Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 24

Results: 25

Identification of a microRNA signature associated with progression of leukoplakia to oral carcinoma.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4818, doi. 10.1093/hmg/ddp446

By:

Cervigne, Nilva K.;
Reis, Patricia P.;
Machado, Jerry;
Sadikovic, Bekim;
Bradley, Grace;
Galloni, Natalie Naranjo;
Pintilie, Melania;
Jurisica, Igor;
Perez-Ordonez, Bayardo;
Gilbert, Ralph;
Gullane, Patrick;
Irish, Jonathan;
Kamel-Reid, Suzanne

Publication type:

Article

NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4907, doi. 10.1093/hmg/ddp461

By:

Deveault, Catherine;
Qian, Jian Hua;
Chebaro, Wafaa;
Ao, Asangla;
Gilbert, Lucy;
Mehio, Amira;
Khan, Rabia;
Tan, Seang Lin;
Wischmeijer, Anita;
Coullin, Philippe;
Xie, Xing;
Slim, Rima

Publication type:

Article

Detecting natural selection by empirical comparison to random regions of the genome.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4853, doi. 10.1093/hmg/ddp457

By:

Yu, Fuli;
Keinan, Alon;
Chen, Hua;
Ferland, Russell J.;
Hill, Robert S.;
Mignault, Andre A.;
Walsh, Christopher A.;
Reich, David

Publication type:

Article

Contents Page.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 24, p. NP, doi. 10.1093/hmg/ddp491
Publication type:: Article

Adenosine deamination in human transcripts generates novel microRNA binding sites.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4801, doi. 10.1093/hmg/ddp443

By:

Borchert, Glen M.;
Gilmore, Brian L.;
Spengler, Ryan M.;
Xing, Yi;
Lanier, William;
Bhattacharya, Debashish;
Davidson, Beverly L.

Publication type:

Article

The mtDNA nt7778 G/T polymorphism affects autoimmune diseases and reproductive performance in the mouse.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4689, doi. 10.1093/hmg/ddp432

By:

Yu, Xinhua;
Wester-Rosenlöf, Lena;
Gimsa, Ulrike;
Holzhueter, Stephanie-Anna;
Marques, Andreia;
Jonas, Ludwig;
Hagenow, Kristin;
Kunz, Manfred;
Nizze, Horst;
Tiedge, Markus;
Holmdahl, Rikard;
Ibrahim, Saleh M.

Publication type:

Article

A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4756, doi. 10.1093/hmg/ddp438

By:

Pereira, Patricia Lopes;
Magnol, Laetitia;
Sahún, Ignasi;
Brault, Véronique;
Duchon, Arnaud;
Prandini, Paola;
Gruart, Agnès;
Bizot, Jean-Charles;
Chadefaux-Vekemans, Bernadette;
Deutsch, Samuel;
Trovero, Fabrice;
Delgado-García, José María;
Antonarakis, Stylianos E.;
Dierssen, Mara;
Herault, Yann

Publication type:

Article

EKV mutant connexin 31 associated cell death is mediated by ER stress.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4734, doi. 10.1093/hmg/ddp436

By:

Tattersall, Daniel;
Scott, Claire A.;
Gray, Colin;
Zicha, Daniel;
Kelsell, David P.

Publication type:

Article

Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4711, doi. 10.1093/hmg/ddp434

By:

Delous, Marion;
Hellman, Nathan E.;
Gaudé, Helori-Maël;
Silbermann, Flora;
Le Bivic, André;
Salomon, Rémi;
Antignac, Corinne;
Saunier, Sophie

Publication type:

Article

Selective neuronal requirement for huntingtin in the developing zebrafish.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4830, doi. 10.1093/hmg/ddp455

By:

Henshall, Tanya L.;
Tucker, Ben;
Lumsden, Amanda L.;
Nornes, Svanhild;
Lardelli, Michael T.;
Richards, Robert I.

Publication type:

Article

Editorial Board.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 24, p. NP, doi. 10.1093/hmg/ddp493
Publication type:: Article

Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4808, doi. 10.1093/hmg/ddp445

By:

Byun, Hyang-Min;
Siegmund, Kimberly D.;
Pan, Fei;
Weisenberger, Daniel J.;
Kanel, Gary;
Laird, Peter W.;
Yang, Allen S.

