Works matching IS 09646906 AND DT 1996 AND VI 5 AND IP 8

Results: 17

Chromosomal Stabilisation by a Subtelomeric Rearrangement Involving Two Closely Related Alu Elements.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1163, doi. 10.1093/hmg/5.8.1163

By:

Flint, J.;
Rochette, J.;
Craddock, C. F.;
Dodé, C.;
Vignes, B.;
Horsley, S. W.;
Kearney, L.;
Buckle, V. J.;
Ayyub, H.;
Higgs, D. R.

Publication type:

Article

Differential Expression of Dystrophin Isoforms in Strains of mdx Mice with Different Mutations.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1149

By:

Im, Wha Bin;
Phelps, Stephanie F.;
Copen, Eecole H.;
Adams, Earl G.;
Slightom, Jerry L.;
Chamberlain, Jeffrey S.

Publication type:

Article

Mouse/Human Sequence Divergence in a Region with a Paternal-Specific Methylation Imprint at the Human H19 Locus.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1155, doi. 10.1093/hmg/5.8.1155

By:

Jinno, Yoshihiro;
Sengoku, Kazuo;
Nakao, Mitsuyoshi;
Tamate, Kenichi;
Miyamoto, Toshinobu;
Matsuzaka, Tetsuo;
Sutcliffe, James S.;
Anan, Tadashi;
Takuma, Naoyuki;
Nishiwaki, Kunihiko;
Ikeda, Yuichiro;
Ishimaru, Tadayuki;
Ishikawa, Mutsuo;
Niikawa, Norio

Publication type:

Article

Biallelic Expression of the IGF2 Gene in Human Breast Disease.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1123, doi. 10.1093/hmg/5.8.1123

By:

McCann, Amanda H.;
Miller, Nicola;
O'Meara, Anne;
Pedersen, Inge;
Keogh, Karina;
Gorey, Thomas;
Dervan, Peter A.

Publication type:

Article

The Kallmann Syndrome Gene Product Expressed in COS Cells is Cleaved on the Cell Surface to Yield a Diffusible Component.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1109, doi. 10.1093/hmg/5.8.1109

By:

Rugarli, Elena I.;
Ghezzi, Cristina;
Valsecchi, Valentina;
Ballabio, Andrea

Publication type:

Article

Human Usher 1B/Mouse shaker-1: The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor Cells.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1171, doi. 10.1093/hmg/5.8.1171

By:

El-Amraoui, Aziz;
Sahly, Iman;
Picaud, Serge;
Sahel, José;
Abitbol, Marc;
Petit, Christine

Publication type:

Article

The Fragile X Mental Retardation Protein is a Ribonucleoprotein Containing Both Nuclear Localization and Nuclear Export Signals.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1083, doi. 10.1093/hmg/5.8.1083

By:

Eberhart, Derek E.;
Malter, Henry E.;
Feng, Yue;
Warren, Stephen T.

Publication type:

Article

A Second Locus (GLC3B) for Primary Congenital Glaucoma (Buphthalmos) Maps to the 1p36 Region.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1199, doi. 10.1093/hmg/5.8.1199

By:

Akarsu, A. Nurten;
Turacli, M. Erol;
Aktan, S. Gulderen;
Barsoum-Homsy, Magda;
Chevrette, Line;
Sayli, B. Sitki;
Sarfarazi, Mansoor

Publication type:

Article

A Fine-Scale Comparison of the Human and Chimpanzee Genomes: Linkage, Linkage Disequilibrium and Sequence Analysis.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1131, doi. 10.1093/hmg/5.8.1131

By:

Crouau-Roy, B.;
Service, S.;
Slatkin, M.;
Freimer, N.

Publication type:

Article

Further Evidence for an Imprinted Gene for Neonatal Diabetes Localised to Chromosome 6q22–q23.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1117, doi. 10.1093/hmg/5.8.1117

By:

Temple, I. Karen;
Gardner, Rebecca J.;
Robinson, David O.;
Kibirige, Mohammed S.;
Ferguson, Arthur W.;
Baum, J. David;
Barber, John C. K.;
James, Rowena S.;
Shield, Julian P. H.

Publication type:

Article

Chromosome 11p15.5 Regional Imprinting: Comparative Analysis of KIP2 and H19 in Human Tissues and Wilms' Tumors.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1101, doi. 10.1093/hmg/5.8.1101

By:

Chung, Wai-Yee;
Yuan, Luwa;
Feng, Lin;
Hensle, Terrence;
Tycko, Benjamin

Publication type:

Article

Association between Atopic Asthma and a Coding Variant of FcεRIβ in a Japanese Population.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1129, doi. 10.1093/hmg/5.8.1129

By:

Shirakawa, T.;
Mao, X.-Q.;
Sasaki, S.;
Enomoto, T.;
Kawai, M.;
Morimoto, K.;
Hopkin, J.

Publication type:

Article

Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment (DFNA7) in a Large Norwegian Family.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1187, doi. 10.1093/hmg/5.8.1187

By:

Fagerheim, T.;
Nilssen, Ø.;
Raeymaekers, P.;
Brox, V.;
Moum, T.;
Elverland, H. H.;
Teig, E.;
Omland, H. H.;
Fostad, G. K.;
Tranebjærg, L.

Publication type:

Article

Identification of a Novel Sarcoglycan Gene at 5q33 Encoding a Sarcolemmal 35 kDa Glycoprotein.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1179, doi. 10.1093/hmg/5.8.1179

By:

Nigro, Vincenzo;
Piluso, Giulio;
Belsito, Angela;
Politano, Luisa;
Puca, Annibale Alessandro;
Papparella, Serenella;
Rossi, Elena;
Viglietto, Giuseppe;
Esposito, Maria Grazia;
Abbondanza, Ciro;
Medici, Nicola;
Molinari, Anna Maria;
Nigro, Giovanni;
Puca, Giovanni Alfredo

Publication type:

Article

Ott, a Mouse X-Linked Multigene Family Expressed Specifically During Meiosis.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1139, doi. 10.1093/hmg/5.8.1139

By:

Kerr, Shona M.;
Taggart, Mary H.;
Lee, Muriel;
Cooke, Howard J.

Publication type:

Article

A Ninth Locus (RP18) for Autosomal Dominant Retinitis Pigmentosa Maps in the Pericentromeric Region of Chromosome 1.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1193

By:

Ying Xu, Su;
Schwartz, Marianne;
Rosenberg, Thomas;
Gal, Andreas

Publication type:

Article

Subcellular Localization of the Huntington's Disease Gene Product in Cell Lines by Immunofluorescence and Biochemical Subcellular Fractionation.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1093, doi. 10.1093/hmg/5.8.1093

By:

De Rooij, Karien E.;
Dorsman, Josephine C.;
Smoor, Magda A.;
Den Dunnen, Johan T.;
Van Ommen, Gert-Jan B.

Publication type:

Article