Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 13

Results: 12

In vivo maturation of human frataxin.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1534, doi. 10.1093/hmg/ddm102

By:

Condò, Ivano;
Ventura, Natascia;
Malisan, Florence;
Rufini, Alessandra;
Tomassini, Barbara;
Testi, Roberto

Publication type:

Article

p27Kip1 localization depends on the tumor suppressor protein tuberin.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1541, doi. 10.1093/hmg/ddm103

By:

Rosner, Margit;
Freilinger, Angelika;
Hanneder, Michaela;
Fujita, Naoya;
Lubec, Gert;
Tsuruo, Takashi;
Hengstschläger, Markus

Publication type:

Article

Gene expression fingerprinting for human hereditary hemorrhagic telangiectasia.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1515, doi. 10.1093/hmg/ddm069

By:

Fernandez-Lopez, Africa;
Garrido-Martin, Eva M.;
Sanz-Rodriguez, Francisco;
Pericacho, Miguel;
Rodriguez-Barbero, Alicia;
Eleno, Nelida;
Lopez-Novoa, Jose M.;
Düwell, Anette;
Vega, Miguel A.;
Bernabeu, Carmelo;
Botella, Luisa M.

Publication type:

Article

EGFR regulates RhoA-GTP dependent cell motility in E-cadherin mutant cells.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1639, doi. 10.1093/hmg/ddm113

By:

Mateus, Ana Rita;
Seruca, Raquel;
Machado, José Carlos;
Keller, Gisela;
Oliveira, Maria José;
Suriano, Gianpaolo;
Luber, Birgit

Publication type:

Article

Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1630, doi. 10.1093/hmg/ddm112

By:

Barlassina, Cristina;
Dal Fiume, Chiara;
Lanzani, Chiara;
Manunta, Paolo;
Guffanti, Guia;
Ruello, Antonella;
Bianchi, Giuseppe;
Del Vecchio, Lucia;
Macciardi, Fabio;
Cusi, Daniele

Publication type:

Article

CHRM2 variation predisposes to personality traits of agreeableness and conscientiousness.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1557, doi. 10.1093/hmg/ddm104

By:

Luo, Xingguang;
Kranzler, Henry R.;
Zuo, Lingjun;
Zhang, Huiping;
Wang, Shuang;
Gelernter, Joel

Publication type:

Article

Mutation of SOD1 in ALS: a gain of a loss of function.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1604, doi. 10.1093/hmg/ddm110

By:

Sau, Daniela;
De Biasi, Silvia;
Vitellaro-Zuccarello, Laura;
Riso, Patrizia;
Guarnieri, Serena;
Porrini, Marisa;
Simeoni, Silvia;
Crippa, Valeria;
Onesto, Elisa;
Palazzolo, Isabella;
Rusmini, Paola;
Bolzoni, Elena;
Bendotti, Caterina;
Poletti, Angelo

Publication type:

Article

L1 retrotransposition can occur early in human embryonic development.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1587, doi. 10.1093/hmg/ddm108

By:

van den Hurk, José A.J.M.;
Meij, Iwan C.;
del Carmen Seleme, Maria;
Kano, Hiroki;
Nikopoulos, Konstantinos;
Hoefsloot, Lies H.;
Sistermans, Erik A.;
de Wijs, Ilse J.;
Mukhopadhyay, Arijit;
Plomp, Astrid S.;
de Jong, Paulus T.V.M.;
Kazazian, Haig H.;
Cremers, Frans P.M.

Publication type:

Article

Akt blocks ligand binding and protects against expanded polyglutamine androgen receptor toxicity.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1593, doi. 10.1093/hmg/ddm109

By:

Palazzolo, Isabella;
Burnett, Barrington G.;
Young, Jessica E.;
Brenne, Phebe L.;
La Spada, Albert R.;
Fischbeck, Kenneth H.;
Howell, Brian W.;
Pennuto, Maria

Publication type:

Article

Ddb2 is a haploinsufficient tumor suppressor and controls spontaneous germ cell apoptosis.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1578, doi. 10.1093/hmg/ddm107

By:

Itoh, Toshiki;
Iwashita, Sachiyo;
Cohen, Michael B.;
Meyerholz, David K.;
Linn, Stuart

Publication type:

Article

LINE-1 retrotransposition in human embryonic stem cells.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1569, doi. 10.1093/hmg/ddm105

By:

Garcia-Perez, Jose L.;
Marchetto, Maria C.N.;
Muotri, Alysson R.;
Coufal, Nicole G.;
Gage, Fred H.;
O'Shea, K. Sue;
Moran, John V.

Publication type:

Article

Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 13, p. 1619, doi. 10.1093/hmg/ddm111

By:

Walne, Amanda J.;
Vulliamy, Tom;
Marrone, Anna;
Beswick, Richard;
Kirwan, Michael;
Masunari, Yuka;
Al-Qurashi, Fat-hia;
Aljurf, Mahmoud;
Dokal, Inderjeet

Publication type:

Article