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Journal of Immunology (Baltimore, Md. : 1950)
|
February 25, 2005
Suppressors of cytokine signaling-1 and -3 regulate osteoclastogenesis in the presence of inflammatory cytokines
Masanobu Ohishi, Yumiko Matsumura, Daisuke Aki, et al.
Molecular Genetics and Metabolism Reports
|
November 11, 2017
A molecular analysis of the GAA gene and clinical spectrum in 38 patients with Pompe disease in Japan
Yasuyuki Fukuhara, Naoko Fuji, Narutoshi Yamazaki, et al.
The Journal of Biological Chemistry
|
December 31, 2003
SOCS3 is a physiological negative regulator for granulopoiesis and granulocyte colony-stimulating factor receptor signaling
Akiko Kimura, Ichiko Kinjyo, Yumiko Matsumura, et al.
The Journal of Biological Chemistry
|
October 14, 2005
FLN29, a novel interferon- and LPS-inducible gene acting as a negative regulator of toll-like receptor signaling
Ryuichi Mashima, Kazuko Saeki, Daisuke Aki, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 22, 2005
Induction of hyper Th1 cell-type immune responses by dendritic cells lacking the suppressor of cytokine signaling-1 gene
Toshikatsu Hanada, Kentaro Tanaka, Yumiko Matsumura, et al.
Journal of Cellular Physiology
|
July 7, 2011
Dok-1 and Dok-2 deficiency induces osteopenia via activation of osteoclasts
Aya Kawamata, Akane Inoue, Daisuke Miyajima, et al.
Nature Medicine
|
June 23, 2004
Socs3 deficiency in the brain elevates leptin sensitivity and confers resistance to diet-induced obesity
Hiroyuki Mori, Reiko Hanada, Toshikatsu Hanada, et al.
The American Journal of Pathology
|
February 13, 2002
Disease stage-dependent accumulation of lipid and protein oxidation products in human atherosclerosis
Joanne M Upston, Xianwa Niu, Andrew J Brown, et al.
Molecular Genetics and Metabolism
|
June 2, 2016
Molecular diagnosis of 65 families with mucopolysaccharidosis type II (Hunter syndrome) characterized by 16 novel mutations in the IDS gene: Genetic, pathological, and structural studies on iduronate-2-sulfatase
Motomichi Kosuga, Ryuichi Mashima, Asami Hirakiyama, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
June 16, 2010
Mice lacking Dok-1, Dok-2, and Dok-3 succumb to aggressive histiocytic sarcoma
Ryuichi Mashima, Kazuho Honda, Yi Yang, et al.
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of 5
Search research articles
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Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Journal of Immunology (Baltimore, Md. : 1950)
|
February 25, 2005
Suppressors of cytokine signaling-1 and -3 regulate osteoclastogenesis in the presence of inflammatory cytokines
Masanobu Ohishi, Yumiko Matsumura, Daisuke Aki, et al.
Molecular Genetics and Metabolism Reports
|
November 11, 2017
A molecular analysis of the GAA gene and clinical spectrum in 38 patients with Pompe disease in Japan
Yasuyuki Fukuhara, Naoko Fuji, Narutoshi Yamazaki, et al.
The Journal of Biological Chemistry
|
December 31, 2003
SOCS3 is a physiological negative regulator for granulopoiesis and granulocyte colony-stimulating factor receptor signaling
Akiko Kimura, Ichiko Kinjyo, Yumiko Matsumura, et al.
The Journal of Biological Chemistry
|
October 14, 2005
FLN29, a novel interferon- and LPS-inducible gene acting as a negative regulator of toll-like receptor signaling
Ryuichi Mashima, Kazuko Saeki, Daisuke Aki, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
March 22, 2005
Induction of hyper Th1 cell-type immune responses by dendritic cells lacking the suppressor of cytokine signaling-1 gene
Toshikatsu Hanada, Kentaro Tanaka, Yumiko Matsumura, et al.
Journal of Cellular Physiology
|
July 7, 2011
Dok-1 and Dok-2 deficiency induces osteopenia via activation of osteoclasts
Aya Kawamata, Akane Inoue, Daisuke Miyajima, et al.
Nature Medicine
|
June 23, 2004
Socs3 deficiency in the brain elevates leptin sensitivity and confers resistance to diet-induced obesity
Hiroyuki Mori, Reiko Hanada, Toshikatsu Hanada, et al.
The American Journal of Pathology
|
February 13, 2002
Disease stage-dependent accumulation of lipid and protein oxidation products in human atherosclerosis
Joanne M Upston, Xianwa Niu, Andrew J Brown, et al.
Molecular Genetics and Metabolism
|
June 2, 2016
Molecular diagnosis of 65 families with mucopolysaccharidosis type II (Hunter syndrome) characterized by 16 novel mutations in the IDS gene: Genetic, pathological, and structural studies on iduronate-2-sulfatase
Motomichi Kosuga, Ryuichi Mashima, Asami Hirakiyama, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
June 16, 2010
Mice lacking Dok-1, Dok-2, and Dok-3 succumb to aggressive histiocytic sarcoma
Ryuichi Mashima, Kazuho Honda, Yi Yang, et al.
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of 5