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Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
Zheng, Bixia; Seltzsam, Steve; Wang, Chunyan; Schierbaum, Luca; Schneider, Sophia; Wu, Chen-Han Wilfred; Dai, Rufeng; Connaughton, Dervla M; Nakayama, Makiko; Mann, Nina; Stajic, Natasa; Mane, Shrikant; Bauer, Stuart B; Tasic, Velibor; Nam, Hyun Joo; Shril, Shirlee; Hildebrandt, Friedhelm.
Afiliação
  • Zheng B; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Seltzsam S; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Wang C; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Schierbaum L; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Schneider S; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Wu CW; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Dai R; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Connaughton DM; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Nakayama M; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Mann N; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Stajic N; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Mane S; Department of Pediatric Nephrology, Institute for Mother and Child Health Care, Belgrade, Serbia.
  • Bauer SB; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Tasic V; Department of Urology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Nam HJ; Medical Faculty of Skopje, University Children's Hospital, Skopje, Macedonia.
  • Shril S; Department of Biological and Environmental Science, Texas A&M University at Commerce, Commerce, TX, USA.
  • Hildebrandt F; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Nephrol Dial Transplant ; 37(10): 1833-1843, 2022 09 22.
Article em En | MEDLINE | ID: mdl-34473308
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Urinário / Anormalidades Urogenitais Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido
Texto completo
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Urinário / Anormalidades Urogenitais Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido