Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 13

Results: 22

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2716, doi. 10.1093/hmg/ddq144
By:
- Macgregor, Stuart;
- Hewitt, Alex W.;
- Hysi, Pirro G.;
- Ruddle, Jonathan B.;
- Medland, Sarah E.;
- Henders, Anjali K.;
- Gordon, Scott D.;
- Andrew, Toby;
- McEvoy, Brian;
- Sanfilippo, Paul G.;
- Carbonaro, Francis;
- Tah, Vikas;
- Li, Yi Ju;
- Bennett, Sonya L.;
- Craig, Jamie E.;
- Montgomery, Grant W.;
- Tran-Viet, Khanh-Nhat;
- Brown, Nadean L.;
- Spector, Timothy D.;
- Martin, Nicholas G.
Publication type:
Article
Genome-wide association study of circulating vitamin D levels.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2739, doi. 10.1093/hmg/ddq155
By:
- Ahn, Jiyoung;
- Yu, Kai;
- Stolzenberg-Solomon, Rachael;
- Simon, K. Claire;
- McCullough, Marjorie L.;
- Gallicchio, Lisa;
- Jacobs, Eric J.;
- Ascherio, Alberto;
- Helzlsouer, Kathy;
- Jacobs, Kevin B.;
- Li, Qizhai;
- Weinstein, Stephanie J.;
- Purdue, Mark;
- Virtamo, Jarmo;
- Horst, Ronald;
- Wheeler, William;
- Chanock, Stephen;
- Hunter, David J.;
- Hayes, Richard B.;
- Kraft, Peter
Publication type:
Article
Genome-wide association of anthropometric traits in African- and African-derived populations.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2725, doi. 10.1093/hmg/ddq154
By:
- Kang, Sun J.;
- Chiang, Charleston W.K.;
- Palmer, Cameron D.;
- Tayo, Bamidele O.;
- Lettre, Guillaume;
- Butler, Johannah L.;
- Hackett, Rachel;
- Adeyemo, Adebowale A.;
- Guiducci, Candace;
- Berzins, Ilze;
- Nguyen, Thutrang T.;
- Feng, Tao;
- Luke, Amy;
- Shriner, Daniel;
- Ardlie, Kristin;
- Rotimi, Charles;
- Wilks, Rainford;
- Forrester, Terrence;
- McKenzie, Colin A.;
- Lyon, Helen N.
Publication type:
Article
ICI 182,780 induces P-cadherin overexpression in breast cancer cells through chromatin remodelling at the promoter level: a role for C/EBPβ in CDH3 gene activation.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2554, doi. 10.1093/hmg/ddq134
By:
- Albergaria, André;
- Ribeiro, Ana Sofia;
- Pinho, Sandra;
- Milanezi, Fernanda;
- Carneiro, Vítor;
- Sousa, Bárbara;
- Sousa, Sónia;
- Oliveira, Carla;
- Machado, José Carlos;
- Seruca, Raquel;
- Paredes, Joana;
- Schmitt, Fernando
Publication type:
Article
An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2682, doi. 10.1093/hmg/ddq158
By:
- Davies, Brandon S.J.;
- Barnes, Richard H.;
- Tu, Yiping;
- Ren, Shuxun;
- Andres, Douglas A.;
- Spielmann, H. Peter;
- Lammerding, Jan;
- Wang, Yibin;
- Young, Stephen G.;
- Fong, Loren G.
Publication type:
Article
High mitochondrial DNA copy number has detrimental effects in mice.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2695, doi. 10.1093/hmg/ddq163
By:
- Ylikallio, Emil;
- Tyynismaa, Henna;
- Tsutsui, Hiroyuki;
- Ide, Tomomi;
- Suomalainen, Anu
Publication type:
Article
Editorial Board.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. NP, doi. 10.1093/hmg/ddq219
Publication type:
Article
Genetic regulation of catecholamine synthesis, storage and secretion in the spontaneously hypertensive rat.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2567, doi. 10.1093/hmg/ddq135
By:
- Jirout, M.L.;
- Friese, R.S.;
- Mahapatra, N.R.;
- Mahata, M.;
- Taupenot, L.;
- Mahata, S.K.;
- Křen, V.;
- Zídek, V.;
- Fischer, J.;
- Maatz, H.;
- Ziegler, M.G.;
- Pravenec, M.;
- Hubner, N.;
- Aitman, T.J.;
- Schork, N.J.;
- O'Connor, D.T.
Publication type:
Article
Gene therapy rescues cone function in congenital achromatopsia.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2581
By:
- Komáromy, András M.;
- Alexander, John J.;
- Rowlan, Jessica S.;
- Garcia, Monique M.;
- Chiodo, Vince A.;
- Kaya, Asli;
- Tanaka, Jacqueline C.;
- Acland, Gregory M.;
- Hauswirth, William W.;
- Aguirre, Gustavo D.
