Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 8

Results: 12

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1365, doi. 10.1093/hmg/ddl058

By:

Bell, Jordana Tzenova;
Wallace, Chris;
Dobson, Richard;
Wiltshire, Steven;
Mein, Charles;
Pembroke, Janine;
Brown, Morris;
Clayton, David;
Samani, Nilesh;
Dominiczak, Anna;
Webster, John;
Lathrop, G. Mark;
Connell, John;
Munroe, Patricia;
Caulfield, Mark;
Farrall, Martin

Publication type:

Article

Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1355, doi. 10.1093/hmg/ddl055

By:

Kock, Norman;
Naismith, Teresa V.;
Boston, Heather E.;
Ozelius, Laurie J.;
Corey, David P.;
Breakefield, Xandra O.;
Hanson, Phyllis I.

Publication type:

Article

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1343, doi. 10.1093/hmg/ddl054

By:

Zhu, Peng-Peng;
Soderblom, Cynthia;
Tao-Cheng, Jung-Hwa;
Stadler, Julia;
Blackstone, Craig

Publication type:

Article

Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1329, doi. 10.1093/hmg/ddl053

By:

Desai, Jayashree;
Shannon, Mark E.;
Johnson, Mahlon D.;
Ruff, David W.;
Hughes, Lori A.;
Kerley, Marilyn K.;
Carpenter, Donald A.;
Johnson, Dabney K.;
Rinchik, Eugene M.;
Culiat, Cymbeline T.

Publication type:

Article

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1319, doi. 10.1093/hmg/ddl052

By:

Merrill, Amy E.;
Bochukova, Elena G.;
Brugger, Sean M.;
Ishii, Mamoru;
Pilz, Daniela T.;
Wall, Steven A.;
Lyons, Karen M.;
Wilkie, Andrew O.M.;
Maxson, Robert E.

Publication type:

Article

Uneven size distribution of mammalian genes in the number of tissues expressed and in the number of co-expressed genes.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1313, doi. 10.1093/hmg/ddl051

By:

Liu, Song;
Zhang, Chi;
Zhou, Yaoqi

Publication type:

Article

Radiation-induced delayed cell death in a hypomorphic Artemis cell line.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1303, doi. 10.1093/hmg/ddl050

By:

Evans, Paul M.;
Woodbine, Lisa;
Riballo, Enriquetta;
Gennery, Andrew R.;
Hubank, Michael;
Jeggo, Penny A.

Publication type:

Article

Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapse.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1291, doi. 10.1093/hmg/ddl047

By:

Aartsen, Wendy M.;
Kantardzhieva, Albena;
Klooster, Jan;
van Rossum, Agnes G.S.H.;
van de Pavert, Serge A.;
Versteeg, Inge;
Cardozo, Bob Nunes;
Tonagel, Felix;
Beck, Susanne C.;
Tanimoto, Naoyuki;
Seeliger, Mathias W.;
Wijnholds, Jan

Publication type:

Article

Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in α-dystroglycanopathies.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1279, doi. 10.1093/hmg/ddl045

By:

Taniguchi, Mariko;
Kurahashi, Hiroki;
Noguchi, Satoru;
Fukudome, Takayasu;
Okinaga, Takeshi;
Tsukahara, Toshifumi;
Tajima, Youichi;
Ozono, Keiichi;
Nishino, Ichizo;
Nonaka, Ikuya;
Toda, Tatsushi

Publication type:

Article

Down-regulation of the cytoglobin gene, located on 17q25, in tylosis with oesophageal cancer (TOC): evidence for trans-allele repression.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1271, doi. 10.1093/hmg/ddl042

By:

McRonald, Fiona E.;
Liloglou, Triantafillos;
Xinarianos, George;
Hill, Laura;
Rowbottom, Lynn;
Langan, Joanne E.;
Ellis, Anthony;
Shaw, Joan M.;
Field, John K.;
Risk, Janet M.

Publication type:

Article

Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1259, doi. 10.1093/hmg/ddl041

By:

Monk, D.;
Sanches, R.;
Arnaud, P.;
Apostolidou, S.;
Hills, F.A.;
Abu-Amero, S.;
Murrell, A.;
Friess, H.;
Reik, W.;
Stanier, P.;
Constância, M.;
Moore, G.E.

Publication type:

Article

Expression of DISC1 binding partners is reduced in schizophrenia and associated with DISC1 SNPs.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1245, doi. 10.1093/hmg/ddl040

By:

Lipska, Barbara K.;
Peters, Tricia;
Hyde, Thomas M.;
Halim, Nader;
Horowitz, Cara;
Mitkus, Shruti;
Weickert, Cynthia Shannon;
Matsumoto, Mitsuyuki;
Sawa, Akira;
Straub, Richard E.;
Vakkalanka, Radhakrishna;
Herman, Mary M.;
Weinberger, Daniel R.;
Kleinman, Joel E.

Publication type:

Article