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Updated: May 12, 2026

A Quantitative Cell Migration Assay for Murine Enteric Neural Progenitors
08:26

A Quantitative Cell Migration Assay for Murine Enteric Neural Progenitors

Published on: September 18, 2013

RET増強剤における一般的な性依存変異が,ヒルシュプリング病のリスクの基礎となっている

Eileen Sproat Emison1, Andrew S McCallion, Carl S Kashuk

  • 1McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

Nature
|April 15, 2005
PubMed
まとめ

RET遺伝子の一般的な遺伝的変異は,ヒルシュプリング病 (HSCR) のリスクを大幅に増加させます. この低浸透性の変種は,エンハンサー領域で見つかっており,このまれな疾患の複雑な遺伝パターンを説明します.

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Diagnosis of Hirschsprung's Disease by Immunostaining Rectal Suction Biopsies for Calretinin, S100 Protein and Protein Gene Product 9.505:45

Diagnosis of Hirschsprung's Disease by Immunostaining Rectal Suction Biopsies for Calretinin, S100 Protein and Protein Gene Product 9.5

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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information09:37

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

Published on: August 15, 2019

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