Works matching IS 14345161 AND DT 2006 AND VI 51 AND IP 4

Results: 17

An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 284, doi. 10.1007/s10038-005-0358-1

By:

Nakashima, Kazuko;
Hirota, Tomomitsu;
Obara, Kazuhiko;
Shimizu, Makiko;
Jodo, Aya;
Kameda, Makoto;
Doi, Satoru;
Fujita, Kimie;
Shirakawa, Taro;
Enomoto, Tadao;
Kishi, Fumio;
Yoshihara, Shigemi;
Matsumoto, Kenji;
Saito, Hirohisa;
Suzuki, Yoichi;
Nakamura, Yusuke;
Tamari, Mayumi

Publication type:

Article

Microarray analysis of promoter methylation in lung cancers.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 368, doi. 10.1007/s10038-005-0355-4

By:

Fukasawa, Masayuki;
Kimura, Mika;
Morita, Sumiyo;
Matsubara, Kenichi;
Yamanaka, Sumitaka;
Endo, Chiaki;
Sakurada, Akira;
Sato, Masami;
Kondo, Takashi;
Horii, Akira;
Sasaki, Hiroyuki;
Hatada, Izuho

Publication type:

Article

Detection of novel Y SNPs provides further insights into Y chromosomal variation in Pakistan.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 375, doi. 10.1007/s10038-005-0357-2

By:

Mohyuddin, Aisha;
Ayub, Qasim;
Underhill, Peter A.;
Tyler-Smith, Chris;
Mehdi, S. Qasim

Publication type:

Article

Unified method for Bayesian calculation of genetic risk.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 387, doi. 10.1007/s10038-006-0371-z

By:

Kuno, Shin-ichi;
Furihata, Shiori;
Itou, Toshikazu;
Saito, Kayoko;
Kamatani, Naoyuki

Publication type:

Article

A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 379, doi. 10.1007/s10038-006-0360-2

By:

Kitanaka, Sachiko;
Takeda, Ayaka;
Sato, Utako;
Miki, Yuko;
Hishinuma, Akira;
Ieiri, Tamio;
Igarashi, Takashi

Publication type:

Article

The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 298, doi. 10.1007/s10038-006-0361-1

By:

Phasukkijwatana, Nopasak;
Chuenkongkaew, Wanicha;
Suphavilai, Rungnapa;
Suktitipat, Bhoom;
Pingsuthiwong, Sarinee;
Ruangvaravate, Ngamkae;
Atchaneeyasakul, La-ongsri;
Warrasak, Sukhuma;
Poonyathalang, Anuchit;
Sura, Thanyachai;
Lertrit, Patcharee

Publication type:

Article

Fifty years of genetic epidemiology, with special reference to Japan.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 269, doi. 10.1007/s10038-006-0366-9

By:

Morton, Newton E.

Publication type:

Article

Estimation of haplotype associated with several quantitative phenotypes based on maximization of area under a receiver operating characteristic (ROC) curve.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 314, doi. 10.1007/s10038-006-0363-z

By:

Kamitsuji, Shigeo;
Kamatani, Naoyuki

Publication type:

Article

The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 305, doi. 10.1007/s10038-006-0362-0

By:

Urreizti, Roser;
Asteggiano, Carla;
Bermudez, Marta;
Córdoba, Alfonso;
Szlago, Mariana;
Grosso, Carola;
de Kremer, Raquel Dodelson;
Vilarinho, Laura;
D'Almeida, Vania;
Martínez-Pardo, Mercedes;
Peña-Quintana, Luís;
Dalmau, Jaime;
Bernal, Jaime;
Briceño, Ignacio;
Couce, María;
Rodés, Marga;
Vilaseca, Maria;
Balcells, Susana;
Grinberg, Daniel

Publication type:

Article

MTHFR C677T and A1298C polymorphisms are risk factors for Down’s syndrome in Indian mothers.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 278, doi. 10.1007/s10038-005-0356-3

By:

Rai, Amit Kumar;
Singh, Satya;
Mehta, Stuti;
Kumar, Ashok;
Pandey, L. K.;
Raman, Rajiva

Publication type:

Article

Mutations of the puratrophin-1 ( PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 363, doi. 10.1007/s10038-006-0372-y

By:

Wieczorek, Stefan;
Arning, Larissa;
Alheite, Ingrid;
Epplen, Jörg

Publication type:

Article

Molecular characterization of a novel translocation t(5;14)(q21;q32) in a patient with congenital abnormalities.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 335, doi. 10.1007/s10038-006-0365-x

By:

Haider, Shawkat;
Matsumoto, Rie;
Kurosawa, Nobuyuki;
Wakui, Keiko;
Fukushima, Yoshimitsu;
Isobe, Masaharu

Publication type:

Article

Resequencing of the characterised CTGF gene to identify novel or known variants, and analysis of their association with diabetic nephropathy.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 383, doi. 10.1007/s10038-006-0368-7

By:

McKnight, Amy Jayne;
Savage, David A.;
Patterson, Chris C.;
Brady, Hugh R.;
Maxwell, A. Peter

Publication type:

Article

Identification of single nucleotide polymorphisms in FOXJ1 and their association with allergic rhinitis.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 292, doi. 10.1007/s10038-006-0359-8

By:

Chun-Shi Li;
Soo-Cheon Chae;
Jae-Hoon Lee;
Qinggao Zhang;
Hun-Taeg Chung

Publication type:

Article

Ancient retroviral insertions among human populations.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 353, doi. 10.1007/s10038-006-0370-0

By:

Herrera, Rene J.;
Lowery, Robert K.;
Alfonso, Abraham;
McDonald, John F.;
Luis, Javier R.

Publication type:

Article

TCR variable gene involvement in chromosome inversion between 14q11 and 14q24 in adult T-cell leukemia.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 326, doi. 10.1007/s10038-006-0364-y

By:

Haider, Shawkat;
Hayakawa, Kousuke;
Itoyama, Takahiro;
Sadamori, Naoki;
Kurosawa, Nobuyuki;
Isobe, Masaharu

Publication type:

Article

Corrective effect on Fabry mice of yeast recombinant human α-galactosidase with N-linked sugar chains suitable for lysosomal delivery.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 4, p. 341, doi. 10.1007/s10038-006-0369-6

By:

Sakuraba, Hitoshi;
Chiba, Yasunori;
Kotani, Masaharu;
Kawashima, Ikuo;
Ohsawa, Mai;
Tajima, Youichi;
Takaoka, Yuki;
Jigami, Yoshifumi;
Takahashi, Hiroshi;
Hirai, Yukihiko;
Shimada, Takashi;
Hashimoto, Yasuhiro;
Ishii, Kumiko;
Kobayashi, Toshihide;
Watabe, Kazuhiko;
Fukushige, Tomoko;
Kanzaki, Tamotsu

Publication type:

Article