Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 19

Results: 15

A set of differentially expressed miRNAs, including miR-30a-5p, act as post-transcriptional inhibitors of BDNF in prefrontal cortex.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3030, doi. 10.1093/hmg/ddn201

By:

Mellios, Nikolaos;
Huang, Hsien-Sung;
Grigorenko, Anastasia;
Rogaev, Evgeny;
Akbarian, Schahram

Publication type:

Article

First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2967, doi. 10.1093/hmg/ddn195

By:

Kapeller, Johannes;
Houghton, Lesley A.;
Mönnikes, Hubert;
Walstab, Jutta;
Möller, Dorothee;
Bönisch, Heinz;
Burwinkel, Barbara;
Autschbach, Frank;
Funke, Benjamin;
Lasitschka, Felix;
Gassler, Nikolaus;
Fischer, Christine;
Whorwell, Peter J.;
Atkinson, Wendy;
Fell, Catherine;
Büchner, Karl J.;
Schmidtmann, Marco;
van der Voort, Ivo;
Wisser, Anna-Sophia;
Berg, Thomas

Publication type:

Article

Modulation of functional properties of laforin phosphatase by alternative splicing reveals a novel mechanism for the EPM2A gene in Lafora progressive myoclonus epilepsy.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3010, doi. 10.1093/hmg/ddn199

By:

Dubey, Deepti;
Ganesh, Subramaniam

Publication type:

Article

The 5q31 variants associated with psoriasis and Crohn's disease are distinct.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2978, doi. 10.1093/hmg/ddn196

By:

Li, Yonghong;
Chang, Monica;
Schrodi, Steven J.;
Callis-Duffin, Kristina P.;
Matsunami, Nori;
Civello, Daniel;
Bui, Nam;
Catanese, Joseph J.;
Leppert, Mark F.;
Krueger, Gerald G.;
Begovich, Ann B.

Publication type:

Article

Pharmacological manipulation of gain-of-function and dominant-negative mechanisms in rhodopsin retinitis pigmentosa.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3043, doi. 10.1093/hmg/ddn202

By:

Mendes, Hugo F.;
Cheetham, Michael E.

Publication type:

Article

A systematic RNAi screen reveals involvement of endocytic pathway in neuronal dysfunction in α-synuclein transgenic C. elegans.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2997, doi. 10.1093/hmg/ddn198

By:

Kuwahara, Tomoki;
Koyama, Akihiko;
Koyama, Shingo;
Yoshina, Sawako;
Ren, Chang-Hong;
Kato, Takeo;
Mitani, Shohei;
Iwatsubo, Takeshi

Publication type:

Article

Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3075, doi. 10.1093/hmg/ddn204

By:

Yanagi, Teruki;
Akiyama, Masashi;
Nishihara, Hiroshi;
Sakai, Kaori;
Nishie, Wataru;
Tanaka, Shinya;
Shimizu, Hiroshi

Publication type:

Article

The lamin B receptor under transcriptional control of C/EBPɛ is required for morphological but not functional maturation of neutrophils.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2921, doi. 10.1093/hmg/ddn191

By:

Cohen, Tatiana V.;
Klarmann, Kimberly D.;
Sakchaisri, Krisada;
Cooper, Jason P.;
Kuhns, Douglas;
Anver, Miriam;
Johnson, Peter F.;
Williams, Simon C.;
Keller, Jonathan R.;
Stewart, Colin L.

Publication type:

Article

Stabilization of β-catenin in XY gonads causes male-to-female sex-reversal.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2949, doi. 10.1093/hmg/ddn193

By:

Maatouk, Danielle M.;
DiNapoli, Leo;
Alvers, Ashley;
Parker, Keith L.;
Taketo, Makoto M.;
Capel, Blanche

Publication type:

Article

Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2986, doi. 10.1093/hmg/ddn197

By:

Warr, Nicholas;
Powles-Glover, Nicola;
Chappell, Anna;
Robson, Joan;
Norris, Dominic;
Arkell, Ruth M.

Publication type:

Article

Cytoplasmic and nuclear distribution of the protein complexes mTORC1 and mTORC2: rapamycin triggers dephosphorylation and delocalization of the mTORC2 components rictor and sin1.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2934, doi. 10.1093/hmg/ddn192

By:

Rosner, Margit;
Hengstschläger, Markus

Publication type:

Article

TDRD3, a novel Tudor domain-containing protein, localizes to cytoplasmic stress granules.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3055, doi. 10.1093/hmg/ddn203

By:

Goulet, Isabelle;
Boisvenue, Sophie;
Mokas, Sophie;
Mazroui, Rachid;
Côté, Jocelyn

Publication type:

Article

A large deletion in the human α-globin cluster caused by a replication error is associated with an unexpectedly mild phenotype.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3084, doi. 10.1093/hmg/ddn205

By:

Rugless, Michelle J.;
Fisher, Chris A.;
Old, John M.;
Sloane-Stanley, Jacqueline;
Ayyub, Helena;
Higgs, Douglas R.;
Garrick, David

Publication type:

Article

Neurofibromin regulates somatic growth through the hypothalamic–pituitary axis.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 2956, doi. 10.1093/hmg/ddn194

By:

Hegedus, Balazs;
Yeh, Tu-Hsueh;
Lee, Da Yong;
Emnett, Ryan J.;
Li, Jia;
Gutmann, David H.

Publication type:

Article

Three-dimensional conformation at the H19/Igf2 locus supports a model of enhancer tracking.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 19, p. 3021, doi. 10.1093/hmg/ddn200

By:

Engel, Nora;
Raval, Anjali K.;
Thorvaldsen, Joanne L.;
Bartolomei, S. Marisa

Publication type:

Article