Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

نتائج البحث

Filter
  • 1-10 ل  20 نتائج ل ""Oligonucleotide Array Sequence Analysis""
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals.

  • Authors : Kawai Y; Department of Integrative Genomics, Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.; Graduate School of Medicine, Tohoku University, Sendai, Japan.

Subjects: Genotype* ; Haplotypes* ; Oligonucleotide Array Sequence Analysis*

  • Source: Journal of human genetics [J Hum Genet] 2015 Oct; Vol. 60 (10), pp. 581-7. Date of Electronic Publication: 2015 Jun 25.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

×
Academic Journal

Classification of sensitivity or resistance of cervical cancers to ionizing radiation according to expression profiles of 62 genes selected by cDNA microarray analysis.

  • Authors : Kitahara O; Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.; Katagiri T

Subjects: Gene Expression Profiling* ; Gene Expression Regulation, Neoplastic*/Gene Expression Regulation, Neoplastic*/Gene Expression Regulation, Neoplastic*/radiation effects ; Oligonucleotide Array Sequence Analysis*

  • Source: Neoplasia (New York, N.Y.) [Neoplasia] 2002 Jul-Aug; Vol. 4 (4), pp. 295-303.Publisher: Elsevier Country of Publication: United States NLM ID: 100886622 Publication Model: Print Cited Medium: Print ISSN: 1522-8002 (Print)

تفاصيل العنوان

×
Academic Journal

Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs.

  • Authors : Sakurai-Yageta M; Tohoku Medical Megabank Organization, Tohoku University, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8573, Japan.; Advanced Research Center for Innovations in Next-Generation Medicine, Tohoku University, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8573, Japan.

Subjects: Asian People/Asian People/Asian People/*genetics ; Genome-Wide Association Study/Genome-Wide Association Study/Genome-Wide Association Study/*methods ; Genotyping Techniques/Genotyping Techniques/Genotyping Techniques/*methods

  • Source: Journal of biochemistry [J Biochem] 2021 Oct 12; Vol. 170 (3), pp. 399-410.Publisher: Oxford University Press Country of Publication: England NLM ID: 0376600 Publication Model: Print Cited Medium: Internet ISSN:

تفاصيل العنوان

×
Academic Journal

Impact of visceral fat on gene expression profile in peripheral blood cells in obese Japanese subjects.

  • Authors : Obata Y; Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, 2-2-B5 Yamada-oka, Suita, Osaka, 565-0871, Japan.; Maeda N

Subjects: Adiposity*/Adiposity*/Adiposity*/ethnology ; Gene Expression Regulation*; Intra-Abdominal Fat/Intra-Abdominal Fat/Intra-Abdominal Fat/*physiopathology

  • Source: Cardiovascular diabetology [Cardiovasc Diabetol] 2016 Nov 29; Vol. 15 (1), pp. 159. Date of Electronic Publication: 2016 Nov 29.Publisher: BioMed Central Country of Publication: England NLM ID: 101147637 Publication Model: Electronic Cited Medium: Internet ISSN: 1475-2840

تفاصيل العنوان

×
Academic Journal

The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan.

  • Authors : Hirano M; Department of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Sakai, Japan; Department of Neurology, Kinki University Faculty of Medicine, Osakasayama, Japan.

Subjects: Bardet-Biedl Syndrome/Bardet-Biedl Syndrome/Bardet-Biedl Syndrome/*epidemiology; Adolescent ; Bardet-Biedl Syndrome/Bardet-Biedl Syndrome/Bardet-Biedl Syndrome/genetics

  • Source: PloS one [PLoS One] 2015 Sep 01; Vol. 10 (9), pp. e0136317. Date of Electronic Publication: 2015 Sep 01 (Print Publication: 2015).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

تفاصيل العنوان

×
Academic Journal

Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population.

  • Authors : Yamasaki M; Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.; Miyagawa T

Subjects: DNA Copy Number Variations* ; Genome-Wide Association Study*; Asian People/Asian People/Asian People/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2014 May; Vol. 59 (5), pp. 235-40. Date of Electronic Publication: 2014 Apr 03.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

×
Academic Journal

Single-nucleotide polymorphisms in the LRWD1 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome.

  • Authors : Miyamoto T; Department of Obstetrics and Gynecology, School of Medicine, Asahikawa Medical University, Asahikawa, Japan.; Koh E

Subjects: Polymorphism, Single Nucleotide*; Microtubule Proteins/Microtubule Proteins/Microtubule Proteins/*genetics ; Origin Recognition Complex/Origin Recognition Complex/Origin Recognition Complex/*genetics

  • Source: Andrologia [Andrologia] 2014 Apr; Vol. 46 (3), pp. 273-6. Date of Electronic Publication: 2013 Feb 28.Publisher: Blackwell Pub Country of Publication: Germany NLM ID: 0423506 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

×
Academic Journal

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.

  • Authors : Ishiura H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.; Takahashi Y

Subjects: Asian People/Asian People/Asian People/*genetics ; Mutation/Mutation/Mutation/*genetics ; Spastic Paraplegia, Hereditary/Spastic Paraplegia, Hereditary/Spastic Paraplegia, Hereditary/*epidemiology

  • Source: Journal of human genetics [J Hum Genet] 2014 Mar; Vol. 59 (3), pp. 163-72. Date of Electronic Publication: 2014 Jan 23.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

×
Academic Journal

Prediction of response to treatment by gene expression profiling of peripheral blood in patients with microscopic polyangiitis.

Subjects: Adrenal Cortex Hormones/Adrenal Cortex Hormones/Adrenal Cortex Hormones/*pharmacology ; Gene Expression Regulation/Gene Expression Regulation/Gene Expression Regulation/*drug effects ; Genetic Markers/Genetic Markers/Genetic Markers/*genetics

  • Source: PloS one [PLoS One] 2013 May 17; Vol. 8 (5), pp. e63182. Date of Electronic Publication: 2013 May 17 (Print Publication: 2013).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Electronic-Print Cited Medium: Internet

تفاصيل العنوان

×
Academic Journal

Copy-number variations observed in a Japanese population by BAC array CGH: summary of relatively rare CNVs.

  • Authors : Satoh Y; Department of Genetics, Radiation Effects Research Foundation, 5-2 Hijiyama Park, Minami-ku, Hiroshima 732-0815, Japan.; Sasaki K

Subjects: Heterozygote*; Chromosomes, Artificial, Bacterial/Chromosomes, Artificial, Bacterial/Chromosomes, Artificial, Bacterial/*genetics ; DNA Copy Number Variations/DNA Copy Number Variations/DNA Copy Number Variations/*genetics

  • Source: Journal of biomedicine & biotechnology [J Biomed Biotechnol] 2012; Vol. 2012, pp. 789024. Date of Electronic Publication: 2012 Jan 24.Publisher: Hindawi Pub. Corp Country of Publication: United States NLM ID: 101135740 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

×
  • 1-10 ل  20 نتائج ل ""Oligonucleotide Array Sequence Analysis""