Works matching IS 03406717 AND DT 2006 AND VI 120 AND IP 1

Results: 18

Efficient selection of tagging single-nucleotide polymorphisms in multiple populations.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 58, doi. 10.1007/s00439-006-0182-5

By:

Howie, Bryan N.;
Carlson, Christopher S.;
Rieder, Mark J.;
Nickerson, Deborah A.

Publication type:

Article

A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes I: general principles and overview.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 1, doi. 10.1007/s00439-006-0180-7

By:

Jian-Min Chen;
Férec, Claude;
Cooper, David

Publication type:

Article

Loss of function polymorphisms in NAT1 protect against spina bifida.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 52, doi. 10.1007/s00439-006-0181-6

By:

Jensen, Liselotte E.;
Hoess, Karen;
Mitchell, Laura E.;
Whitehead, Alexander S.

Publication type:

Article

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 85, doi. 10.1007/s00439-006-0188-z

By:

Santos, Regie Lyn P.;
Hassan, Muhammad Jawad;
Sikandar, Shaheen;
Kwanghyuk Lee;
Ali, Ghazanfar;
Martin Jr., Protacio E.;
Wambangco, Michael Angelo L.;
Ahmad, Wasim;
Leal, Suzanne M.

Publication type:

Article

A complex rearrangement on chromosome 22 affecting both homologues; haplo-insufficiency of the Cat eye syndrome region may have no clinical relevance.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 77, doi. 10.1007/s00439-006-0185-2

By:

Kriek, Marjolein;
Szuhai, Karoly;
Kant, Sarina G.;
White, Stefan J.;
Dauwerse, Hans;
Fiegler, Heike;
Carter, Nigel P.;
Knijnenburg, Jeroen;
den Dunnen, Johan T.;
Tanke, Hans J.;
Breuning, Martijn H.;
Rosenberg, Carla

Publication type:

Article

No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 139, doi. 10.1007/s00439-006-0187-0

By:

Gotoh, Norimoto;
Yamada, Ryo;
Hiratani, Hitomi;
Renault, Victor;
Kuroiwa, Sachiko;
Monet, Marion;
Toyoda, Sachiko;
Chida, Shohei;
Mandai, Michiko;
Otani, Atsushi;
Yoshimura, Nagahisa;
Matsuda, Fumihiko

Publication type:

Article

ITGB3 shows genetic and expression interaction with SLC6A4.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 93, doi. 10.1007/s00439-006-0196-z

By:

Weiss, Lauren A.;
Ober, Carole;
Cook Jr., Edwin H.

Publication type:

Article

The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 101, doi. 10.1007/s00439-006-0186-1

By:

Riessland, Markus;
Brichta, Lars;
Hahnen, Eric;
Wirth, Brunhilde

Publication type:

Article

ICAM gene cluster SNPs and prostate cancer risk in African Americans.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 69, doi. 10.1007/s00439-006-0184-3

By:

Hankui Chen;
Hernandez, Wenndy;
Shriver, Mark;
Ahaghotu, Chiledum;
Kittles, Rick

Publication type:

Article

Association analyses of CYP19 gene polymorphisms with height variation in a large sample of Caucasian nuclear families.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 119, doi. 10.1007/s00439-006-0199-9

By:

Tie-Lin Yang;
Dong-Hai Xiong;
Yan Guo;
Recker, Robert;
Hong-Wen Deng

Publication type:

Article

Meta-analysis shows association between the tryptophan hydroxylase ( TPH) gene and schizophrenia.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 22, doi. 10.1007/s00439-006-0190-5

By:

Dawei Li;
Lin He

Publication type:

Article

Cytogenetics of human germ cells.

Published in:

2006

By:

Delhanty, Joy D. A.

Publication type:

Book Review

Differential expression of the cardiac ryanodine receptor in normal and arrhythmogenic right ventricular cardiomyopathy canine hearts.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 111, doi. 10.1007/s00439-006-0193-2

By:

Meurs, Kathryn M.;
Lacombe, Veronique A.;
Dryburgh, Keith;
Fox, Philip R.;
Reiser, Peter R.;
Kittleson, Mark D.

Publication type:

Article

Strong association between polymorphisms in ANKH locus and skeletal size traits.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 42, doi. 10.1007/s00439-006-0173-6

By:

Malkin, Ida;
Ermakov, Sergey;
Kobyliansky, Eugene;
Livshits, Gregory

Publication type:

Article

A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2–q12.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 144, doi. 10.1007/s00439-006-0206-1

By:

Yongjia Yang;
Jihong Guo;
Zheng Liu;
Siyuan Tang;
Ningdong Li;
Mengrong Yang;
Qiong Pang;
Feiyue Fan;
Juan Bu;
Song Tao Yuan;
Xiangjun Xiao;
Yuxiang Chen;
Kanxing Zhao

Publication type:

Article

Characterization of the human lineage-specific pericentric inversion that distinguishes human chromosome 1 from the homologous chromosomes of the great apes.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 126, doi. 10.1007/s00439-006-0209-y

By:

Szamalek, Justyna;
Goidts, Violaine;
Cooper, David;
Hameister, Horst;
Kehrer-Sawatzki, Hildegard

Publication type:

Article

Announcement.

Published in:: Human Genetics, 2006, v. 120, n. 1, p. 150, doi. 10.1007/s00439-006-0208-z
Publication type:: Article

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.

Published in:

Human Genetics, 2006, v. 120, n. 1, p. 31, doi. 10.1007/s00439-006-0163-8

By:

Panhuysen, Carolien I.;
Karban, Amir;
Manning, Alisa Knodle;
Bayless, Theodore M.;
Duerr, Richard H.;
Bailey-Wilson, Joan E.;
Epstein Jr., Ervin H.;
Brant, Steven R.

Publication type:

Article