Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 1

Results: 10

The first 17 amino acids of Huntingtin modulate its sub-cellular localization, aggregation and effects on calcium homeostasis.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 61, doi. 10.1093/hmg/ddl440
By:
- Rockabrand, Erica;
- Slepko, Natalia;
- Pantalone, Antonello;
- Nukala, Vidya N.;
- Kazantsev, Aleksey;
- Marsh, J. Lawrence;
- Sullivan, Patrick G.;
- Steffan, Joan S.;
- Sensi, Stefano L.;
- Thompson, Leslie Michels
Publication type:
Article
APC mutations in FAP-associated desmoid tumours are non-random but not ‘just right’.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 78, doi. 10.1093/hmg/ddl442
By:
- Latchford, Andrew;
- Volikos, Emmanouil;
- Johnson, Victoria;
- Rogers, Pauline;
- Suraweera, Nirosha;
- Tomlinson, Ian;
- Phillips, Robin;
- Silver, Andrew
Publication type:
Article
Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 36, doi. 10.1093/hmg/ddl438
By:
- Saccone, Scott F.;
- Hinrichs, Anthony L.;
- Saccone, Nancy L.;
- Chase, Gary A.;
- Konvicka, Karel;
- Madden, Pamela A.F.;
- Breslau, Naomi;
- Johnson, Eric O.;
- Hatsukami, Dorothy;
- Pomerleau, Ovide;
- Swan, Gary E.;
- Goate, Alison M.;
- Rutter, Joni;
- Bertelsen, Sarah;
- Fox, Louis;
- Fugman, Douglas;
- Martin, Nicholas G.;
- Montgomery, Grant W.;
- Wang, Jen C.;
- Ballinger, Dennis G.
Publication type:
Article
The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between β-amyloid production and tau phosphorylation in Alzheimer disease.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 15, doi. 10.1093/hmg/ddl437
By:
- Kimura, Ryo;
- Kamino, Kouzin;
- Yamamoto, Mitsuko;
- Nuripa, Aidaralieva;
- Kida, Tomoyuki;
- Kazui, Hiroaki;
- Hashimoto, Ryota;
- Tanaka, Toshihisa;
- Kudo, Takashi;
- Yamagata, Hidehisa;
- Tabara, Yasuharu;
- Miki, Tetsuro;
- Akatsu, Hiroyasu;
- Kosaka, Kenji;
- Funakoshi, Eishi;
- Nishitomi, Kouhei;
- Sakaguchi, Gaku;
- Kato, Akira;
- Hattori, Hideyuki;
- Uema, Takeshi
Publication type:
Article
Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 107, doi. 10.1093/hmg/ddl445
By:
- Weiss, Lauren A.;
- Purcell, Shaun;
- Waggoner, Skye;
- Lawrence, Kate;
- Spektor, David;
- Daly, Mark J.;
- Sklar, Pamela;
- Skuse, David
Publication type:
Article
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 1, doi. 10.1093/hmg/ddl436
By:
- Simon-Sanchez, Javier;
- Scholz, Sonja;
- Fung, Hon-Chung;
- Matarin, Mar;
- Hernandez, Dena;
- Gibbs, J. Raphael;
- Britton, Angela;
- de Vrieze, Fabienne Wavrant;
- Peckham, Elizabeth;
- Gwinn-Hardy, Katrina;
- Crawley, Anthony;
- Keen, Judith C.;
- Nash, Josefina;
- Borgaonkar, Digamber;
- Hardy, John;
- Singleton, Andrew
Publication type:
Article
Pael receptor induces death of dopaminergic neurons in the substantia nigra via endoplasmic reticulum stress and dopamine toxicity, which is enhanced under condition of parkin inactivation.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 50, doi. 10.1093/hmg/ddl439
By:
- Kitao, Yasuko;
- Imai, Yuzuru;
- Ozawa, Kentaro;
- Kataoka, Ayane;
- Ikeda, Toshio;
- Soda, Mariko;
- Nakimawa, Kazuhiko;
- Kiyama, Hiroshi;
- Stern, David M.;
- Hori, Osamu;
- Wakamatsu, Kazumasa;
- Ito, Shosuke;
- Itohara, Shigeyoshi;
- Takahashi, Ryosuke;
- Ogawa, Satoshi
Publication type:
Article
The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 92, doi. 10.1093/hmg/ddl444
By:
- Bitoun, Emmanuelle;
- Oliver, Peter L.;
- Davies, Kay E.
Publication type:
Article
Novel genes identified in a high-density genome wide association study for nicotine dependence.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 24, doi. 10.1093/hmg/ddl441
By:
- Bierut, Laura Jean;
- Madden, Pamela A.F.;
- Breslau, Naomi;
- Johnson, Eric O.;
- Hatsukami, Dorothy;
- Pomerleau, Ovide F.;
- Swan, Gary E.;
- Rutter, Joni;
- Bertelsen, Sarah;
- Fox, Louis;
- Fugman, Douglas;
- Goate, Alison M.;
- Hinrichs, Anthony L.;
- Konvicka, Karel;
- Martin, Nicholas G.;
- Montgomery, Grant W.;
- Saccone, Nancy L.;
- Saccone, Scott F.;
- Wang, Jen C.;
- Chase, Gary A.
Publication type:
Article
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 1, p. 83, doi. 10.1093/hmg/ddl443
By:
- Raux, Grégory;
- Bumsel, Emilie;
- Hecketsweiler, Bernadette;
- van Amelsvoort, Therese;
- Zinkstok, Janneke;
- Manouvrier-Hanu, Sylvie;
- Fantini, Carole;
- Brévière, Georges-Marie M.;
- Di Rosa, Gabriella;
- Pustorino, Giuseppina;
- Vogels, Annick;
- Swillen, Ann;
- Legallic, Solenn;
- Bou, Jacqueline;
- Opolczynski, Gaelle;
- Drouin-Garraud, Valérie;
- Lemarchand, Marie;
- Philip, Nicole;
- Gérard-Desplanches, Aude;
- Carlier, Michèle
Publication type:
Article