Literature DB >> 7997019

De-novo mutations of the RET proto-oncogene in Hirschsprung's disease.

A Pelet, T Attie, O Goulet, C Eng, B A Ponder, A Munnich, S Lyonnet.   

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Year:  1994        PMID： 7997019     DOI： 10.1016/s0140-6736(94)92908-4

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  6 in total

Review 1.  Hirschsprung's disease as a neurochristopathy.

Authors:  G Martucciello
Journal:  Pediatr Surg Int       Date:  1997       Impact factor: 1.827

2.  The development of colon innervation in trisomy 16 mice and Hirschsprung's disease.

Authors:  J C Li; K H Mi; J L Zhou; L Busch; W Kuhnel
Journal:  World J Gastroenterol       Date:  2001-02       Impact factor: 5.742

3.  Oncological implications of RET gene mutations in Hirschsprung's disease.

Authors:  R H Sijmons; R M Hofstra; F A Wijburg; T P Links; R P Zwierstra; A Vermey; D C Aronson; G Tan-Sindhunata; G J Brouwers-Smalbraak; S M Maas; C H Buys
Journal:  Gut       Date:  1998-10       Impact factor: 23.059

Review 4.  Hirschsprung's disease: clinical dysmorphology, genes, micro-RNAs, and future perspectives.

Authors:  Consolato Maria Sergi; Oana Caluseriu; Hunter McColl; David D Eisenstat
Journal:  Pediatr Res       Date:  2016-09-28       Impact factor: 3.756

5.  Renal aplasia in humans is associated with RET mutations.

Authors:  Michael A Skinner; Shawn D Safford; Justin G Reeves; Margaret E Jackson; Alex J Freemerman
Journal:  Am J Hum Genet       Date:  2008-01-31       Impact factor: 11.025

Review 6.  The RET gene encodes RET protein, which triggers intracellular signaling pathways for enteric neurogenesis, and RET mutation results in Hirschsprung's disease.

Authors:  Chacchu Bhattarai; Phanindra Prasad Poudel; Arnab Ghosh; Sneha Guruprasad Kalthur
Journal:  AIMS Neurosci       Date:  2022-03-16
  6 in total

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