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Deborah Tamura

Showing results (1-10 of 36) with videos related to

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The Journal of Investigative Dermatology|May 14, 2010
Founder mutations in xeroderma pigmentosumDeborah Tamura, John J DiGiovanna, Kenneth H Kraemer
Photodermatology, Photoimmunology & Photomedicine|January 15, 2014
Living with xeroderma pigmentosum: comprehensive photoprotection for highly photosensitive patientsDeborah Tamura, John J DiGiovanna, Sikandar G Khan, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 12, 2014
Growth and nutrition in children with trichothiodystrophyEmily C Atkinson, Diana Thiara, Deborah Tamura, et al.
Photochemistry and Photobiology|March 11, 2011
Nucleotide excision repair proteins rapidly accumulate but fail to persist in human XP-E (DDB2 mutant) cellsKyu-Seon Oh, Kyoko Imoto, Steffen Emmert, et al.
The Journal of Investigative Dermatology|October 8, 2014
Mutations in the TTDN1 gene are associated with a distinct trichothiodystrophy phenotypeElizabeth R Heller, Sikandar G Khan, Christiane Kuschal, et al.
Pediatric Dermatology|June 9, 2021
Cockayne syndrome, MEN1, and genomic variants: Exome sequencing is changing our view of the genetic landscapeSandra R Oska, Deborah Tamura, Jenny E Blau, et al.
The Journal of Investigative Dermatology|January 13, 2021
Xeroderma Pigmentosum: A Model for Human Premature AgingElizabeth R H Rizza, John J DiGiovanna, Sikandar G Khan, et al.
Pediatrics|October 1, 2021
Metronidazole-Induced Hepatitis in a Teenager With Xeroderma Pigmentosum and Trichothiodystrophy OverlapAdesoji Abiona, Nuno Cordeiro, Heather Fawcett, et al.
Survey of Ophthalmology|June 21, 2011
Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literatureHema L Ramkumar, Brian P Brooks, Xiaoguang Cao, et al.
JAMA Dermatology|December 6, 2018
Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US PopulationJennifer Pugh, Sikandar G Khan, Deborah Tamura, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
The Journal of Investigative Dermatology|May 14, 2010
Founder mutations in xeroderma pigmentosumDeborah Tamura, John J DiGiovanna, Kenneth H Kraemer
Photodermatology, Photoimmunology & Photomedicine|January 15, 2014
Living with xeroderma pigmentosum: comprehensive photoprotection for highly photosensitive patientsDeborah Tamura, John J DiGiovanna, Sikandar G Khan, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 12, 2014
Growth and nutrition in children with trichothiodystrophyEmily C Atkinson, Diana Thiara, Deborah Tamura, et al.
Photochemistry and Photobiology|March 11, 2011
Nucleotide excision repair proteins rapidly accumulate but fail to persist in human XP-E (DDB2 mutant) cellsKyu-Seon Oh, Kyoko Imoto, Steffen Emmert, et al.
The Journal of Investigative Dermatology|October 8, 2014
Mutations in the TTDN1 gene are associated with a distinct trichothiodystrophy phenotypeElizabeth R Heller, Sikandar G Khan, Christiane Kuschal, et al.
Pediatric Dermatology|June 9, 2021
Cockayne syndrome, MEN1, and genomic variants: Exome sequencing is changing our view of the genetic landscapeSandra R Oska, Deborah Tamura, Jenny E Blau, et al.
The Journal of Investigative Dermatology|January 13, 2021
Xeroderma Pigmentosum: A Model for Human Premature AgingElizabeth R H Rizza, John J DiGiovanna, Sikandar G Khan, et al.
Pediatrics|October 1, 2021
Metronidazole-Induced Hepatitis in a Teenager With Xeroderma Pigmentosum and Trichothiodystrophy OverlapAdesoji Abiona, Nuno Cordeiro, Heather Fawcett, et al.
Survey of Ophthalmology|June 21, 2011
Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literatureHema L Ramkumar, Brian P Brooks, Xiaoguang Cao, et al.
JAMA Dermatology|December 6, 2018
Use of Big Data to Estimate Prevalence of Defective DNA Repair Variants in the US PopulationJennifer Pugh, Sikandar G Khan, Deborah Tamura, et al.
Pageof 4