrício R. Santos, Arpita Pandya
& Chris Tyler-Smith doi:10.1038/ng0298-103 References|PDF
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Ptch2, a second mouse Patched gene is co-expressed with Sonic hedgehogpp104 - 106 Jun Motoyama, Takashi Takabatake, Kazuhito Takeshima
& Chi-chung Hui doi:10.1038/ng0298-104 References|PDF
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AlaSOPro mutation in the gene encoding -synuclein in Parkinson's diseasepp106 - 108 Rejko Krüger, Wilfried Kuhn, Thomas Müller, Dirk Woitalla, Manuel Graeber, Sigfried Kösel, Horst Przuntek, Jörg T. Epplen, Ludger Schols
& Olaf Riess doi:10.1038/ng0298-106 References|PDF
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Supersonic congenics?p108 Richard Behringer doi:10.1038/ng0298-108 References|PDF
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Mitochondrial mutation rate revisited: hot spots and polymorphismpp109 - 110 Elena Jazin, Himla Soodyall, Paula Jalonen, Eva Lindholm, Mark Stoneking
& Ulf Gyllensten doi:10.1038/ng0298-109 References|PDF
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Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretchpp111 - 117 Shuichi Igarashi, Reiji Koide, Takayoshi Shimohata, Mitsunori Yamada, Yasuko Hayashi, Hiroki Takano, Hidetoshi Date, Mutsuo Oyake, Toshiya Sato, Aki Sato, Shigekimi Egawa, Takeshi Ikeuchi, Hajime Tanaka, Ryoichi Nakano, Keiko Tanaka, Isao Hozumi, Takashi Inuzuka, Hitoshi Takahashi
& Shoji Tsuji doi:10.1038/ng0298-111 Abstract + references|PDF
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Mice with gene targetted prion protein alterations show that Prnp, Sine and Prni are congruentpp118 - 125 Richard C. Moore, James Hope, Patricia A. McBride, Irene McConnell, James Selfridge, David W. Melton
& Jean C. Manson doi:10.1038/ng0298-118 Abstract + references|PDF
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Distinct interactions of PML-RAR and PLZF-RAR with co-repressors determine differential responses to RA in APLpp126 - 135 Li-Zhen He, Fabien Guidez, Carla Tribioli, Daniela Peruzzi, Martin Ruthardt, Arthur Zelent
& Pier Paolo Pandolfi doi:10.1038/ng0298-126 Abstract + references|PDF
(1,271K)
An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombinationpp136 - 141 Erik N. Meyers, Mark Lewandoski1
& Gail R. Martin doi:10.1038/ng0298-136 Abstract + references|PDF
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The itchy locus encodes a novel ubiquitin protein ligase that is disrupted in a18H micepp143 - 146 William L. Perry, Carolyn M. Hustad, Debra A. Swing, T. Norene O'Sullivan, Nancy A. Jenkins
& Neal G. Copeland doi:10.1038/ng0298-143 Abstract + references|PDF
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Mutations in PROP1 cause familial combined pituitary hormone deficiencypp147 - 149 Wei Wu, Joy D. Cogan, Roland W. Pfäffle, Jeremy S. Dasen, Herwig Frisch, Shawn M. O'Connell1, Sarah E. Flynn, Milton R. Brown, Primus E. Mullis, John S. Parks, John A. Phillips III
& Michael G. Rosenfeld doi:10.1038/ng0298-147 Abstract + references|PDF
(441K)
Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregatespp150 - 154 Diane Martindale, Abigail Hackam, Andrew Wieczorek, Lisa Ellerby, Cheryl Wellington, Krista McCutcheon, Roshni Singaraja, Parsa Kazemi-Esfarjani, Richard Devon, Seung U. Kim, Dale E. Bredesen, Frank Tufaro
& Michael R. Hayden doi:10.1038/ng0298-150 Abstract + references|PDF
(832K)
Evolutionary sequence comparisons using high-density oligonucleotide arrayspp155 - 158 Joseph G. Hacia, Wojciech Makalowski, Keith Edgemon, Michael R. Erdos, Christiane M. Robbins, Stephen P. A. Fodor, Lawrence C. Brody