Publication type:

Article

Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4781, doi. 10.1093/hmg/ddp441

By:

Kishnani, Priya S.;
Chuang, Tzu-Po;
Bali, Deeksha;
Koeberl, Dwight;
Austin, Stephanie;
Weinstein, David A.;
Murphy, Elaine;
Chen, Ying-Ting;
Boyette, Keri;
Liu, Chu-Hao;
Chen, Yuan-Tsong;
Li, Ling-Hui

Publication type:

Article

Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4905, doi. 10.1093/hmg/ddp458

By:

Ashley, Neil;
O'Rourke, Anthony;
Smith, Conrad;
Adams, Susan;
Gowda, Vasantha;
Zeviani, Massimo;
Brown, Garry K.;
Fratter, Carl;
Poulton, Joanna

Publication type:

Article

Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4868, doi. 10.1093/hmg/ddp460

By:

Ferguson, Cole J.;
Lenk, Guy M.;
Meisler, Miriam H.

Publication type:

Article

Subscription Page.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 24, p. NP, doi. 10.1093/hmg/ddp494
Publication type:: Article

Preventing Ataxin-3 protein cleavage mitigates degeneration in a Drosophila model of SCA3.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4843, doi. 10.1093/hmg/ddp456

By:

Jung, Joonil;
Xu, Kexiang;
Lessing, Derek;
Bonini, Nancy M.

Publication type:

Article

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4879, doi. 10.1093/hmg/ddp444

By:

Moreno, Lina M.;
Mansilla, Maria Adela;
Bullard, Steve A.;
Cooper, Margaret E.;
Busch, Tamara D.;
Machida, Junichiro;
Johnson, Marla K.;
Brauer, David;
Krahn, Katherine;
Daack-Hirsch, Sandy;
L'Heureux, Jamie;
Valencia-Ramirez, Consuelo;
Rivera, Dora;
López, Ana Maria;
Moreno, Manuel A.;
Hing, Anne;
Lammer, Edward J.;
Jones, Marilyn;
Christensen, Kaare;
Lie, Rolv T.

Publication type:

Article

AIRE activated tissue specific genes have histone modifications associated with inactive chromatin.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4699, doi. 10.1093/hmg/ddp433

By:

Org, Tõnis;
Rebane, Ana;
Kisand, Kai;
Laan, Martti;
Haljasorg, Uku;
Andreson, Reidar;
Peterson, Pärt

Publication type:

Article

Impaired cone function and cone degeneration resulting from CNGB3 deficiency: down-regulation of CNGA3 biosynthesis as a potential mechanism.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4770, doi. 10.1093/hmg/ddp440

By:

Ding, Xi-Qin;
Harry, Cynthia S.;
Umino, Yumiko;
Matveev, Alexander V.;
Fliesler, Steven J.;
Barlow, Robert B.

Publication type:

Article

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4724, doi. 10.1093/hmg/ddp435

By:

Azzi, Salah;
Rossignol, Sylvie;
Steunou, Virginie;
Sas, Theo;
Thibaud, Nathalie;
Danton, Fabienne;
Le Jule, Maryline;
Heinrichs, Claudine;
Cabrol, Sylvie;
Gicquel, Christine;
Le Bouc, Yves;
Netchine, Irene

Publication type:

Article

Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders†.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4791, doi. 10.1093/hmg/ddp442

By:

Clark, Alice R.;
Sawyer, Gregory M.;
Robertson, Stephen P.;
Sutherland-Smith, Andrew J.

Publication type:

Article

Genetic association of FOXO1A and FOXO3A with longevity trait in Han Chinese populations.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4897, doi. 10.1093/hmg/ddp459

By:

Li, Yang;
Wang, Wen-Jing;
Cao, Huiqing;
Lu, Jiehua;
Wu, Chong;
Hu, Fang-Yuan;
Guo, Jian;
Zhao, Ling;
Yang, Fan;
Zhang, Yi-Xin;
Li, Wei;
Zheng, Gu-Yan;
Cui, Hanbin;
Chen, Xiaomin;
Zhu, Zhiming;
He, Hongbo;
Dong, Birong;
Mo, Xianming;
Zeng, Yi;
Tian, Xiao-Li

Publication type:

Article

Expression of the familial Mediterranean fever gene is regulated by nonsense-mediated decay†.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 24, p. 4746, doi. 10.1093/hmg/ddp437

By:

Grandemange, Sylvie;
Soler, Stephan;
Touitou, Isabelle

Publication type:

Article

Cover Page.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 24, p. NP, doi. 10.1093/hmg/ddp492
Publication type:: Article