Yoshito Takahashi

Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair

Yuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake et al. · Nature Genetics · 2012 · 210 citations · Full text

Genome Instability, Genetic Disorder, Medicine +6

Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia

Kazuya Kashiyama, Yuka Nakazawa, Daniela T. Pilz et al. · The American Journal of Human Genetics · 2013 · 203 citations · Full text

Fanconi Anemia, Genetics, Hematology +5

Rhododendrol, a depigmentation‐inducing phenolic compound, exerts melanocyte cytotoxicity via a tyrosinase‐dependent mechanism

Minoru Sasaki, Masatoshi Kondo, Kohji Sato et al. · Pigment Cell & Melanoma Research · 2014 · 123 citations · Full text

Hyaluronan Synthase 3 Regulates Hyaluronan Synthesis in Cultured Human Keratinocytes

Tetsuya Sayo, Yoshinori Sugiyama, Yoshito Takahashi et al. · Journal of Investigative Dermatology · 2002 · 115 citations · Full text

Regenerative Medicine, Medicine, Cutaneous Biology +7

Regulation of Hyaluronan (HA) Metabolism Mediated by HYBID (Hyaluronan-binding Protein Involved in HA Depolymerization, KIAA1199) and HA Synthases in Growth Factor-stimulated Fibroblasts

Aya Nagaoka, Hiroyuki Yoshida, Sachiko Nakamura et al. · Journal of Biological Chemistry · 2015 · 96 citations · Full text