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The Journal of Molecular Diagnostics : JMD
|
February 1, 2005
Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1)
Hiroyuki Nakamura, Daisuke Sawamura, Maki Goto, et al.
The American Journal of Pathology
|
January 1, 2010
Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen
Gang Wang, Hideyuki Ujiie, Akihiko Shibaki, et al.
Nature Medicine
|
February 27, 2007
Humanization of autoantigen
Wataru Nishie, Daisuke Sawamura, Maki Goto, et al.
Medicine
|
September 10, 2022
The impact of visual cross-modal conflict with semantic and nonsemantic distractors on working memory task: A functional near-infrared spectroscopy study
Daisuke Sawamura, Yoshinobu Tanabe, Satoshi Sakuraba, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 28, 2010
Bone marrow transplantation restores epidermal basement membrane protein expression and rescues epidermolysis bullosa model mice
Yasuyuki Fujita, Riichiro Abe, Daisuke Inokuma, et al.
The Australasian Journal of Dermatology
|
November 11, 2011
Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen
John Frew, Shueh W Lim, Alfred Klausseger, et al.
The Journal of Clinical Investigation
|
July 12, 2005
Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer
Masashi Akiyama, Yoriko Sugiyama-Nakagiri, Kaori Sakai, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 28, 2007
Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders
Kayo Sato-Jin, Emi K Nishimura, Eijiro Akasaka, et al.
Plos One
|
January 20, 2022
Enhanced β-adrenergic response in mice with dominant-negative expression of the PKD2L1 channel
Manabu Murakami, Agnieszka M Murakami, Takayuki Nemoto, et al.
Journal of Dermatological Science
|
April 11, 2018
In-frame Val<sup>216</sup>-Ser<sup>217</sup> deletion of KIT in mild piebaldism causes aberrant secretion and SCF response
Mai Hattori, Osamu Ishikawa, Daisuke Oikawa, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 161) with videos related to
Sort By:
Page
of 17
The Journal of Molecular Diagnostics : JMD
|
February 1, 2005
Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1)
Hiroyuki Nakamura, Daisuke Sawamura, Maki Goto, et al.
The American Journal of Pathology
|
January 1, 2010
Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen
Gang Wang, Hideyuki Ujiie, Akihiko Shibaki, et al.
Nature Medicine
|
February 27, 2007
Humanization of autoantigen
Wataru Nishie, Daisuke Sawamura, Maki Goto, et al.
Medicine
|
September 10, 2022
The impact of visual cross-modal conflict with semantic and nonsemantic distractors on working memory task: A functional near-infrared spectroscopy study
Daisuke Sawamura, Yoshinobu Tanabe, Satoshi Sakuraba, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 28, 2010
Bone marrow transplantation restores epidermal basement membrane protein expression and rescues epidermolysis bullosa model mice
Yasuyuki Fujita, Riichiro Abe, Daisuke Inokuma, et al.
The Australasian Journal of Dermatology
|
November 11, 2011
Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen
John Frew, Shueh W Lim, Alfred Klausseger, et al.
The Journal of Clinical Investigation
|
July 12, 2005
Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer
Masashi Akiyama, Yoriko Sugiyama-Nakagiri, Kaori Sakai, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 28, 2007
Epistatic connections between microphthalmia-associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders
Kayo Sato-Jin, Emi K Nishimura, Eijiro Akasaka, et al.
Plos One
|
January 20, 2022
Enhanced β-adrenergic response in mice with dominant-negative expression of the PKD2L1 channel
Manabu Murakami, Agnieszka M Murakami, Takayuki Nemoto, et al.
Journal of Dermatological Science
|
April 11, 2018
In-frame Val<sup>216</sup>-Ser<sup>217</sup> deletion of KIT in mild piebaldism causes aberrant secretion and SCF response
Mai Hattori, Osamu Ishikawa, Daisuke Oikawa, et al.
Page
of 17