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- [1] MBTPS2 Mutation Causes BRESEK/BRESHECK SyndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (01) : 97 - 102Naiki, Misako论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, Japan Nagoya Univ, Dept Pediat, Grad Sch Med, Nagoya, Aichi 4648601, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanMizuno, Seiji论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Dept Pediat, Cent Hosp, Kasugai, Aichi 4800392, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanYamada, Kenichiro论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanYamada, Yasukazu论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanKimura, Reiko论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanOshiro, Makoto论文数: 0 引用数: 0 h-index: 0机构: Japanese Red Cross Nagoya Daiichi Hosp, Dept Pediat, Nagoya, Aichi, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr, Dept Med Genet, Izumi, Osaka, Japan Res Inst Maternal & Child Hlth, Izumi, Osaka, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanMakita, Yoshio论文数: 0 引用数: 0 h-index: 0机构: Asahikawa Med Univ, Educ Ctr, Asahikawa, Hokkaido, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanSeishima, Mariko论文数: 0 引用数: 0 h-index: 0机构: Gifu Univ, Dept Dermatol, Grad Sch Med, Gifu, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, JapanWakamatsu, Nobuaki论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, Japan Aichi Human Serv Ctr, Dept Genet, Inst Dev Res, Kasugai, Aichi 4800392, Japan
- [2] MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaNATURE COMMUNICATIONS, 2016, 7Lindert, Uschi论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, Switzerland Univ Childrens Hosp Zurich, Childrens Res Ctr, CH-8032 Zurich, Switzerland Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandCabral, Wayne A.论文数: 0 引用数: 0 h-index: 0机构: NICHHD, Sect Heritable Disorders Bone & Extracellular Mat, NIH, Bethesda, MD 20892 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandAusavarat, Surasawadee论文数: 0 引用数: 0 h-index: 0机构: Chulalongkorn Univ, Fac Med, Ctr Excellence Med Genet, Dept Pediat, Bangkok 10330, Thailand Thai Red Cross Soc, King Chulalongkorn Mem Hosp, Excellence Ctr Med Genet, Bangkok 10330, Thailand Mahidol Univ, Siriraj Hosp, Fac Med, Dept Radiol,Div Nucl Med, Bangkok 10700, Thailand Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandTongkobpetch, Siraprapa论文数: 0 引用数: 0 h-index: 0机构: Chulalongkorn Univ, Fac Med, Ctr Excellence Med Genet, Dept Pediat, Bangkok 10330, Thailand Thai Red Cross Soc, King Chulalongkorn Mem Hosp, Excellence Ctr Med Genet, Bangkok 10330, Thailand Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandLudin, Katja论文数: 0 引用数: 0 h-index: 0机构: Kantonsspital Aarau, Dept Med Genet, Ctr Lab Med, CH-5001 Aarau, Switzerland Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandBarnes, Aileen M.论文数: 0 引用数: 0 h-index: 0机构: NICHHD, Sect Heritable Disorders Bone & Extracellular Mat, NIH, Bethesda, MD 20892 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, Switzerland论文数: 引用数: h-index:机构:Weis, Maryann论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Orthoped & Sports Med, Seattle, WA 98195 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandKrabichler, Birgit论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Div Human Genet, A-6020 Innsbruck, Austria Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandSrichomthong, Chalurmpon论文数: 0 引用数: 0 h-index: 0机构: Chulalongkorn Univ, Fac Med, Ctr Excellence Med Genet, Dept Pediat, Bangkok 10330, Thailand Thai Red Cross Soc, King Chulalongkorn Mem Hosp, Excellence Ctr Med Genet, Bangkok 10330, Thailand Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandMakareeva, Elena N.论文数: 0 引用数: 0 h-index: 0机构: NICHHD, Sect Phys Biochem, NIH, Bethesda, MD 20892 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandJanecke, Andreas R.论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Div Human Genet, A-6020 Innsbruck, Austria Med Univ Innsbruck, Dept Pediat 1, A-6020 Innsbruck, Austria Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandLeikin, Sergey论文数: 0 引用数: 0 h-index: 0机构: NICHHD, Sect Phys Biochem, NIH, Bethesda, MD 20892 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandRothlisberger, Benno论文数: 0 引用数: 0 h-index: 0机构: Kantonsspital Aarau, Dept Med Genet, Ctr Lab Med, CH-5001 Aarau, Switzerland Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandRohrbach, Marianne论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, Switzerland Univ Childrens Hosp Zurich, Childrens Res Ctr, CH-8032 Zurich, Switzerland Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandKennerknecht, Ingo论文数: 0 引用数: 0 h-index: 0机构: Univ Munster, Inst Human Genet, D-48149 Munster, Germany Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandEyre, David R.