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Michihiro Kono

Showing results (21-30 of 79) with videos related to

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American Journal of Human Genetics|August 14, 2003
Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditariaYoshinori Miyamura, Tamio Suzuki, Michihiro Kono, et al.
Internal Medicine (Tokyo, Japan)|June 16, 2020
Non-tuberculosis Mycobacterium Tenosynovitis with Rice Bodies in a Patient with Systemic Lupus ErythematosusYuichiro Fujieda, Keita Ninagawa, Yuichiro Matsui, et al.
Internal Medicine (Tokyo, Japan)|December 4, 2024
Cutaneous Squamous Cell Carcinoma Producing Granulocyte Colony-stimulating Factor and Parathyroid Hormone-related Protein: A Case Report and Literature ReviewTakuya Kumagai, Masaya Saito, Takahiko Sato, et al.
International Journal of Dermatology|May 31, 2014
Proposed classification of longitudinal melanonychia based on clinical and dermoscopic criteriaMasaki Sawada, Kenji Yokota, Takaaki Matsumoto, et al.
American Journal of Ophthalmology|April 29, 2023
Different patterns in the corneal endothelial cell loss after pars plana and pars limbal insertion of the Baerveldt glaucoma implantEtsuo Chihara, Masaki Tanito, Michihiro Kono, et al.
The Journal of Dermatology|August 19, 2008
Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypesTaisuke Kondo, Tamio Suzuki, Yoshihiko Mitsuhashi, et al.
Journal of Dermatological Science|February 23, 2002
A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1)Eriko Nakamura, Yoshinori Miyamura, Jun Matsunaga, et al.
The American Journal of Dermatopathology|August 1, 2020
MYB Translocations in Both Myoepithelial and Ductoglandular Epithelial Cells in Adenoid Cystic Carcinoma: A Histopathologic and Genetic Reappraisal in Six Primary Cutaneous CasesKeisuke Goto, Kazuyoshi Kajimoto, Takashi Sugino, et al.
Journal of Dermatological Science|August 28, 2023
Eosinophil-derived galectin-10 upregulates matrix metalloproteinase expression in bullous pemphigoid blistersTakahiko Sato, Takahito Chiba, Takeshi Nakahara, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2Takayuki Konno, Yuko Abe, Masakazu Kawaguchi, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|August 14, 2003
Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditariaYoshinori Miyamura, Tamio Suzuki, Michihiro Kono, et al.
Internal Medicine (Tokyo, Japan)|June 16, 2020
Non-tuberculosis Mycobacterium Tenosynovitis with Rice Bodies in a Patient with Systemic Lupus ErythematosusYuichiro Fujieda, Keita Ninagawa, Yuichiro Matsui, et al.
Internal Medicine (Tokyo, Japan)|December 4, 2024
Cutaneous Squamous Cell Carcinoma Producing Granulocyte Colony-stimulating Factor and Parathyroid Hormone-related Protein: A Case Report and Literature ReviewTakuya Kumagai, Masaya Saito, Takahiko Sato, et al.
International Journal of Dermatology|May 31, 2014
Proposed classification of longitudinal melanonychia based on clinical and dermoscopic criteriaMasaki Sawada, Kenji Yokota, Takaaki Matsumoto, et al.
American Journal of Ophthalmology|April 29, 2023
Different patterns in the corneal endothelial cell loss after pars plana and pars limbal insertion of the Baerveldt glaucoma implantEtsuo Chihara, Masaki Tanito, Michihiro Kono, et al.
The Journal of Dermatology|August 19, 2008
Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypesTaisuke Kondo, Tamio Suzuki, Yoshihiko Mitsuhashi, et al.
Journal of Dermatological Science|February 23, 2002
A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1)Eriko Nakamura, Yoshinori Miyamura, Jun Matsunaga, et al.
The American Journal of Dermatopathology|August 1, 2020
MYB Translocations in Both Myoepithelial and Ductoglandular Epithelial Cells in Adenoid Cystic Carcinoma: A Histopathologic and Genetic Reappraisal in Six Primary Cutaneous CasesKeisuke Goto, Kazuyoshi Kajimoto, Takashi Sugino, et al.
Journal of Dermatological Science|August 28, 2023
Eosinophil-derived galectin-10 upregulates matrix metalloproteinase expression in bullous pemphigoid blistersTakahiko Sato, Takahito Chiba, Takeshi Nakahara, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2Takayuki Konno, Yuko Abe, Masakazu Kawaguchi, et al.
Pageof 8