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J-GLOBAL ID：201802251284409887 整理番号：18A1103827

TRPV6変異体は胎盤を通して母体胎児カルシウム輸送に干渉し,一過性新生児副甲状腺機能亢進症を引き起こす【JST・京大機械翻訳】

TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism

著者 (22件)：

Suzuki Yoshiro

(Division of Cell Signaling, Okazaki Institute for Integrative Bioscience (National Institute for Physiological Sciences), National Institutes of Natural Sciences, Okazaki 444-8787, Japan)

Suzuki Yoshiro

(Department of Physiological Sciences, SOKENDAI (The Graduate University for Advanced Studies), Okazaki 444-8787, Japan)

Chitayat David

(The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON M5G 1Z5, Canada)

Chitayat David

(Division of Clinical Genetics and Metabolism, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON M5G 1X8, Canada)

Sawada Hirotake

(Division of Pediatrics, Department of Developmental and Urological-Reproductive Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki 889-1692, Japan)

Deardorff Matthew A.

(Division of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA)

McLaughlin Heather M.

(GeneDx, Gaithersburg, MD 20877, USA)

Begtrup Amber

(GeneDx, Gaithersburg, MD 20877, USA)

Millar Kathryn

(The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON M5G 1Z5, Canada)

Harrington Jennifer

(Division of Endocrinology and Metabolism, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON M5G 1X8, Canada)

Chong Karen

(The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON M5G 1Z5, Canada)

Roifman Maian

(The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON M5G 1Z5, Canada)

Grand Katheryn

(Division of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA)

Tominaga Makoto

(Division of Cell Signaling, Okazaki Institute for Integrative Bioscience (National Institute for Physiological Sciences), National Institutes of Natural Sciences, Okazaki 444-8787, Japan)

Tominaga Makoto

(Department of Physiological Sciences, SOKENDAI (The Graduate University for Advanced Studies), Okazaki 444-8787, Japan)

Takada Fumio

(Department of Medical Genetics and Genomics, Graduate School of Medical Sciences, Kitasato University, Kanagawa 252-0375, Japan)

Takada Fumio

(Division of Genetics and Genomics, Center for Clinical Genetics and Genomics, Kitasato University Hospital, Kanagawa 252-0374, Japan)

Shuster Shirley

(The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, ON M5G 1Z5, Canada)

Obara Megumi

(Division of Pediatrics, Department of Developmental and Urological-Reproductive Medicine, Faculty of Medicine, University of Miyazaki, Miyazaki 889-1692, Japan)

Mutoh Hiroshi

(Department of Neonatology, Tokyo Metropolitan Children’s Medical Center, Tokyo 183-8561, Japan)

Kushima Reiko

(Department of Neonatology, Tokyo Metropolitan Bokutoh Hospital, Tokyo 130-8575, Japan)

Nishimura Gen

(Intractable Disease Center, Saitama Medical University Hospital, Saitama 350-1298, Japan)

資料名：

American Journal of Human Genetics (American Journal of Human Genetics)

巻： 102 号： 6 ページ： 1104-1114 発行年： 2018年
JST資料番号： B0360B ISSN： 0002-9297 資料種別：逐次刊行物 (A)
記事区分：原著論文発行国：オランダ (NLD) 言語：英語 (EN)

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