Letters in Nature Genetics (Englisch)
Nationallizenz
In:
Nature Genetics
;
10
, 2
;
124
;
1995
-
ISSN:
- Aufsatz (Zeitschrift) / Elektronische Ressource
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Titel:Letters in Nature Genetics
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Erschienen in:Nature Genetics ; 10, 2 ; 124
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Verlag:
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Erscheinungsdatum:01.06.1995
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Format / Umfang:1 pages
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ISSN:
-
DOI:
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Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
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Sprache:Englisch
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Datenquelle:
Inhaltsverzeichnis – Band 10, Ausgabe 2
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 123
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Predictions for polycystin| 1995
- 124
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Letters in Nature Genetics| 1995
- 125
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Chewing the fatKeightley, Peter D. et al. | 1995
- 126
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Atavisms and atavistic mutationsHall, Brian K. et al. | 1995
- 128
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What dwarfed Toulouse–Lautrec?Frey, Julia B. et al. | 1995
- 131
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Horizontal SINE transfer between vertebrate classesKordi\[sbreve], D. / Guben\[sbreve]ek, F. et al. | 1995
- 132
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Meiotic drive and myotonic dystrophyHurst, Gregory D.D. / Hurst, Laurence D. / Barrett, John A. et al. | 1995
- 133
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Reply to “Meiotic drive and myotonic dystrophy”Carey, Nessa / Johnson, Keith / Nokelainen, Pekka / Peltonen, Leena / Savontaus, Maria-Liisa / Juvonen, Vesa / Anvret, Maria / Grandell, Ulla / Chotai, Kokila / Robertson, Elaine et al. | 1995
- 135
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Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activityNaggert, Jürgen K. / Fricker, Lloyd D. / Varlamov, Oleg / Nishina, Patsy M. / Rouille, Yves / Steiner, Donald F. / Carroll, Raymond J. / Paigen, Beverly J. / Leiter, Edward H. et al. | 1995
- 143
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Ulcerative colitis and adenocarcinoma of the colon in Gαi2-deficient miceRudolph, Uwe / Finegold, Milton J. / Rich, Susan S. / Harriman, Gregory R. / Srinivasan, Yogambal / Brabet, Philippe / Boulay, Guylain / Bradley, Allan / Birnbaumer, Lutz et al. | 1995
- 151
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The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domainsHughes, Jim / Ward, Christopher J. / Peral, Belén / Aspinwall, Richard / Clark, Kevin / San Millán, José L. / Gamble, Vicki / Harris, Peter C. et al. | 1995
- 161
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Cytokine gene expression in epidermis with biological effects following injection of naked DNAHengge, Ulrich R. / Chan, Edward F. / Foster, Ruth A. / Walker, Patricia S. / Vogel, Jonathan C. et al. | 1995
- 167
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A novel gene, Translin, encodes a recombination hotspot binding protein associated with chromosomal translocationsAoki, Katsunori / Suzuki, Kenji / Sugano, Takashi / Tasaka, Tetsuya / Nakahara, Kazuhiko / Kuge, Osamu / Omori, Akira / Kasai, Masataka et al. | 1995
- 175
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A subset of p53-deficient embryos exhibit exencephalySah, Valerie P. / Attardi, Laura D. / Mulligan, George J. / Williams, Bart O. / Bronson, Roderick T. / Jacks, Tyler et al. | 1995
- 181
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A teratologic suppressor role for p53 in benzo(a)pyrene–treated transgenic p53-deficient miceNicol, Christopher J. / Harrison, Maureen L. / Laposa, Rebecca R. / Gimelshtein, Inga L. / Wells, Peter G. et al. | 1995
- 188
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p53 modulation of TFIIH–associated nucleotide excision repair activityWang, X.W. / Yeh, H. / Schaeffer, L. / Roy, R. / Moncollin, V. / Egly, J.-M. / Wang, Z. / Friedberg, E.C. / Evans, M.K. / Taffe, B.G. et al. | 1995
- 196
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Deregulation of both imprinted and expressed alleles of the insulin–like growth factor 2 gene during β–cell tumorigenesisChristofori, Gerhard / Naik, Paul / Hanahan, Douglas et al. | 1995
- 202
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Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24–q27.1Figuera, Luis E. / Pandolfo, Massimo / Dunne, Patrick W. / Cantú, Jose M. / Patel, Pragna I. et al. | 1995
- 208
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Rapid detection of BRCA1 mutations by the protein truncation testHogervorst, Frans B.L. / Cornelis, Renée S. / Bout, Mattie / Vliet, Margreethe van / Oosterwijk, Jan C. / Olmer, Renske / Bakker, Bert / Klijn, Jan G.M. / Vasen, Hans F.A. / Meijers-Heijboer, Hanna et al. | 1995
- 213
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Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coliKang, Seongman / Jaworski, Adam / Ohshima, Keiichi / Wells, Robert D. et al. | 1995
- 219
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Rapid evolution of a unique family of primate ribonuclease genesRosenberg, Helene F. / Dyer, Kimberly D. / Tiffany, H. Lee / Gonzalez, Monica et al. | 1995
- 224
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Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy–negative individualsTournamille, Christophe / Colin, Yves / Cartron, Jean Pierre / Le Van Kim, Caroline et al. | 1995
- 229
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Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresiaVidal, Frédérique / Aberdam, Daniel / Miquel, Corinne / Christiano, Angela M. / Pulkkinen, Leena / Uitto, Jouni / Ortonne, Jean-Paul / Meneguzzi, Guerrino et al. | 1995
- 235
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Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mappingGelb, Bruce D. / Edelson, Jacob G. / Desnick, Robert J. et al. | 1995
- 238
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The gene for pycnodysostosis maps to human chromosome 1cen–q21Polymeropoulos, Mihael H. / Ortiz De Luna, Rosa Isela / Ide, Susan E. / Torres, Rosarelis / Rubenstein, Jeffrey / Francomano, Clair A. et al. | 1995
- 240
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Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7Rowe, Rachel E. / Wapelhorst, Beth / Bell, Graeme I. / Risch, Neil / Spielman, Richard S. / Concannon, Patrick et al. | 1995
- 243
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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityPiccolo, F. / Roberds, S.L. / Jeanpierre, M. / Leturcq, F. / Azibi, K. / Beldjord, C. / Carrié, A. / Récan, D. / Chaouch, M. / Reghis, A. et al. | 1995
- 246
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Linkage of the gene for cystinosis to markers on the short arm of chromosome 17McDowell, Geraldine A. / Gahl, William A. / Stephenson, Leah A. / Schneider, Jerry A. / Weissenbach, Jean / Polymeropoulos, Mihael H. / Town, Margaret M. / van't Hoff, William / Farrall, Martin / Mathew, Christopher G. et al. | 1995
- 249
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Corrigendum: A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1| 1995
- 249
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Corrigendum: Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15| 1995
- 249
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Corrigendum: Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice| 1995