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Orthoped & Sports Med, Seattle, WA 98195 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandSuphapeetiporn, Kanya论文数: 0 引用数: 0 h-index: 0机构: Chulalongkorn Univ, Fac Med, Ctr Excellence Med Genet, Dept Pediat, Bangkok 10330, Thailand Thai Red Cross Soc, King Chulalongkorn Mem Hosp, Excellence Ctr Med Genet, Bangkok 10330, Thailand Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandGiunta, Cecilia论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, Switzerland Univ Childrens Hosp Zurich, Childrens Res Ctr, CH-8032 Zurich, Switzerland Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandMarini, Joan C.论文数: 0 引用数: 0 h-index: 0机构: NICHHD, Sect Heritable Disorders Bone & Extracellular Mat, NIH, Bethesda, MD 20892 USA Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, SwitzerlandShotelersuk, Vorasuk论文数: 0 引用数: 0 h-index: 0机构: Chulalongkorn Univ, Fac Med, Ctr Excellence Med Genet, Dept Pediat, Bangkok 10330, Thailand Thai Red Cross Soc, King Chulalongkorn Mem Hosp, Excellence Ctr Med Genet, Bangkok 10330, Thailand Univ Childrens Hosp Zurich, Div Metab, Connect Tissue Unit, CH-8032 Zurich, Switzerland
- [3] MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaNature Communications, 7Uschi Lindert论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismWayne A. Cabral论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismSurasawadee Ausavarat论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismSiraprapa Tongkobpetch论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismKatja Ludin论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismAileen M. Barnes论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismPatra Yeetong论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismMaryann Weis论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismBirgit Krabichler论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismChalurmpon Srichomthong论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismElena N. Makareeva论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismAndreas R. Janecke论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismSergey Leikin论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismBenno Röthlisberger论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismMarianne Rohrbach论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismIngo Kennerknecht论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismDavid R. Eyre论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismKanya Suphapeetiporn论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismCecilia Giunta论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismJoan C. Marini论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of MetabolismVorasuk Shotelersuk论文数: 0 引用数: 0 h-index: 0机构: Connective Tissue Unit and Children’s Research Center,Division of Metabolism
- [4] A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontiaINTERNATIONAL JOURNAL OF DERMATOLOGY, 2010, 49 (12) : 1399 - 1402论文数: 引用数: h-index:机构:Ur-Rehman, Fazal论文数: 0 引用数: 0 h-index: 0机构: Quaid I Azam Univ, Fac Biol Sci, Dept Microbiol, Islamabad, Pakistan Quaid I Azam Univ, Fac Biol Sci, Dept Biochem, Islamabad, PakistanYasinzai, Masoom论文数: 0 引用数: 0 h-index: 0机构: Univ Baluchistan, Inst Biochem, Quetta, Pakistan Quaid I Azam Univ, Fac Biol Sci, Dept Biochem, Islamabad, Pakistan论文数: 引用数: h-index:机构:
- [5] A Novel Mutation in the MBTPS2 Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia SyndromeANNALS OF DERMATOLOGY, 2022, 34 (01) : 59 - 62论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Kim, Moon-Bum论文数: 0 引用数: 0 h-index: 0机构: Pusan Natl Univ, Sch Med, Dept Dermatol, Busan, South Korea Pusan Natl Univ, Sch Med, Dept Dermatol, Busan, South Korea论文数: 引用数: h-index:机构:
- [6] A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndromeJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (05): : 1650 - 1653Maya-Nuñez, G论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguo Social, Ctr Med Nacl Siglo XXI, Hosp Pediat, Res Unit Dev Biol, Mexico City, DF, MexicoZenteno, JC论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguo Social, Ctr Med Nacl Siglo XXI, Hosp Pediat, Res Unit Dev Biol, Mexico City, DF, MexicoUlloa-Aguirre, A论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguo Social, Ctr Med Nacl Siglo XXI, Hosp Pediat, Res Unit Dev Biol, Mexico City, DF, MexicoKofman-Alfaro, S论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguo Social, Ctr Med Nacl Siglo XXI, Hosp Pediat, Res Unit Dev Biol, Mexico City, DF, MexicoMendez, JP论文数: 0 引用数: 0 h-index: 0机构: Inst Mexicano Seguo Social, Ctr Med Nacl Siglo XXI, Hosp Pediat, Res Unit Dev Biol, Mexico City, DF, Mexico
