Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 9

Results: 17

Polymorphisms in interleukin 8 and its receptors ( IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 781, doi. 10.1007/s10038-006-0021-5

By:

Cheong, Hyun Sub;
Shin, Hyoung Doo;
Lee, Soo Ok;
Park, Byung Lae;
Choi, Yoo Hyun;
Lim, Gun Il;
Uh, Soo Taek;
Kim, Young Hun;
Lee, Jong-Young;
Lee, Jong-Keuk;
Kim, Hung Tae;
Ryu, Ha-Jung;
Kim, Ka-Kyung;
Han, Bok Ghee;
Kim, Jun Woo;
Kimm, Kuchan;
Oh, Bermseok;
Park, Choon-Sik

Publication type:

Article

Functional analysis of PKHD1 splicing in autosomal recessive polycystic kidney disease.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 788, doi. 10.1007/s10038-006-0022-4

By:

Bergmann, Carsten;
Frank, Valeska;
Küpper, Fabian;
Schmidt, Christa;
Senderek, Jan;
Zerres, Klaus

Publication type:

Article

Refinement of the locus for autosomal recessive cone–rod dystrophy (CORD8) linked to chromosome 1q23–q24 in a Pakistani family and exclusion of candidate genes.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 827, doi. 10.1007/s10038-006-0028-y

By:

Ismail, Muhammad;
Abid, Aiysha;
Anwar, Khalid;
Mehdi, S. Qasim;
Khaliq, Shagufta

Publication type:

Article

Frequent DAP kinase but not p14 or Apaf-1 hypermethylation in B-cell chronic lymphocytic leukemia.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 832, doi. 10.1007/s10038-006-0029-x

By:

Chim, C. S.;
Fung, T. K.;
Wong, K. F.;
Lau, J. S.;
Liang, R.

Publication type:

Article

Longevity-associated NADH dehydrogenase subunit-2 237 Leu/Met polymorphism influences the effects of alcohol consumption on serum uric acid levels in nonobese Japanese men.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 765, doi. 10.1007/s10038-006-0018-0

By:

Kokaze, Akatsuki;
Ishikawa, Mamoru;
Matsunaga, Naomi;
Yoshida, Masao;
Satoh, Masao;
Teruya, Koji;
Honmyo, Rie;
Yorimitsu, Misako;
Masuda, Yumi;
Uchida, Yoshiko;
Takashima, Yutaka

Publication type:

Article

An algorithm for model construction and its applications to pharmacogenomic studies.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 751, doi. 10.1007/s10038-006-0016-2

By:

Liang, Kung-Hao;
Hwang, Yuchi;
Shao, Wan-Ching;
Chen, Ellson Y.

Publication type:

Article

A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 760, doi. 10.1007/s10038-006-0017-1

By:

Gul, Asma;
Hassan, Muhammad Jawad;
Hussain, Sabir;
Raza, Syed Irfan;
Chishti, Muhammad Salman;
Ahmad, Wasim

Publication type:

Article

Study of AZFc partial deletion gr/gr in fertile and infertile Japanese males.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 794, doi. 10.1007/s10038-006-0024-2

By:

de Carvalho, Cláudia Márcia Benedetto;
Zuccherato, Luciana Werneck;
Fujisawa, Masato;
Shirakawa, Toshiro;
Ribeiro-dos-Santos, Andrea Kely Campos;
Santos, Sidney, E. B.;
Pena, Sérgio Danilo Junho;
Santos, Fabrício Rodrigues

Publication type:

Article

Pure de-novo 5 Mb duplication at Xp11.22–p11.23 in a male: phenotypic and molecular characterization.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 815, doi. 10.1007/s10038-006-0023-3

By:

Bonnet, C.;
Grégoire, M. J.;
Brochet, K.;
Raffo, E.;
Leheup, B.;
Jonveaux, P.

Publication type:

Article

Pharmacogenetic determinants of variability in lipid-lowering response to pravastatin therapy.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 822, doi. 10.1007/s10038-006-0025-1

By:

Takane, Hiroshi;
Miyata, Masanori;
Burioka, Naoto;
Shigemasa, Chiaki;
Shimizu, Eiji;
Otsubo, Kenji;
Ieiri, Ichiro

Publication type:

Article

The confidence interval of allelic odds ratios under the Hardy–Weinberg disequilibrium.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 772, doi. 10.1007/s10038-006-0020-6

By:

Sato, Yasunori;
Suganami, Hideki;
Hamada, Chikuma;
Yoshimura, Isao;
Sakamoto, Hiromi;
Yoshida, Teruhiko;
Yoshimura, Kimio

Publication type:

Article

Unique origin of Andaman Islanders: insight from autosomal loci.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 800, doi. 10.1007/s10038-006-0026-0

By:

Thangaraj, K.;
Chaubey, G.;
Reddy, A. G.;
Singh, V. K.;
Singh, L.

Publication type:

Article

Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 805, doi. 10.1007/s10038-006-0027-z

By:

Iwasaki, Satoshi;
Tsukamoto, Koji;
Usami, Shinichi;
Misawa, Kiyoshi;
Mizuta, Kunihiro;
Mineta, Hiroyuki

Publication type:

Article

Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuoles.

Published in:

2006

By:

Kim, Byoung Joon;
Ki, Chang-Seok;
Kim, Jong-Won;
Sung, Duk Hyun;
Choi, Young-Chul;
Kim, Seung Hyun

Publication type:

Correction Notice

Role of B cell inhibitory receptor polymorphisms in systemic lupus erythematosus: a negative times a negative makes a positive.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 741, doi. 10.1007/s10038-006-0030-4

By:

Tsuchiya, Naoyuki;
Honda, Zen-ichiro;
Tokunaga, Katsushi

Publication type:

Article

Farber lipogranulomatosis: clinical and molecular genetic analysis reveals a novel mutation in an Indian family.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 9, p. 811, doi. 10.1007/s10038-006-0019-z

By:

Devi, Akela Radha Rama;
Gopikrishna, Munimanda;
Ratheesh, Raman;
Savithri, Gorinabele;
Swarnalata, Gowrishankar;
Bashyam, Murali

Publication type:

Article

Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa.

Published in:

2006

By:

Sawamura, Daisuke;
Goto, Maki;
Yasukawa, Kana;
Sato-Matsumura, Kazuko;
Nakamura, Hideki;
Ito, Kei;
Nakamura, Hiroyuki;
Tomita, Yuki;
Shimizu, Hiroshi

Publication type:

Correction Notice