Works matching IS 09646906 AND DT 2003 AND VI 12 AND IP 19

Results: 15

X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2559, doi. 10.1093/hmg/ddg268

By:

Hansen, R. Scott

Publication type:

Article

Increased expression of the glial glutamate transporter EAAT2 modulates excitotoxicity and delays the onset but not the outcome of ALS in mice.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2519, doi. 10.1093/hmg/ddg267

By:

Guo, Hong;
Lai, Liching;
Butchbach, Matthew E.R.;
Stockinger, Michael P.;
Shan, Xiu;
Bishop, Georgia A.;
Lin, Chien-liang Glenn

Publication type:

Article

A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2533, doi. 10.1093/hmg/ddg255

By:

Kao, Jau-Tsuen;
Wen, Hui-Chin;
Chien, Kuo-Liong;
Hsu, Hey-Chi;
Lin, Shu-Wha

Publication type:

Article

Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2503, doi. 10.1093/hmg/ddg266

By:

Hussain, Shobbir;
Witt, Emily;
Huber, Pia A.J.;
Medhurst, Annette L.;
Ashworth, Alan;
Mathew, Christopher G.

Publication type:

Article

Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased α7 integrin, utrophin and associated glycoproteins.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2467, doi. 10.1093/hmg/ddg264

By:

Moghadaszadeh, Behzad;
Albrechtsen, Reidar;
Guo, Ling T.;
Zaik, Michaela;
Kawaguchi, Nobuko;
Borup, Rehannah H.;
Kronqvist, Pauliina;
Schröder, Henrik D.;
Davies, Kay E.;
Voit, Thomas;
Nielsen, Finn C.;
Engvall, Eva;
Wewer, Ulla M.

Publication type:

Article

Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2547, doi. 10.1093/hmg/ddg263

By:

Chen, Li-Yuan;
Shieh, Jeng-Jer;
Lin, Baochuan;
Pan, Chi-Jiunn;
Gao, Ji-Liang;
Murphy, Philip M.;
Roe, Thomas F.;
Moses, Shimon;
Ward, Jerrold M.;
Lee, Eric J.;
Westphal, Heiner;
Mansfield, Brian C.;
Chou, Janice Yang

Publication type:

Article

Association of TNF-α promoter polymorphisms with the clearance of hepatitis B virus infection.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2541, doi. 10.1093/hmg/ddg262

By:

Kim, Yoon Jun;
Lee, Hyo-Suk;
Yoon, Jung-Hwan;
Kim, Chung Yong;
Park, Myoung Hee;
Kim, Lyoung Hyo;
Park, Byung Lae;
Shin, Hyoung Doo

Publication type:

Article

Valproic acid increases the SMN2 protein level: a well-known drug as a potential therapy for spinal muscular atrophy.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2481, doi. 10.1093/hmg/ddg256

By:

Brichta, L.;
Hofmann, Y.;
Hahnen, E.;
Siebzehnrubl, F. A.;
Raschke, H.;
Blumcke, I.;
Eyupoglu, I. Y.;
Wirth, B.

Publication type:

Article

Gene expression changes presage neurodegeneration in a Drosophila model of Parkinson's disease.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2457, doi. 10.1093/hmg/ddg265

By:

Scherzer, Clemens R.;
Jensen, Roderick V.;
Gullans, Steven R.;
Feany, Mel B.

Publication type:

Article

Significant linkage to migraine with aura on chromosome 11q24.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2511, doi. 10.1093/hmg/ddg252

By:

Cader, Zameel M.;
Noble-Topham, Sandra;
Dyment, David A.;
Cherny, Stacey S.;
Brown, John D.;
Rice, George P.A.;
Ebers, George C.

Publication type:

Article

A unification of mosaic structures in the human genome.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2411, doi. 10.1093/hmg/ddg251

By:

Lercher, Martin J.;
Urrutia, Araxi O.;
Pavlíček, Adam;
Hurst, Laurence D.

Publication type:

Article

Lowe syndrome protein OCRL1 interacts with Rac GTPase in the trans-Golgi network.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2449, doi. 10.1093/hmg/ddg250

By:

Faucherre, Adèle;
Desbois, Pierrette;
Satre, Véronique;
Lunardi, Joël;
Dorseuil, Olivier;
Gacon, Gérard

Publication type:

Article

Complexin II is essential for normal neurological function in mice.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2431, doi. 10.1093/hmg/ddg249

By:

Glynn, Dervila;
Bortnick, Rachel A.;
Morton, A. Jennifer

Publication type:

Article

Identification of SATB2 as the cleft palate gene on 2q32–q33.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2491, doi. 10.1093/hmg/ddg248

By:

FitzPatrick, David R.;
Carr, Ian M.;
McLaren, Lorna;
Leek, Jack P.;
Wightman, Patrick;
Williamson, Kathy;
Gautier, Philippe;
McGill, Niolette;
Hayward, Caroline;
Firth, Helen;
Markham, Alex F.;
Fantes, Judy A.;
Bonthron, David T.

Publication type:

Article

LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 19, p. 2417, doi. 10.1093/hmg/ddg247

By:

Bitoun, Emmanuelle;
Micheloni, Alessia;
Lamant, Laurence;
Bonnart, Chrystelle;
Tartaglia-Polcini, Alessandro;
Cobbold, Christian;
Al Saati, Talal;
Mariotti, Feliciana;
Mazereeuw-Hautier, Juliette;
Boralevi, Franck;
Hohl, Daniel;
Harper, John;
Bodemer, Christine;
D'Alessio, Marina;
Hovnanian, Alain

Publication type:

Article