Human Molecular Genetics - Table of Contents
Volume 07, January - December 1998: Issue 12
Location at: http://www.oup.co.uk/hmg/Volume_07/Issue_12/
Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes
Maki Wakamiya, Elizabeth A. Lindsay, Jaime A. Rivera-Perez, Antonio Baldini and Richard R. Behringer
Pages 1835-1840
Document ID = hmg_07_12_ddb231_gml
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Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development
Bruno Saint-Jore, Anne Puech, Jorg Heyer, Qingcong Lin, Cedric Raine, Raju Kucherlapati and Arthur I. Skoultchi
Pages 1841-1849
Document ID = hmg_07_12_ddb241_gml
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Multilocus linkage identifies two new loci for a Mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27
Holly D. Craig, Murat Gunel, Obed Cepeda, Eric W. Johnson, Louis Ptacek, Gary K. Steinberg, Christopher S. Ogilvy, Michael J. Berg, Stephen C. Crawford, R. Michael Scott, Elizabeth Steichen-Gersdorf, Ruth Sabroe, C. T. C. Kennedy, Gabrielle Mettler, M. Jill Beis, Alan Fryer, Issam A. Awad and Richard P. Lifton
Pages 1851-1858
Document ID = hmg_07_12_ddb230_gml
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Novel immunogenic antigen homologous to hyaluronidase in meningioma
Dirk Heckel, Nicole Comtesse, Nicole Brass, Nikolaus Blin, Klaus D. Zang and Eckart Meese
Pages 1859-1872
Document ID = hmg_07_12_ddb239_gml
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Analysis of the human GDNF gene reveals an inducible promoter, three exons, a triplet repeat within the 3[prime]-UTR and alternative splice products
Lena Grimm, Elke Holinski-Feder, Jens Teodoridis, Beatrix Scheffer, Dirk Schindelhauer, Thomas Meitinger and Marius Ueffing
Pages 1873-1886
Document ID = hmg_07_12_ddb235_gml
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Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene
M. J. Artiga, M. J. Bullido, A. Frank, I. Sastre, M. Recuero, M. A. Garcia, C. L. Lendon, S. W. Han, J. C. Morris, J. Vazquez, A. Goate and F. Valdivieso
Pages 1887-1892
Document ID = hmg_07_12_ddb233_gml
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Encapsidated adenovirus mini-chromosome-mediated delivery of genes to the retina: application to the rescue of photoreceptor degeneration
Rajendra Kumar-Singh and Debora B. Farber
Pages 1893-1900
Document ID = hmg_07_12_ddb232_gml
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Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia
Giuseppe De Michele, Francesca Cavalcanti, Chiara Criscuolo, Luigi Pianese, Antonella Monticelli, Alessandro Filla and Sergio Cocozza
Pages 1901-1906
Document ID = hmg_07_12_ddb238_gml
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Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases
Richard Houlston, Stephen Bevan, Andrew Williams, Joanne Young, Malcolm Dunlop, Paul Rozen, Charis Eng, David Markie, Kelly Woodford-Richens, Miguel A. Rodriguez-Bigas, Barbara Leggett, Kay Neale, Robin Phillips, Eamon Sheridan, Shirley Hodgson, Takeo Iwama, Diana Eccles, Walter Bodmer and Ian Tomlinson
Pages 1907-1912
Document ID = hmg_07_12_ddb236_gml
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Targeted replacement of normal and mutant CFTR sequences in human airway epithelial cells using DNA fragments
Kaarin K. Goncz, Karl Kunzelmann, Zhidong Xu and Dieter C. Gruenert
Pages 1913-1919
Document ID = hmg_07_12_ddb228_gml
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Molecular characterization of homozygous variegate porphyria
Andrew G. Roberts, Herve Puy, Tamara A. Dailey, Rhian R. Morgan, Sharon D. Whatley, Harry A. Dailey, Pavel Martasek, Yves Nordmann, Jean-Charles Deybach and George H. Elder
Pages 1921-1925
Document ID = hmg_07_12_ddb245_gml
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The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy
P. Burlet, C. Huber, S. Bertrandy, M. A. Ludosky, I. Zwaenepoel, O. Clermont, J. Roume, A. L. Delezoide, J. Cartaud, A. Munnich and S. Lefebvre
Pages 1927-1933
Document ID = hmg_07_12_ddb237_gml
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Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1
Chris Gunter, William Paradee, Dana C. Crawford, Kellen A. Meadows, James Newman, Catherine B. Kunst, David L. Nelson, Charles Schwartz, Anna Murray, James N. Macpherson, Stephanie L. Sherman and Stephen T. Warren
Pages 1935-1946
Document ID = hmg_07_12_ddb244_gml
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The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminus
Sara T. Winokur and Rita Shiang
Pages 1947-1952
Document ID = hmg_07_12_ddb229_gml
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Genetic association of an [alpha]2-macroglobulin (Val1000Ile) polymorphism and Alzheimer's disease
A. Liao, R. M. Nitsch, S. M. Greenberg, U. Finckh, D. Blacker, M. Albert, G. W. Rebeck, T. Gomez-Isla, A. Clatworthy, G. Binetti, C. Hock, T. Mueller-Thomsen, U. Mann, K. Zuchowski, U. Beisiegel, H. Staehelin, J. H. Growdon, R. E. Tanzi and B. T. Hyman
Pages 1953-1956
Document ID = hmg_07_12_ddb240_gml
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Localization of myotonic dystrophy protein kinase in human and rabbit tissues using a new panel of monoclonal antibodies
Y. C. N. Pham, Nguyen thi Man, Le Thanh Lam and G. E. Morris
Pages 1957-1965
Document ID = hmg_07_12_ddb234_gml
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Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome
Minoru S. H. Ko, Tracy A. Threat, Xueqian Wang, Joseph H. Horton, Yushun Cui, Xiaohong Wang, Eric Pryor, Jason Paris, Jeannine Wells-Smith, John R. Kitchen, Lucy B. Rowe, Janan Eppig, Toshihiko Satoh, Larry Brant, Hiroyuki Fujiwara, Shinichi Yotsumoto and Hiroshi Nakashima
Pages 1967-1978
Document ID = hmg_07_12_ddb243_gml
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Chromatin conformation of the H19 epigenetic mark
Amy T. Hark and Shirley M. Tilghman
Pages 1979-1985
Document ID = hmg_07_12_ddb242_gml
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Erratum
Pages 1987-1988
Document ID = hmg_07_12_erratum_gml
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