- [7] Recurrent splice-site mutation in MBTPS2 underlying IFAP syndrome with Olmsted syndrome-like features in a Chinese patientCLINICAL AND EXPERIMENTAL DERMATOLOGY, 2014, 39 (02) : 158 - 161Wang, H. J.论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R China Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R ChinaTang, Z. L.论文数: 0 引用数: 0 h-index: 0机构: Qingdao Univ, Coll Med, Affiliated Hosp, Dept Dermatol, Qingdao 266071, Peoples R China Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R ChinaLin, Z. M.论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R China Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R ChinaDai, L. L.论文数: 0 引用数: 0 h-index: 0机构: BGI Shenzhen, Shenzhen, Peoples R China Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R ChinaChen, Q.论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R China Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R ChinaYang, Y.论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R China Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China Peking Univ, Hosp 1, Dept Dermatol, Beijing 100034, Peoples R China
- [8] A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutationJournal of Human Genetics, 2011, 56 : 250 - 252Junko Nakayama论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsNobuaki Iwasaki论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsKenji Shin论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsHideo Sato论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsMariko Kamo论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsManabu Ohyama论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsEmiko Noguchi论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of PediatricsTadao Arinami论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural University of Health Sciences,Department of Pediatrics
- [9] A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutationJOURNAL OF HUMAN GENETICS, 2011, 56 (03) : 250 - 252Nakayama, Junko论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural Univ Hlth Sci, Dept Pediat, Ibaraki, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanIwasaki, Nobuaki论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural Univ Hlth Sci, Dept Pediat, Ibaraki, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanShin, Kenji论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural Univ Hlth Sci, Dept Pediat, Ibaraki, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanSato, Hideo论文数: 0 引用数: 0 h-index: 0机构: Ibaraki Prefectural Univ Hlth Sci, Dept Pediat, Ibaraki, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanKamo, Mariko论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Dept Dermatol, Tokyo, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanOhyama, Manabu论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Dept Dermatol, Tokyo, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanNoguchi, Emiko论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, JapanArinami, Tadao论文数: 0 引用数: 0 h-index: 0机构: Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, Japan Univ Tsukuba, Dept Med Genet, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058577, Japan
- [10] A novel mutation in MBTPS2 causes ichthyosis follicularis, alopecia, and photophobia syndromeMOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (08):Jiang, Yanyun论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Dermatol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Peking Union Med Coll, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Dermatol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaJin, Hongzhong论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Dermatol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Peking Union Med Coll, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Dermatol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R ChinaZeng, Yueping论文数: 0 引用数: 0 h-index: 0机构: Chinese Acad Med Sci, Dept Dermatol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China Peking Union Med Coll, Beijing 100730, Peoples R China Chinese Acad Med Sci, Dept Dermatol, Peking Union Med Coll Hosp, Beijing 100730, Peoples R China