Hair hear! (Englisch)
- Neue Suche nach: Phimister, B.
- Neue Suche nach: Phimister, B.
In:
NATURE GENETICS
;
19
, 1
;
8
;
1998
-
ISSN:
- Aufsatz (Zeitschrift) / Print
-
Titel:Hair hear!
-
Beteiligte:Phimister, B. ( Autor:in )
-
Erschienen in:NATURE GENETICS ; 19, 1 ; 8
-
Verlag:
- Neue Suche nach: NATURE PUBLISHING CO.
-
Erscheinungsdatum:01.01.1998
-
Format / Umfang:8 pages
-
ISSN:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Print
-
Sprache:Englisch
- Neue Suche nach: 576.5
- Weitere Informationen zu Dewey Decimal Classification
-
Klassifikation:
DDC: 576.5 -
Datenquelle:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Inhaltsverzeichnis – Band 19, Ausgabe 1
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.
- 1
-
HUGO—a midlife crisis?| 1998
- 3
-
The lupus paradoxCarroll, Michael C. et al. | 1998
- 4
-
The genomics of a hot-water makerKlenk, Hans-Peter et al. | 1998
- 6
-
Dyskeratosis and ribosomal rebellionLuzzatto, Lucio / Karadimitris, Anastasios et al. | 1998
- 8
-
Hair hear!Phimister, Bette et al. | 1998
- 9
-
Sibling rivalry, arrested development and chromosomal mayhemFriend, Stephen H. / Tapscott, Stephen J. et al. | 1998
- 10
-
The politics of germline therapyBonnicksen, Andrea L. et al. | 1998
- 12
-
Touching base| 1998
- 13
-
The kinetics of rAAV integration in the liverMiao, Carol H. / Snyder, Richard O. / Schowalter, David B. / Patijn, Gijsbert A. / Donahue, Brian / Winther, Brian / Kay, Mark A. et al. | 1998
- 15
-
An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcriptRougeulle, Claire / Cardoso, Carlos / Fontés, Michel / Colleaux, Laurence / Lalande, Marc et al. | 1998
- 17
-
HNPCC associated with germline mutation in the TGF-β type II receptor geneLu, Shi-Long / Kawabata, Masahiro / Imamura, Takeshi / Akiyama, Yoshimitsu / Nomizu, Tadashi / Miyazono, Kohei / Yuasa, Yasuhito et al. | 1998
- 19
-
The impact of L1 retrotransposons on the human genomeKazazian, Haig H. / Moran, John V. et al. | 1998
- 25
-
A mouse model for Prader-Willi syndrome imprinting-centre mutationsYang, Tao / Adamson, Todd E. / Resnick, James L. / Leff, Stuart / Wevrick, Rachel / Francke, Uta / Jenkins, Nancy A. / Copeland, Neal G. / Brannan, Camilynn I. et al. | 1998
- 32
-
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functionsHeiss, Nina S. / Knight, Stuart W. / Vulliamy, Tom J. / Klauck, Sabine M. / Wiemann, Stefan / Mason, Philip J. / Poustka, Annemarie / Dokal, Inderjeet et al. | 1998
- 39
-
Duplication of ATR inhibits MyoD, induces aneuploidy and eliminates radiation-induced G1 arrestSmith, Leslie / Liu, Shu Jing / Goodrich, Lisa / Jacobson, David / Degnin, Catherine / Bentley, Nicole / Carr, Antony / Flaggs, Gail / Keegan, Kathleen / Hoekstra, Merl et al. | 1998
- 47
-
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndromeDreyer, Sandra D. / Zhou, Guang / Baldini, Antonio / Winterpacht, Andreas / Zabel, Bernhard / Cole, William / Johnson, Randy L. / Lee, Brendan et al. | 1998
- 51
-
Limb and kidney defects in Lmx1b mutant mice suggest an involvement of Imx1B in human nail pafella syndromeChen, H. / Lun, Y. / Ovchinnikov, D. / Kokubo, H. / Oberg, K. C. / Pepicelli, C. V. / Gan, L. / Lee, B. / Johnson, R. L. et al. | 1998
