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T Takeichi

Showing results (61-70 of 69) with videos related to

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The British Journal of Dermatology|July 26, 2014
Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in KuwaitT Takeichi, A Nanda, L Liu, et al.
The British Journal of Dermatology|July 14, 2016
Syndromic inherited poikiloderma due to a de novo mutation in FAM111BT Takeichi, A Nanda, H-S Yang, et al.
Clinical and Experimental Dermatology|July 17, 2015
Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLGA Cuell, N Bansal, T Cole, et al.
Transplantation|February 24, 2001
Living-related liver transplantation for type II citrullinemia using a graft from heterozygote donorM Kasahara, S Ohwada, T Takeichi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 3, 2021
Intravenous allogeneic multilineage-differentiating stress-enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open-label studyY Fujita, T Nohara, S Takashima, et al.
The British Journal of Dermatology|January 26, 2018
Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school childrenM Kono, M Akiyama, Y Inoue, et al.
Transplantation Proceedings|March 20, 1999
Effects of fatty infiltration of the graft on the outcome of living-related liver transplantationM Hayashi, K Fujii, T Kiuchi, et al.
The British Journal of Dermatology|June 21, 2014
Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratoryT Takeichi, L Liu, K Fong, et al.
The British Journal of Dermatology|September 20, 2014
Progressive hyperpigmentation in a Taiwanese child due to an inborn error of vitamin B12 metabolism (cblJ)T Takeichi, C-K Hsu, H-S Yang, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
The British Journal of Dermatology|July 26, 2014
Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in KuwaitT Takeichi, A Nanda, L Liu, et al.
The British Journal of Dermatology|July 14, 2016
Syndromic inherited poikiloderma due to a de novo mutation in FAM111BT Takeichi, A Nanda, H-S Yang, et al.
Clinical and Experimental Dermatology|July 17, 2015
Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLGA Cuell, N Bansal, T Cole, et al.
Transplantation|February 24, 2001
Living-related liver transplantation for type II citrullinemia using a graft from heterozygote donorM Kasahara, S Ohwada, T Takeichi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 3, 2021
Intravenous allogeneic multilineage-differentiating stress-enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open-label studyY Fujita, T Nohara, S Takashima, et al.
The British Journal of Dermatology|January 26, 2018
Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school childrenM Kono, M Akiyama, Y Inoue, et al.
Transplantation Proceedings|March 20, 1999
Effects of fatty infiltration of the graft on the outcome of living-related liver transplantationM Hayashi, K Fujii, T Kiuchi, et al.
The British Journal of Dermatology|June 21, 2014
Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratoryT Takeichi, L Liu, K Fong, et al.
The British Journal of Dermatology|September 20, 2014
Progressive hyperpigmentation in a Taiwanese child due to an inborn error of vitamin B12 metabolism (cblJ)T Takeichi, C-K Hsu, H-S Yang, et al.
Pageof 7