Works matching IS 09646906 AND DT 1999 AND VI 8 AND IP 4

Results: 20

Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epithelium.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 575, doi. 10.1093/hmg/8.4.575

By:

Chang, Jinghua T.;
Esumi, Noriko;
Moore, Kathryn;
Li, Yuanyuan;
Zhang, Suiyuan;
Chew, Christina;
Goodman, Barbara;
Rattner, Amir;
Moody, Sally;
Stetten, Gail;
Campochiaro, Peter A.;
Zack, Donald J.

Publication type:

Article

A genome-wide screen for asthma-associated quantitative trait loci in a mouse model of allergic asthma.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 601, doi. 10.1093/hmg/8.4.601

By:

Zhang, Youming;
Lefort, Jean;
Kearsey, Virginia;
Lapa e Silva, José Roberto;
Cookson, William O. C. M.;
Vargaftig, B. Boris

Publication type:

Article

Characterization of dystrophin and utrophin diversity in the mouse.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 593, doi. 10.1093/hmg/8.4.593

By:

Lumeng, Carey N.;
Phelps, Stephanie F.;
Rafael, Jill A.;
Cox, Greg A.;
Hutchinson, Tressia L.;
Begy, Catherine R.;
Adkins, Erika;
Wiltshire, Rodney;
Chamberlain, Jeffrey S.

Publication type:

Article

In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 555, doi. 10.1093/hmg/8.4.555

By:

Schweizer, Johannes;
Zynger, Debra;
Francke, Uta

Publication type:

Article

Bex1, a gene with increased expression in parthenogenetic embryos, is a member of a novel gene family on the mouse X chromosome.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 611, doi. 10.1093/hmg/8.4.611

By:

Brown, Anna L.;
Kay, Graham F.

Publication type:

Article

Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 607, doi. 10.1093/hmg/8.4.607

By:

Richards, Frances M.;
McKee, Shane A.;
Rajpar, M. Helen;
Cole, Trevor R. P.;
Evans, D. Gareth R.;
Jankowski, Janusz A.;
McKeown, Carole;
Sanders, D. Scott A.;
Maher, Eamonn R.

Publication type:

Article

Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 621, doi. 10.1093/hmg/8.4.621

By:

Deckert, Jürgen;
Catalano, Marco;
Syagailo, Yana V.;
Bosi, Monica;
Okladnova, Olga;
Di Bella, Daniela;
Nöthen, Markus M.;
Maffei, Piermario;
Franke, Petra;
Fritze, Jürgen;
Maier, Wolfgang;
Propping, Peter;
Beckmann, Helmut;
Bellodi, Laura;
Lesch, Klaus-Peter

Publication type:

Article

Genome-wide screen for systemic lupus erythematosus susceptibility genes in multiplex families.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 639, doi. 10.1093/hmg/8.4.639

By:

Shai, Ruty;
Quismorio Jr, Francisco P.;
Li, Lily;
Kwon, Oh-Joong;
Morrison, John;
Wallace, Daniel J.;
Neuwelt, C. Michael;
Brautbar, Chaim;
Gauderman, W. James;
Jacob, Chaim O.

Publication type:

Article

Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 655, doi. 10.1093/hmg/8.4.655

By:

Tang, Nelson L. S.;
Ganapathy, V.;
Wu, Xiang;
Hui, Joannie;
Seth, Pankaj;
Yuen, Patrick M. P.;
Fok, T. F.;
Hjelm, N. M.

Publication type:

Article

Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 673, doi. 10.1093/hmg/8.4.673

By:

Chai, Yaohui;
Koppenhafer, Stacia L.;
Shoesmith, Sarah J.;
Perez, Matthew K.;
Paulson, Henry L.

Publication type:

Article

Structural and functional characterization of the mouse promoter: implications for campomelic dysplasia.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 691, doi. 10.1093/hmg/8.4.691

By:

Kanai, Yoshiakira;
Koopman, Peter

Publication type:

Article

Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (/) arise from a winged helix/forkhead transcriptionfactor gene.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 625, doi. 10.1093/hmg/8.4.625

By:

Hong, Hee-Kyung;
Lass, Jonathan H.;
Chakravarti, Aravinda

Publication type:

Article

MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic endometrial cancers.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 661, doi. 10.1093/hmg/8.4.661

By:

Simpkins, Sally B.;
Bocker, Tina;
Swisher, Elizabeth M.;
Mutch, David G.;
Gersell, Deborah J.;
Kovatich, Albert J.;
Palazzo, Juan P.;
Fishel, Richard;
Goodfellow, Paul J.

Publication type:

Article

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 683, doi. 10.1093/hmg/8.4.683

By:

Lee, Maxwell P.;
Brandenburg, Sheri;
Landes, Gregory M.;
Adams, Mark;
Miller, Glenn;
Feinberg, Andrew P.

Publication type:

Article

Inner ear and kidney anomalies caused by IAP insertion in an intron of the gene in a mouse model of BOR syndrome.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 645, doi. 10.1093/hmg/8.4.645

By:

Johnson, Kenneth R.;
Cook, Susan A.;
Erway, Lawrence C.;
Matthews, Angela N.;
Sanford, L. Phillip;
Paradies, Nancy E.;
Friedman, Rick A.

Publication type:

Article

Genetic mapping of a maternal locus responsible for familial hydatidiform moles.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 667, doi. 10.1093/hmg/8.4.667

By:

Bou Moglabey, Yolla;
Kircheisen, Renate;
Seoud, Muhieddine;
El Mogharbel, Nisrine;
Van den Veyver, Ignatia;
Slim, Rima

Publication type:

Article

Functional domains of the SYT and SYT-SSX synovial sarcoma translocation proteins and co-localization with the SNF protein BRM in the nucleus.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 585, doi. 10.1093/hmg/8.4.585

By:

Thaete, C.;
Brett, D.;
Monaghan, P.;
Whitehouse, S.;
Rennie, G.;
Rayner, E.;
Cooper, C. S.;
Goodwin, G.

Publication type:

Article

A wide variety of mutations in the gene are responsible for autosomal recessive parkinsonism in Europe.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 567

By:

Abbas, Nacer;
Lücking, Christoph B.;
Ricard, Sylvain;
Dürr, Alexandra;
Bonifati, Vincenzo;
De Michele, Giuseppe;
Bouley, Sandrine;
Vaughan, Jenny R.;
Gasser, Thomas;
Marconi, Roberto;
Broussolle, Emmanuel;
Brefel-Courbon, Christine;
Harhangi, Biswadjiet S.;
Oostra, Ben A.;
Fabrizio, Edito;
Böhme, Georg A.;
Pradier, Laurent;
Wood, Nick W.;
Filla, Alessandro;
Meco, Giuseppe

Publication type:

Article

Isolation and embryonic expression of the novel mouse gene , the homologue of , a candidate gene for the Miller-Dieker syndrome.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 697, doi. 10.1093/hmg/8.4.697

By:

Grimm, Christina;
Spörle, Ralf;
Schmid, Thomas E.;
Adler, Ilse-Dore;
Adamski, Jerzy;
Schughart, Klaus;
Graw, Jochen

Publication type:

Article

Association of an extended haplotype in the gene with progressive supranuclear palsy.

Published in:

Human Molecular Genetics, 1999, v. 8, n. 4, p. 711, doi. 10.1093/hmg/8.4.711

By:

Baker, Matt;
Litvan, Irene;
Houlden, Henry;
Adamson, Jennifer;
Dickson, Dennis;
Perez-Tur, Jordi;
Hardy, John;
Lynch, Timothy;
Bigio, Eileen;
Hutton, Mike

Publication type:

Article