- 51
-
Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndromeChen, Haixu / Lun, Yi / Ovchinnikov, Dmitry / Kokubo, Hiroki / Oberg, Kerby C. / Pepicelli, Carmen V. / Can, Lin / Lee, Brendan / Johnson, Randy L. et al. | 1998
- 56
-
Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodiesBotto, Marina / Dell' Agnola, Chiara / Bygrave, Anne E. / Thompson, E. Mary / Cook, H. Terence / Petry, Franz / Loos, Michael / Pandolfi, Pier Paolo / Walport, Mark J. et al. | 1998
- 60
-
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairmentVerhoeven, Kristien / Laer, Lut Van / Kirschhofer, Karin / Legan, P. Kevin / Hughes, David C. / Schatteman, Isabelle / Verstreken, Margriet / Hauwe, Peter Van / Coucke, Paul / Chen, Achih et al. | 1998
- 63
-
SMN oligomerization defect correlates with spinal muscular atrophy severityLorson, Christian L. / Strasswimmer, John / Yao, Jun-Mei / Baleja, James D. / Hahnen, Eric / Wirth, Brunhilde / Le, Thanh / Burghes, Arthur H.M. / Androphy, Elliot J. et al. | 1998
- 67
-
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)Belin, Valérie / Cusin, Veronica / Viot, Géraldine / Girlich, Delphine / Toutain, Annick / Moncla, Anne / Vekemans, Michel / Merrer, Martine Le / Munnich, Arnold / Cormier-Daire, Valérie et al. | 1998
- 70
-
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosisShears, Deborah J. / Vassal, Humberto J. / Goodman, Frances R. / Palmer, Rodger W. / Reardon, William / Superti-Furga, Andrea / Scambler, Peter J. / Winter, Robin M. et al. | 1998
- 74
-
Human deltex is a conserved regulator of Notch signallingMatsuno, Kenji / Eastman, Deborah / Mitsiades, Tim / Quinn, Anne Marie / Carcanciu, Maria Louisa / Ordentlich, Peter / Kadesch, Tom / Artavanis-Tsakonas, Spyros et al. | 1998
- 79
-
Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient miceRafael, Jill A. / Tinsley, Jonathon M. / Potter, Allyson C. / Deconinck, Anne E. / Davies, Kay E. et al. | 1998
- 83
-
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesisMacchia, Paolo Emidio / Lapi, Paola / Krude, Heiko / Pirro, Maria Teresa / Missero, Caterina / Chiovato, Luca / Souabni, Abdallah / Baserga, Mariangiola / Tassi, Vittorio / Pinchera, Aldo et al. | 1998
- 87
-
Follicular cells of the thyroid gland require Pax8 gene functionMansouri, Ahmed / Chowdhury, Kamal / Gruss, Peter et al. | 1998
- 91
-
Correction of disease-causing CBS mutations in yeastShan, Xiaoyin / Kruger, Warren D. et al. | 1998
- 94
-
Mutations in the integrin α7 gene cause congenital myopathyHayashi, Yukiko K. / Chou, Fan-Li / Engvall, Eva / Ogawa, Megumu / Matsuda, Chie / Hirabayashi, Shinichi / Yokochi, Kenji / Ziober, Barry L. / Kramer, Randall H. / Kaufman, Stephen J. et al. | 1998
- 98
-
Association of the INS VNTR with size at birthDunger, David B. / Ong, Ken K.L. / Huxtable, Stewart J. / Sherriff, Andrea / Woods, Kathryn A. / Ahmed, Marion L. / Golding, Jean / Pembrey, Marcus E. / Ring, Sue / Bennett, Simon T. et al. | 1998
- 102
-
Growth retardation and tumour inhibition by BRCA1| 1998
- 102
-
Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome| 1998
- 102
-
Distribution of olfactory receptor genes in the human genome| 1998