& Francis S. Collins doi:10.1038/ng0298-155 Abstract + references|PDF
(800K)
A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutasepp159 - 163 Simon Melov, Julie A. Schneider, Brian J. Day, Douglas Hinerfeld, Pinar Coskun, Suzanne S. Mirra, James D. Crapo
& Douglas C. Wallace doi:10.1038/ng0298-159 Abstract + references|PDF
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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophypp164 - 167 Bernard Brais, Jean-Pierre Bouchard, Ya-Gang Xie, Daniel L. Rochefort, Nathalie Chrétien, Fernando M.S. Tomé, Ronald G. Lafrentére, Johanna M. Rommens, Eichiro Uyama, Osamu Nohira, Segiu Blumen, Amos D. Korcyn, Peter Heutink, Jean Mathieu, André Duranceau, Francois Codère, Michel Fardeau
& Guy A. Rouleau doi:10.1038/ng0298-164 Abstract + references|PDF
(493K)
Localisation of a gene implicated in a severe speech and language disorderpp168 - 170 Simon E. Fisher, Faraneh Vargha-Khadem, Kate E. Watkins, Anthony P. Monaco
& Marcus E. Pembrey doi:10.1038/ng0298-168 Abstract + references|PDF
(365K)
SOX10 mutations in patients with Waardenburg-Hirschsprung diseasepp171 - 173 Véronique Pingault, Nadège Bondurand, Kirsten Kuhlbrodt, Derk E. Goerich, Marie-Odette Préhu, Aldamaria Puliti, Beate Herbarth, Irm Hermans-Borgmeyer, Eric Legius, Gert Matthijs, Jeanne Amiel, Stanislas Lyonnet, Isabella Ceccherini, Giovanni Romeo, Jill Clayton Smith, Andrew P. Read, Michael Wegner
& Michel Goossens doi:10.1038/ng0298-171 Abstract + references|PDF
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Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosapp174 - 176 Stephanie A. Hagstrom, Michael A. North, Patsy M. Nishina, Eliot L. Berson
& Thaddeus P. Dryja doi:10.1038/ng0298-174 Abstract + references|PDF
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TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosapp177 - 179 Poulabi Banerjee, Patrick W. Kleyn, James A. Knowles, Charles A. Lewis, Barbara M. Ross, Enrico Parano, Steve G. Kovats, John J. Lee, Graciela K. Penchaszadeh, Jürg Ott, Samuel G. Jacobson
& T. Conrad Gilliam doi:10.1038/ng0298-177 Abstract + references|PDF
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Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicitypp180 - 183 Gudrun Schiedner, Núria Morral, Robin J. Parks, Ying Wu, Suzanne C. Koopmans, Claire Langston, Frank L. Graham, Arthur L. Beaudet
& Stefan Kochanek doi:10.1038/ng0298-180 Abstract + references|PDF
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A novel ETV6-NTRK3 gene fusion in congenital fibrosarcomapp184 - 187 Stevan R. Knezevich, Deborah E. McFadden, Wen Tao, Jerian F. Lim
& Poul H.B. Sorensen doi:10.1038/ng0298-184 Abstract + references|PDF
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GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrierpp188 - 191 Glen Seidner, Marcela Garcia Alvarez, Jih-I Yeh, Kevin R. O'Driscoll, Jörg Klepper, Tammy S. Stump, Dong Wang, Nancy B. Spinner, Morris J. Birnbaum
& Darryl C. De Vivo doi:10.1038/ng0298-188 Abstract + references|PDF
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Mutation detection and typing of polymorphic loci through double-strand conformation analysispp192 - 194 J. Rafael Argüello, Ann-Margaret Little, Andrea L. Pay, David Gallardo, Isabel Rojas, Steven G.E. Marsh, John M. Goldman
& J. Alejandro Madrigal doi:10.1038/ng0298-192 Abstract + references|PDF
(369K)
-synuclein in Parkinson's disease
