Works matching IS 14345161 AND DT 2001 AND VI 46 AND IP 6

Results: 10

Development of genetic hypotheses in essential hypertension.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 299, doi. 10.1007/s100380170063
By:
- Lalouel, J.-M.;
- Rohrwasser, A.
Publication type:
Article
Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant Connexin 32 (GJB1).
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 307, doi. 10.1007/s100380170064
By:
- Matsuyama, W.;
- Nakagawa, M.;
- Moritoyo, T.;
- Takashima, H.;
- Umehara, F.;
- Hirata, K.;
- Suehara, M.;
- Osame, M.
Publication type:
Article
Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1, and L1CAM in the Japanese population.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 314, doi. 10.1007/s100380170065
By:
- Sekine, A.;
- Saito, S.;
- Iida, A.;
- Mitsunobu, Y.;
- Higuchi, S.;
- Harigae, S.;
- Nakamura, Y.
Publication type:
Article
Polymorphisms in PNLIP, encoding pancreatic lipase, and associations with metabolic traits.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 320, doi. 10.1007/s100380170066
By:
- Hegele, R. A.;
- Ramdath, D. D.;
- Ban, M. R.;
- Carruthers, M. N.;
- Carrington, C. V.;
- Cao, H.
Publication type:
Article
Seventy genetic variations in human microsomal and soluble epoxide hydrolase genes (EPHX1 and EPHX2) in the Japanese population.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 325, doi. 10.1007/s100380170067
By:
- Saito, S.;
- Iida, A.;
- Sekine, A.;
- Eguchi, C.;
- Miura, Y.;
- Nakamura, Y.
Publication type:
Article
Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA[sup Leu(UUR)] gene in Japanese patients with diabetes mellitus and end stage renal disease.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 330, doi. 10.1007/s100380170068
By:
- Iwasaki, N.;
- Babazono, T.;
- Tsuchiya, K.;
- Tomonaga, O.;
- Suzuki, A.;
- Togashi, M.;
- Ujihara, N.;
- Sakka, Y.;
- Yokokawa, H.;
- Ogata, M.;
- Nihei, H.;
- Iwamoto, Y.
Publication type:
Article
Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 335, doi. 10.1007/s100380170069
By:
- Kayahara, H.;
- Yamagata, H.;
- Tanioka, H.;
- Miki, T.;
- Hamakawa, H.
Publication type:
Article
Human arylhydrocarbon receptor repressor (AHRR) gene: genomic structure and analysis of polymorphism in endometriosis.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 342, doi. 10.1007/s100380170070
By:
- Watanabe, T.;
- Imoto, I.;
- Kosugi, Y.;
- Fukuda, Y.;
- Mimura, J.;
- Fujii, Y.;
- Isaka, K.;
- Takayama, M.;
- Sato, A.;
- Inazawa, J.
Publication type:
Article
Parental age and the origin of extra chromosome 21 in Down syndrome.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 347, doi. 10.1007/s100380170071
By:
- Jyothy, A.;
- Kumar, K. S. D.;
- Rao, G.N. Mallikarjuna;
- Rao, V. Babu;
- Devi, B. Uma;
- Sujatha, M.;
- Reddy, P. P.
Publication type:
Article
Single-nucleotide polymorphisms of the nuclear lamina proteome.
Published in:
Journal of Human Genetics, 2001, v. 46, n. 6, p. 351
By:
- Hegele, R. A.;
- Yuen, J.;
- Cao, H.
Publication type:
Article