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T Takeichi

Showing results (31-40 of 69) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|March 28, 2012
Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthoodK Tanahashi, K Sugiura, T Takeichi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 24, 2017
Trichothiodystrophy, complementation group A complicated with squamous cell carcinomaT Takeichi, S Tomimura, Y Okuno, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 4, 2020
A patient with CARD14-associated papulosquamous eruptions showing atopic dermatitis-like featuresT Takeichi, S Terawaki, Y Kubota, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 22, 2007
Whole-liver graft without the retrohepatic inferior vena cava for sequential (domino) living donor liver transplantationY Inomata, M E Zeledón, K Asonuma, et al.
The British Journal of Dermatology|April 1, 2018
Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expressionM Kono, M Suganuma, A Dutta, et al.
Clinical and Experimental Dermatology|February 17, 2015
Ichthyosis follicularis, atrichia, and photophobia syndrome associated with a new mutation in MBTPS2K Fong, T Takeichi, L Liu, et al.
The British Journal of Dermatology|July 14, 2019
A patient with bullous pemphigoid with mucosal involvement serologically positive for anti-BP230 autoantibodies onlyT Taki, T Takeichi, M Kono, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|November 1, 1989
[Hyperimmunoglobulinemia E syndrome with deformity of bilateral fingers, juvenile cataracta and impairment of neutrophil phagocytosis]T Takeichi, T Naruo, J Itoh, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 19, 2018
Dyschromatosis symmetrica hereditaria with chilblains due to a novel two-amino-acid deletion in the double-stranded RNA-binding domain of ADAR1M Kono, M Suganuma, T Shimada, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 12, 2016
Punctate palmoplantar keratoderma type 1 with a novel AAGAB frameshift mutation: intrafamilial phenotype variation due to ageingM Kono, K Fukai, N Shimizu, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
Journal of the European Academy of Dermatology and Venereology : JEADV|March 28, 2012
Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthoodK Tanahashi, K Sugiura, T Takeichi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 24, 2017
Trichothiodystrophy, complementation group A complicated with squamous cell carcinomaT Takeichi, S Tomimura, Y Okuno, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 4, 2020
A patient with CARD14-associated papulosquamous eruptions showing atopic dermatitis-like featuresT Takeichi, S Terawaki, Y Kubota, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 22, 2007
Whole-liver graft without the retrohepatic inferior vena cava for sequential (domino) living donor liver transplantationY Inomata, M E Zeledón, K Asonuma, et al.
The British Journal of Dermatology|April 1, 2018
Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expressionM Kono, M Suganuma, A Dutta, et al.
Clinical and Experimental Dermatology|February 17, 2015
Ichthyosis follicularis, atrichia, and photophobia syndrome associated with a new mutation in MBTPS2K Fong, T Takeichi, L Liu, et al.
The British Journal of Dermatology|July 14, 2019
A patient with bullous pemphigoid with mucosal involvement serologically positive for anti-BP230 autoantibodies onlyT Taki, T Takeichi, M Kono, et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine|November 1, 1989
[Hyperimmunoglobulinemia E syndrome with deformity of bilateral fingers, juvenile cataracta and impairment of neutrophil phagocytosis]T Takeichi, T Naruo, J Itoh, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 19, 2018
Dyschromatosis symmetrica hereditaria with chilblains due to a novel two-amino-acid deletion in the double-stranded RNA-binding domain of ADAR1M Kono, M Suganuma, T Shimada, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 12, 2016
Punctate palmoplantar keratoderma type 1 with a novel AAGAB frameshift mutation: intrafamilial phenotype variation due to ageingM Kono, K Fukai, N Shimizu, et al.
Pageof 7