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| Editorial |  Top |
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Indian incense and sensibility pp111 - 112
doi:10.1038/ng0296-111
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(228K)
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| News and Views | Top |
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The malevolence of matchmaking pp113 - 114
Frederic G. Barr
doi:10.1038/ng0296-113
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(206K)
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Ain't misbehavin' - it's genetic! pp115 - 116
Timothy H. Moran, Roger H. Reeves, Derek Rogers
& Elizabeth Fisher
doi:10.1038/ng0296-115
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(221K)
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Touching base p116
doi:10.1038/ng0296-116
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(121K)
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A map to the future pp117 - 118
David R. Cox
& Richard M. Myers
doi:10.1038/ng0296-117
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(935K)
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| Obituary | Top |
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John Jacob Wasmuth (1946−1995) pp119 - 120
Nancy S. Wexler
doi:10.1038/ng0296-119
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(254K)
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| Correspondence | Top |
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Breaking laws and obeying rules p121
Jennifer A. Marshall Graves
doi:10.1038/ng0296-121a
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(137K)
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Reply to "Breaking laws and obeying rules" pp121 - 122
Andrea Ballabio
doi:10.1038/ng0296-121b
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(233K)
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Glucagon receptor gene mutation in essential hypertension p122
Susan M. Chambers
& Brian J. Morris
doi:10.1038/ng0296-122
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(112K)
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CNTF and endogenous psychoses? p123
Johannes Thome, Johannes Kornhuber, Alessandra Baumer, Michael Rösler, Helmut Beckmann
& Peter Riederer
doi:10.1038/ng0296-123
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(181K)
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| Progress | Top |
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What's in a face? pp124 - 129
Robin M. Winter
doi:10.1038/ng0296-124
Abstract + references | PDF
(607K)
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| Articles | Top |
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Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome pp130 - 136
The Treacher Collins Syndrome Collaborative Group, Jill Dixon, Sara J. Edwards, Amanda J. Gladwin, Michael J. Dixon, Stacie K. Loftus, Cynthia A. Bonner, Kathryn Koprivnikar
& John J. Wasmuth
doi:10.1038/ng0296-130
Abstract + references | PDF
(854K)
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Nf1 deficiency causes Ras-Dediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia pp137 - 143
David A. Largaespada, Camilynn I. Brannan, Nancy A. Jenkins
& Neal G. Copeland
doi:10.1038/ng0296-137
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(873K)
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Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells pp144 - 148
Gideon Bollag, D. Wade Clapp, Shane Shih, Felix Adler, You Yan Zhang, Patricia Thompson, Beverly J. Lange, Melvin H. Freedman, Frank McCormick, Tyler Jacks
& Kevin Shannon
doi:10.1038/ng0296-144
Abstract + references | PDF
(573K)
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Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias pp149 - 153
Takuro Nakamura, David A. Largaespada, John D. Shaughnessy Jr., Nancy A. Jenkins
& Neal G. Copeland
doi:10.1038/ng0296-149
Abstract + references | PDF
(526K)
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Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia pp154 - 158
Takuro Nakamura, David A. Largaespada, Maxwell P. Lee, Laura A. Johnson, Kazuma Ohyashiki, Keisuke Toyama, Sai Juan Chen, Cheryl L. Willman, I-Ming Chen, Andrew P Feinberg, Nancy A. Jenkins, Neal G. Copeland
& John D. Shaughnessy Jr.
doi:10.1038/ng0296-154
Abstract + references | PDF
(548K)
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The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9 pp159 - 167
Julian Borrow, Amanda M. Shearman, Vincent P. Stanton Jr., Reinhard Becher, Tucker Collins, Amy J. Williams, Ian Dubé, Fay Katz, Yok L. Kwong, Christine Morris, Kazuma Ohyashiki, Keisuke Toyama, Janet Rowley
& David E. Housman
doi:10.1038/ng0296-159
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(1,328K)
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Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency pp168 - 173
Baya Cherif-Zahar, Virginia Raynal, Pierre Gane, Marie-Geneviève Mattei, Pascal Bailly, Brian Gibbs, Yves Colin
& Jean-Pierre Cartron
doi:10.1038/ng0296-168
Abstract + references | PDF
(725K)
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Efficient modification of human chromosomal alleles using recombination-proficient chicken/human microcell hybrids pp174 - 182
Ellen S. Dieken, Elliot M. Epner, Steven Fiering, R. E. K. Fournier
& Mark Groudine
doi:10.1038/ng0296-174
Abstract + references | PDF
(1,025K)
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| Letters | Top |
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Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization pp183 - 185
Thomas Haaf, Giorgio Sirugo, Kenneth K. Kidd
& David C. Ward
doi:10.1038/ng0296-183
Abstract + references | PDF
(311K)
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Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein pp186 - 190
Yoshimi Kuroiwa, Tomoko Kaneko-Ishino, Fusako Kagitani, Takashi Kohda, Li-Lan Li, Masako Tada, Rika Suzuki, Minesuke Yokoyama, Toshihiko Shiroishi, Sigeharu Wakana, Sheila C. Barton, Fumitoshi Ishino
& M. Azim Surani
doi:10.1038/ng0296-186
Abstract + references | PDF
(619K)
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Brca1 deficiency results in early embryonic lethality characterized by neuroepithelial abnormalities pp191 - 194
Lori C. Gowen, B. Lee Johnson, Anne M. Latour, Kathleen K. Sulik
& Beverly H. Koller
doi:10.1038/ng0296-191
Abstract + references | PDF
(516K)
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Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria pp195 - 199
Raija L.P. Lindberg, Catherine Porcher, Bernard Grandchamp, Birgit Ledermann, Kurt Bürki, Sebastian Brandner, Adriano Aguzzi
& Urs A. Meyer
doi:10.1038/ng0296-195
Abstract + references | PDF
(659K)
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Differential regulation of telomerase activity and telomerase RNA during multi-stage tumorigenesis pp200 - 204
María A. Blasco, Michael Rizen, Carol W. Greider
& Douglas Hanahan
doi:10.1038/ng0296-200
Abstract + references | PDF
(914K)
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The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse pp205 - 208
Peri Tate, William Skarnes
& Adrian Bird
doi:10.1038/ng0296-205
Abstract + references | PDF
(549K)
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Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome pp209 - 211
Sumesh Sood, Zayz A. Eldadah, Wilma L. Krause, Iain Mclntosh
& Harry C. Dietz
doi:10.1038/ng0296-209
Abstract + references | PDF
(291K)
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Mutations in the founder of the MIP gene family underlie cataract development in the mouse pp212 - 215
Alan Shiels
& Steven Bassnett
doi:10.1038/ng0296-212
Abstract + references | PDF
(957K)
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Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption pp216 - 220
Martín G. Martín, Eric Turk, M. Pilar Lostao, Cynthia Kerner
& Ernest M. Wright
doi:10.1038/ng0296-216
Abstract + references | PDF
(526K)
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