Publication type:
Article
The nucleotide composition of microsatellites impacts both replication fidelity and mismatch repair in human colorectal cells.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2648, doi. 10.1093/hmg/ddq175
By:
- Campregher, Christoph;
- Scharl, Theresa;
- Nemeth, Manuela;
- Honeder, Clemens;
- Jascur, Thomas;
- Boland, C. Richard;
- Gasche, Christoph
Publication type:
Article
Visualizing Chromosome Mosaicism and Detecting Ethnic Outliers by the Method of “Rare” Heterozygotes and Homozygotes (RHH).
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2539, doi. 10.1093/hmg/ddq102
By:
- McGinnis, Ralph E.;
- Deloukas, Panos;
- McLaren, William M.;
- Inouye, Michael
Publication type:
Article
Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm†.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2630, doi. 10.1093/hmg/ddq150
By:
- Tong, Maoqing;
- Kato, Takema;
- Yamada, Kouji;
- Inagaki, Hidehito;
- Kogo, Hiroshi;
- Ohye, Tamae;
- Tsutsumi, Makiko;
- Wang, Jieru;
- Emanuel, Beverly S.;
- Kurahashi, Hiroki
Publication type:
Article
Cover Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. NP, doi. 10.1093/hmg/ddq218
Publication type:
Article
The STOX1 genotype associated with pre-eclampsia leads to a reduction of trophoblast invasion by α-T-catenin upregulation.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2658, doi. 10.1093/hmg/ddq152
By:
- van Dijk, Marie;
- van Bezu, Jan;
- van Abel, Daan;
- Dunk, Caroline;
- Blankenstein, Marinus A.;
- Oudejans, Cees B.M.;
- Lye, Stephen J.
Publication type:
Article
Reversal of neuropathy phenotypes in conditional mouse model of Charcot–Marie–Tooth disease type 2E.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2616, doi. 10.1093/hmg/ddq149
By:
- Dequen, Florence;
- Filali, Mohammed;
- Larivière, Roxanne C.;
- Perrot, Rodolphe;
- Hisanaga, Shin-Ichi;
- Julien, Jean-Pierre
Publication type:
Article
Zebrafish MTMR14 is required for excitation–contraction coupling, developmental motor function and the regulation of autophagy.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2668, doi. 10.1093/hmg/ddq153
By:
- Dowling, J.J.;
- Low, S.E.;
- Busta, A.S.;
- Feldman, E.L.
Publication type:
Article
Both microsatellite length and sequence context determine frameshift mutation rates in defective DNA mismatch repair.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2638, doi. 10.1093/hmg/ddq151
By:
- Chung, Heekyung;
- Lopez, Claudia G.;
- Holmstrom, Joy;
- Young, Dennis J.;
- Lai, Jenny F.;
- Ream-Robinson, Deena;
- Carethers, John M.
Publication type:
Article
Contents Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. NP, doi. 10.1093/hmg/ddq217
Publication type:
Article
Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2606, doi. 10.1093/hmg/ddq146
By:
- Chi, Zai-Long;
- Akahori, Masakazu;
- Obazawa, Minoru;
- Minami, Masayoshi;
- Noda, Toru;
- Nakaya, Naoki;
- Tomarev, Stanislav;
- Kawase, Kazuhide;
- Yamamoto, Tetsuya;
- Noda, Setsuko;
- Sasaoka, Masaki;
- Shimazaki, Atsushi;
- Takada, Yuichiro;
- Iwata, Takeshi
Publication type:
Article
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2706, doi. 10.1093/hmg/ddq156
By:
- Qi, Lu;
- Cornelis, Marilyn C.;
- Kraft, Peter;
- Stanya, Kristopher J.;
- Linda Kao, W.H.;
- Pankow, James S.;
- Dupuis, Josée;
- Florez, Jose C.;
- Fox, Caroline S.;
- Paré, Guillaume;
- Sun, Qi;
- Girman, Cynthia J.;
- Laurie, Cathy C.;
- Mirel, Daniel B.;
- Manolio, Teri A.;
- Chasman, Daniel I.;
- Boerwinkle, Eric;
- Ridker, Paul M.;
- Hunter, David J.;
- Meigs, James B.
Publication type:
Article
Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. 2594, doi. 10.1093/hmg/ddq145
By:
- O'Shaughnessy, Ryan F.L.;
- Choudhary, Ishaan;
- Harper, John I.
Publication type:
Article
Subscription Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 13, p. NP, doi. 10.1093/hmg/ddq220
Publication type:
Article