Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 11

Results: 12

Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1359, doi. 10.1093/hmg/ddm086
By:
- Li, Zhongyou;
- Yu, Tao;
- Morishima, Masae;
- Pao, Annie;
- LaDuca, Jeffrey;
- Conroy, Jeffrey;
- Nowak, Norma;
- Matsui, Sei-Ichi;
- Shiraishi, Isao;
- Yu, Y. Eugene
Publication type:
Article
An integrative genomics strategy for systematic characterization of genetic loci modulating phenotypes.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1381, doi. 10.1093/hmg/ddm089
By:
- Bao, Lei;
- Peirce, Jeremy L.;
- Zhou, Mi;
- Li, Hongqiang;
- Goldowitz, Dan;
- Williams, Robert W.;
- Lu, Lu;
- Cui, Yan
Publication type:
Article
Epigenetic defects of hepatocellular carcinoma are already found in non-neoplastic liver cells from patients with hereditary haemochromatosis.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1335, doi. 10.1093/hmg/ddm082
By:
- Lehmann, Ulrich;
- Wingen, Luzie U.;
- Brakensiek, Kai;
- Wedemeyer, Heiner;
- Becker, Thomas;
- Heim, Albert;
- Metzig, Kathleen;
- Hasemeier, Britta;
- Kreipe, Hans;
- Flemming, Peer
Publication type:
Article
Degenerative phenotypes caused by the combined deficiency of murine HIP1 and HIP1r are rescued by human HIP1.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1279, doi. 10.1093/hmg/ddm076
By:
- Bradley, Sarah V.;
- Hyun, Teresa S.;
- Oravecz-Wilson, Katherine I.;
- Li, Lina;
- Waldorff, Erik I.;
- Ermilov, Alexander N.;
- Goldstein, Steven A.;
- Zhang, Claire X.;
- Drubin, David G.;
- Varela, Kate;
- Parlow, Al;
- Dlugosz, Andrzej A.;
- Ross, Theodora S.
Publication type:
Article
Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1343, doi. 10.1093/hmg/ddm084
By:
- Meirhaeghe, Aline;
- Sandhu, Manjinder S.;
- McCarthy, Mark I.;
- de Groote, Pascal;
- Cottel, Dominique;
- Arveiler, Dominique;
- Ferrières, Jean;
- Groves, Christopher J.;
- Hattersley, Andrew T.;
- Hitman, Graham A.;
- Walker, Mark;
- Wareham, Nicholas J.;
- Amouyel, Philippe
Publication type:
Article
Apoptotic mechanisms in mutant LRRK2-mediated cell death.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1319, doi. 10.1093/hmg/ddm080
By:
- Iaccarino, Ciro;
- Crosio, Claudia;
- Vitale, Carmine;
- Sanna, Giovanna;
- Carrì, Maria Teresa;
- Barone, Paolo
Publication type:
Article
The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1351, doi. 10.1093/hmg/ddm085
By:
- Löwe, Thomas;
- Kley, Rudolf A.;
- van der Ven, Peter F.M.;
- Himmel, Mirko;
- Huebner, Angela;
- Vorgerd, Matthias;
- Fürst, Dieter O.
Publication type:
Article
Genomewide suggestive linkage of opioid dependence to chromosome 14q.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1327, doi. 10.1093/hmg/ddm081
By:
- Lachman, Herbert M.;
- Fann, Cathy S.J.;
- Bartzis, Michael;
- Evgrafov, Oleg V.;
- Rosenthal, Richard N.;
- Nunes, Edward V.;
- Miner, Christian;
- Santana, Maria;
- Gaffney, Jebediah;
- Riddick, Amy;
- Hsu, Chia-Lin;
- Knowles, James A.
Publication type:
Article
Histones associated with downregulated genes are hypo-acetylated in Huntington's disease models.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1293, doi. 10.1093/hmg/ddm078
By:
- Sadri-Vakili, Ghazaleh;
- Bouzou, Bérengère;
- Benn, Caroline L.;
- Kim, Mee-Ohk;
- Chawla, Prianka;
- Overland, Ryan P.;
- Glajch, Kelly E.;
- Xia, Eva;
- Qiu, Zhihua;
- Hersch, Steven M.;
- Clark, Timothy W.;
- Yohrling, George J.;
- Cha, Jang-Ho J.
Publication type:
Article
Signatures of recent positive selection at the ATP-binding cassette drug transporter superfamily gene loci.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1367, doi. 10.1093/hmg/ddm087
By:
- Wang, Zihua;
- Wang, Jingbo;
- Tantoso, Erwin;
- Wang, Baoshuang;
- Tai, Amy Y.P.;
- Ooi, London L.P.J.;
- Chong, Samuel S.;
- Lee, Caroline G.L.
Publication type:
Article
Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1307, doi. 10.1093/hmg/ddm079
By:
- Davies, Vanessa J.;
- Hollins, Andrew J.;
- Piechota, Malgorzata J.;
- Yip, Wanfen;
- Davies, Jennifer R.;
- White, Kathryn E.;
- Nicols, Phillip P.;
- Boulton, Michael E.;
- Votruba, Marcela
Publication type:
Article
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1271
By:
- Camp, Nicola J.;
- Cannon-Albright, Lisa A.;
- Farnham, James M.;
- Baffoe-Bonnie, Agnes B.;
- George, Asha;
- Powell, Isaac;
- Bailey-Wilson, Joan E.;
- Carpten, John D.;
- Giles, Graham G.;
- Hopper, John L.;
- Severi, Gianluca;
- English, Dallas R.;
- Foulkes, William D.;
- Maehle, Lovise;
- Moller, Pal;
- Eeles, Ros;
- Easton, Douglas;
- Badzioch, Michael D.;
- Whittemore, Alice S.;
- Oakley-Girvan, Ingrid
Publication type:
Article