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The Journal of Dermatology|October 29, 2015
Postoperative gluteal skin damage associated with latent development of gluteal muscle damageYukari Hattori, Takashi Ikeuchi, Yoshihiro Kuroda, et al.Proceedings of the National Academy of Sciences of the United States of America|June 26, 2023
Deep intronic founder mutations identified in the ERCC4/XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosumChikako Senju, Yuka Nakazawa, Taichi Oso, et al.The Journal of Dermatology|January 12, 2022
Clinical practice guidelines for pseudoxanthoma elasticum (2017): Clinical Practice Guidelines for Pseudoxanthoma Elasticum Drafting CommitteeAkira Iwanaga, Atsushi Utani, Yuta Koike, et al.Blood|October 2, 2004
Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndromeNobuo Kanazawa, Ikuo Okafuji, Naotomo Kambe, et al.The Journal of Dermatology|February 11, 2017
Analysis of clinical symptoms and ABCC6 mutations in 76 Japanese patients with pseudoxanthoma elasticumAkira Iwanaga, Yumi Okubo, Mariko Yozaki, et al.Nature Genetics|April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repairYuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.American Journal of Human Genetics|April 30, 2013
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaKazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, et al.Pageof 6