Molecular Basis of Hereditary Hair Diseases von Shimomura, Yutaka

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Journey toward unraveling the molecular basis of hereditary hair disorders von Shimomura, Yutaka, Ph.D

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Update of recent findings in genetic hair disorders von Hayashi, Ryota, Shimomura, Yutaka

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Congenital hair loss disorders: Rare, but not too rare von SHIMOMURA, Yutaka

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Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia von Asano, Nobuyuki, Yasuno, Shuichiro, Hayashi, Ryota, Shimomura, Yutaka

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Functional studies for a dominant mutation in the EDAR gene responsible for hypohidrotic ectodermal dysplasia von Okita, Tomoko, Asano, Nobuyuki, Yasuno, Shuichiro, Shimomura, Yutaka

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A homozygous loss‐of‐function variant in the MPO gene is associated with generalized pustular psoriasis von Onitsuka, Mami, Farooq, Muhammad, Iqbal, Muhammad Nasir, Yasuno, Shuichiro, Shimomura, Yutaka

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Genome-wide association study in alopecia areata implicates both innate and adaptive immunity von Christiano, Angela M, Petukhova, Lynn, Duvic, Madeleine, Hordinsky, Maria, Norris, David, Price, Vera, Shimomura, Yutaka, Kim, Hyunmi, Singh, Pallavi, Lee, Annette, Chen, Wei V, Meyer, Katja C, Paus, Ralf, Jahoda, Colin A. B, Amos, Christopher I, Gregersen, Peter K

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Two cases of severe congenital hypotrichosis caused by compound heterozygous mutations in the LSS gene von Murata, Mami, Hayashi, Ryota, Kawakami, Yoshio, Morizane, Shin, Shimomura, Yutaka

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Evidence for a dominant‐negative effect of a missense mutation in the SERPING1 gene responsible for hereditary angioedema type I von Yasuno, Shuichiro, Ansai, Osamu, Hayashi, Ryota, Nakamura, Sawako, Shimomura, Yutaka

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Different degree of loss‐of‐function among four missense mutations in the EDAR gene responsible for autosomal recessive hypohidrotic ectodermal dysplasia may be associated with the... von Yagi, Sasagu, Yasuno, Shuichiro, Ansai, Osamu, Hayashi, Ryota, Shimomura, Yutaka

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Guidelines for the diagnosis and treatment of male‐pattern and female‐pattern hair loss, 2017 version von Manabe, Motomu, Tsuboi, Ryoji, Itami, Satoshi, Osada, Shin‐Ichi, Amoh, Yasuyuki, Ito, Taisuke, Inui, Shigeki, Ueki, Rie, Ohyama, Manabu, Kurata, Sotaro, Kono, Takeshi, Saito, Norimitsu, Sato, Akio, Shimomura, Yutaka, Nakamura, Motonobu, Narusawa, Hiroshi, Yamazaki, Masashi

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APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex von Shimomura, Yutaka, Agalliu, Dritan, Vonica, Alin, Luria, Victor, Wajid, Muhammad, Baumer, Alessandra, Belli, Serena, Petukhova, Lynn, Schinzel, Albert, Brivanlou, Ali H., Barres, Ben A., Christiano, Angela M.

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Only plantar lesion of punctate palmoplantar keratoderma with a novel missense mutation in the AAGAB gene: Two Japanese familial case reports and review of reported mutations von Hasegawa, Akito, Hayashi, Ryota, Shimomura, Yutaka, Hirashima, Masanori, Abe, Riichiro

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Biology and genetics of hair von Shimomura, Yutaka, Christiano, Angela M

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A case of multiple oral cancers in the patient with hypohidrotic ectodermal dysplasia von Kobayashi, Takanori, Iida, Akihiko, Narimatsu, Kaya, Shimomura, Yutaka

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Expression studies of nectin-1 in human hair follicles and identification of a p63-responsive element in the NECTIN1 promoter von Hayashi, Ryota, M.D, Abe, Riichiro, M.D., Ph.D, Shimomura, Yutaka, M.D., Ph.D

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Hereditary angio-oedema with normal C1-INH, developing recurrent acute abdomen after taking low-dose oestrogen–progestin: A case report von Nakayama, Tsuyoshi, Tamimoto, Yasuhiro, Shimomura, Yutaka, Tsukamoto, Hiroshi

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Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family von Fujikawa, Hiroki, Fujimoto, Atsushi, Farooq, Muhammad, Ito, Masaaki, Shimomura, Yutaka

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First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24 von Hayashi, Ryota, Yoshida, Kazue, Abe, Riichiro, Niizeki, Hironori, Shimomura, Yutaka, M.D., Ph.D

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