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Journal of Human Genetics
|
May 29, 2015
Aggregation of rare/low-frequency variants of the mitochondria respiratory chain-related proteins in rheumatoid arthritis patients
Shigeki Mitsunaga, Kazuyoshi Hosomichi, Yuko Okudaira, et al.
Journal of Human Genetics
|
September 2, 2016
A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, Japan
Hideaki Kanzawa-Kiriyama, Kirill Kryukov, Timothy A Jinam, et al.
Human Genetics
|
May 21, 2008
Genome-wide association analysis with selective genotyping identifies candidate loci for adult height at 8q21.13 and 15q22.33-q23 in Mongolians
Tetsuaki Kimura, Terukazu Kobayashi, Batmunkh Munkhbat, et al.
Plos One
|
February 2, 2026
A SNP-based capture and clustering workflow to assess donor-derived cell-free DNA in transplantation
Shigeki Mitsunaga, Yohei Yamada, Phuong Thanh Nguyen, et al.
Cancer Science
|
June 3, 2009
Gene expression profiling of advanced-stage serous ovarian cancers distinguishes novel subclasses and implicates ZEB2 in tumor progression and prognosis
Kosuke Yoshihara, Atsushi Tajima, Dai Komata, et al.
Human Molecular Genetics
|
October 22, 2004
Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma: a candidate gene approach
Nobuyoshi Jinnai, Takuro Sakagami, Takashi Sekigawa, et al.
Journal of Human Genetics
|
November 1, 2013
A genome-wide association study of third molar agenesis in Japanese and Korean populations
Shugo Haga, Hirofumi Nakaoka, Tetsutaro Yamaguchi, et al.
Journal of Neuroinflammation
|
August 7, 2019
Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in Japanese
Kotaro Ogawa, Tatsusada Okuno, Kazuyoshi Hosomichi, et al.
Human Genome Variation
|
October 11, 2018
Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome
Kazumi Takahashi, Takahide Hayano, Ryota Sugimoto, et al.
Stroke and Vascular Neurology
|
April 23, 2025
Peripheral blood <i>GATA2</i> expression impacts <i>RNF213</i> mutation penetrance and clinical severity in moyamoya disease
Yohei Mineharu, Takahiko Kamata, Mei Tomoto, et al.
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Search research articles
Search
Showing results (121-130 of 175) with videos related to
Sort By:
Page
of 18
Journal of Human Genetics
|
May 29, 2015
Aggregation of rare/low-frequency variants of the mitochondria respiratory chain-related proteins in rheumatoid arthritis patients
Shigeki Mitsunaga, Kazuyoshi Hosomichi, Yuko Okudaira, et al.
Journal of Human Genetics
|
September 2, 2016
A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, Japan
Hideaki Kanzawa-Kiriyama, Kirill Kryukov, Timothy A Jinam, et al.
Human Genetics
|
May 21, 2008
Genome-wide association analysis with selective genotyping identifies candidate loci for adult height at 8q21.13 and 15q22.33-q23 in Mongolians
Tetsuaki Kimura, Terukazu Kobayashi, Batmunkh Munkhbat, et al.
Plos One
|
February 2, 2026
A SNP-based capture and clustering workflow to assess donor-derived cell-free DNA in transplantation
Shigeki Mitsunaga, Yohei Yamada, Phuong Thanh Nguyen, et al.
Cancer Science
|
June 3, 2009
Gene expression profiling of advanced-stage serous ovarian cancers distinguishes novel subclasses and implicates ZEB2 in tumor progression and prognosis
Kosuke Yoshihara, Atsushi Tajima, Dai Komata, et al.
Human Molecular Genetics
|
October 22, 2004
Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma: a candidate gene approach
Nobuyoshi Jinnai, Takuro Sakagami, Takashi Sekigawa, et al.
Journal of Human Genetics
|
November 1, 2013
A genome-wide association study of third molar agenesis in Japanese and Korean populations
Shugo Haga, Hirofumi Nakaoka, Tetsutaro Yamaguchi, et al.
Journal of Neuroinflammation
|
August 7, 2019
Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in Japanese
Kotaro Ogawa, Tatsusada Okuno, Kazuyoshi Hosomichi, et al.
Human Genome Variation
|
October 11, 2018
Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndrome
Kazumi Takahashi, Takahide Hayano, Ryota Sugimoto, et al.
Stroke and Vascular Neurology
|
April 23, 2025
Peripheral blood <i>GATA2</i> expression impacts <i>RNF213</i> mutation penetrance and clinical severity in moyamoya disease
Yohei Mineharu, Takahiko Kamata, Mei Tomoto, et al.
Page
of 18