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