Works matching IS 03406717 AND DT 2010 AND VI 127 AND IP 3

Results: 10

The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 295, doi. 10.1007/s00439-009-0769-8

By:

Franceschini, Nora;
Voruganti, V. Saroja;
Haack, Karin;
Almasy, Laura;
Laston, Sandy;
Göring, Harald H. H.;
Umans, Jason G.;
Lee, Elisa T.;
Best, Lyle G.;
Fabsitz, Richard R.;
MacCluer, Jean W.;
Howard, Barbara V.;
North, Kari E.;
Cole, Shelley A.

Publication type:

Article

Jones S, Keynes M (eds): Twelve Galton lectures. A centenary selection with commentaries.

Published in:

2010

By:

Harper, Peter S.

Publication type:

Book Review

The Q223R polymorphism in LEPR is associated with obesity in Pacific Islanders.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 287, doi. 10.1007/s00439-009-0768-9

By:

Furusawa, Takuro;
Naka, Izumi;
Yamauchi, Taro;
Natsuhara, Kazumi;
Kimura, Ryosuke;
Nakazawa, Minato;
Ishida, Takafumi;
Inaoka, Tsukasa;
Matsumura, Yasuhiro;
Ataka, Yuji;
Nishida, Nao;
Tsuchiya, Naoyuki;
Ohtsuka, Ryutaro;
Ohashi, Jun

Publication type:

Article

A genome-wide association identified the common genetic variants influence disease severity in β<sup>0</sup>-thalassemia/hemoglobin E.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 303, doi. 10.1007/s00439-009-0770-2

By:

Nuinoon, Manit;
Makarasara, Wattanan;
Mushiroda, Taisei;
Setianingsih, Iswari;
Wahidiyat, Pustika Amalia;
Sripichai, Orapan;
Kumasaka, Natsuhiko;
Takahashi, Atsushi;
Svasti, Saovaros;
Munkongdee, Thongperm;
Mahasirimongkol, Surakameth;
Peerapittayamongkol, Chayanon;
Viprakasit, Vip;
Kamatani, Naoyuki;
Winichagoon, Pranee;
Kubo, Michiaki;
Nakamura, Yusuke;
Fucharoen, Suthat

Publication type:

Article

Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibility.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 337, doi. 10.1007/s00439-009-0775-x

By:

Alter, Andrea;
de Léséleuc, Louis;
Van Thuc, Nguyen;
Vu Hong Thai;
Nguyen Thu Huong;
Nguyen Ngoc Ba;
Cardoso, Cynthia Chester;
Grant, Audrey Virginia;
Abel, Laurent;
Moraes, Milton Ozório;
Alcaïs, Alexandre;
Schurr, Erwin

Publication type:

Article

Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 325, doi. 10.1007/s00439-009-0777-8

By:

LopezJimenez, Nelson;
Gerber, Simon;
Popovici, Vlad;
Mirza, Sonia;
Copren, Kirsten;
Ta, Linda;
Shaw, Gary M.;
Trueb, Beat;
Slavotinek, Anne M.

Publication type:

Article

Large intron 14 rearrangement in APC results in splice defect and attenuated FAP.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 359, doi. 10.1007/s00439-009-0776-9

By:

Tuohy, Thérèse M. F.;
Done, Michelle W.;
Lewandowski, Michelle S.;
Shires, Patricia M.;
Saraiya, Devki S.;
Huang, Sherry C.;
Neklason, Deborah W.;
Burt, Randall W.

Publication type:

Article

Effects of measured susceptibility genes on cancer risk in family studies.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 349, doi. 10.1007/s00439-009-0774-y

By:

Chih-Chieh Wu;
Strong, Louise C.;
Shete, Sanjay

Publication type:

Article

Genetics of osteoporosis: accelerating pace in gene identification and validation.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 249, doi. 10.1007/s00439-009-0773-z

By:

Wen-Feng Li;
Shu-Xun Hou;
Bin Yu;
Meng-Meng Li;
Férec, Claude;
Jian-Min Chen

Publication type:

Article

SNPs for a universal individual identification panel.

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 315, doi. 10.1007/s00439-009-0771-1

By:

Pakstis, Andrew J.;
Speed, William C.;
Rixun Fang;
Hyland, Fiona C. L.;
Furtado, Manohar R.;
Kidd, Judith R.;
Kidd, Kenneth K.

Publication type:

Article