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Deborah Tamura

Showing results (11-20 of 36) with videos related to

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Plos One|June 14, 2018
Four-dimensional, dynamic mosaicism is a hallmark of normal human skin that permits mapping of the organization and patterning of human epidermis during terminal differentiationYun Wang, Taro Masaki, Sikandar G Khan, et al.
Experimental Dermatology|May 26, 2022
Trichothiodystrophy hair shafts display distinct ultrastructural featuresAngeliki-Diotima Ioannidis, Sikandar G Khan, Deborah Tamura, et al.
Plos Genetics|December 2, 2024
Different germline variants in the XPA gene are associated with severe, intermediate, or mild neurodegeneration in xeroderma pigmentosum patientsJeffrey P Sagun, Sikandar G Khan, Kyoko Imoto, et al.
Obstetrics and Gynecology|September 11, 2019
Reproductive Health in Xeroderma Pigmentosum: Features of Premature AgingMelissa Merideth, Deborah Tamura, Divya Angra, et al.
Frontiers in Oncology|November 13, 2023
Retrospective study of efficacy and adverse events of immune checkpoint inhibitors in 22 xeroderma pigmentosum patients with metastatic or unresectable cancersElvelyn R Fernandez, Deborah Tamura, Sikandar G Khan, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosumXiaolong Zhou, Sikandar G Khan, Deborah Tamura, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 10, 2013
Histopathology of the inner ear in patients with xeroderma pigmentosum and neurologic degenerationLucas M Viana, Mohammad Seyyedi, Carmen C Brewer, et al.
Human Mutation|May 13, 2008
Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophyJennifer Boyle, Takahiro Ueda, Kyu-Seon Oh, et al.
The Journal of Investigative Dermatology|July 19, 2025
RNA Lariat-Debranching Enzyme (DBR1) Variations in Sabinas Brittle Hair Syndrome Form of Trichothiodystrophy: A Trichothiodystrophy-Causing GeneSikandar G Khan, Wenelia Baghoomian, Christiane Kuschal-Tauzon, et al.
Journal of the American Academy of Dermatology|October 2, 2017
Recurrent scarring papulovesicular lesions on sun-exposed skin in a 22-year-old manMelissa A Levoska, Jeffrey I Cohen, Irini Manoli, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Plos One|June 14, 2018
Four-dimensional, dynamic mosaicism is a hallmark of normal human skin that permits mapping of the organization and patterning of human epidermis during terminal differentiationYun Wang, Taro Masaki, Sikandar G Khan, et al.
Experimental Dermatology|May 26, 2022
Trichothiodystrophy hair shafts display distinct ultrastructural featuresAngeliki-Diotima Ioannidis, Sikandar G Khan, Deborah Tamura, et al.
Plos Genetics|December 2, 2024
Different germline variants in the XPA gene are associated with severe, intermediate, or mild neurodegeneration in xeroderma pigmentosum patientsJeffrey P Sagun, Sikandar G Khan, Kyoko Imoto, et al.
Obstetrics and Gynecology|September 11, 2019
Reproductive Health in Xeroderma Pigmentosum: Features of Premature AgingMelissa Merideth, Deborah Tamura, Divya Angra, et al.
Frontiers in Oncology|November 13, 2023
Retrospective study of efficacy and adverse events of immune checkpoint inhibitors in 22 xeroderma pigmentosum patients with metastatic or unresectable cancersElvelyn R Fernandez, Deborah Tamura, Sikandar G Khan, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosumXiaolong Zhou, Sikandar G Khan, Deborah Tamura, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 10, 2013
Histopathology of the inner ear in patients with xeroderma pigmentosum and neurologic degenerationLucas M Viana, Mohammad Seyyedi, Carmen C Brewer, et al.
Human Mutation|May 13, 2008
Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophyJennifer Boyle, Takahiro Ueda, Kyu-Seon Oh, et al.
The Journal of Investigative Dermatology|July 19, 2025
RNA Lariat-Debranching Enzyme (DBR1) Variations in Sabinas Brittle Hair Syndrome Form of Trichothiodystrophy: A Trichothiodystrophy-Causing GeneSikandar G Khan, Wenelia Baghoomian, Christiane Kuschal-Tauzon, et al.
Journal of the American Academy of Dermatology|October 2, 2017
Recurrent scarring papulovesicular lesions on sun-exposed skin in a 22-year-old manMelissa A Levoska, Jeffrey I Cohen, Irini Manoli, et al.
Pageof 4