These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 9760196)

  • 1. Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B).
    Svensson PJ; Anvret M; Molander ML; Nordenskjöld A
    Hum Genet; 1998 Aug; 103(2):145-8. PubMed ID: 9760196
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Japanese patients with sporadic Hirschsprung: mutation analysis of the receptor tyrosine kinase proto-oncogene, endothelin-B receptor, endothelin-3, glial cell line-derived neurotrophic factor and neurturin genes: a comparison with similar studies.
    Sakai T; Nirasawa Y; Itoh Y; Wakizaka A
    Eur J Pediatr; 2000 Mar; 159(3):160-7. PubMed ID: 10664228
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.
    Gath R; Goessling A; Keller KM; Koletzko S; Coerdt W; Müntefering H; Wirth S; Hofstra RM; Mulligan L; Eng C; von Deimling A
    Gut; 2001 May; 48(5):671-5. PubMed ID: 11302967
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Molecular basis of Hirschsprung disease].
    Inoue M; Okada A
    Nihon Rinsho; 1998 Jan; 56(1):249-57. PubMed ID: 9465697
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital central hypoventilation syndrome: a novel mutation of the RET gene in an isolated case.
    Kanai M; Numakura C; Sasaki A; Shirahata E; Akaba K; Hashimoto M; Hasegawa H; Shirasawa S; Hayasaka K
    Tohoku J Exp Med; 2002 Apr; 196(4):241-6. PubMed ID: 12086152
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
    Angrist M; Bolk S; Halushka M; Lapchak PA; Chakravarti A
    Nat Genet; 1996 Nov; 14(3):341-4. PubMed ID: 8896568
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From monogenic to polygenic: model of Hirschsprung disease].
    Salomon R; Amiel J; Attié T; Pelet A; Munnich A; Lyonnet S
    Pathol Biol (Paris); 1998 Nov; 46(9):705-7. PubMed ID: 9885824
    [TBL] [Abstract][Full Text] [Related]  

  • 8. RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems.
    Hofstra RM; Wu Y; Stulp RP; Elfferich P; Osinga J; Maas SM; Siderius L; Brooks AS; vd Ende JJ; Heydendael VM; Severijnen RS; Bax KM; Meijers C; Buys CH
    Hum Mutat; 2000; 15(5):418-29. PubMed ID: 10790203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Point nucleotidic changes in both the RET proto-oncogene and the endothelin-B receptor gene in a Hirschsprung disease patient associated with Down syndrome.
    Sakai T; Wakizaka A; Nirasawa Y; Ito Y
    Tohoku J Exp Med; 1999 Jan; 187(1):43-7. PubMed ID: 10458491
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.
    Garcia-Barceló M; Sham MH; Lee WS; Lui VC; Chen BL; Wong KK; Wong JS; Tam PK
    Clin Chem; 2004 Jan; 50(1):93-100. PubMed ID: 14633923
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb.
    McCallion AS; Stames E; Conlon RA; Chakravarti A
    Proc Natl Acad Sci U S A; 2003 Feb; 100(4):1826-31. PubMed ID: 12574515
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
    Salomon R; Attié T; Pelet A; Bidaud C; Eng C; Amiel J; Sarnacki S; Goulet O; Ricour C; Nihoul-Fékété C; Munnich A; Lyonnet S
    Nat Genet; 1996 Nov; 14(3):345-7. PubMed ID: 8896569
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.
    Munnes M; Fanaei S; Schmitz B; Muiznieks I; Holschneider AM; Doerfler W
    Am J Med Genet; 2000 Sep; 94(1):19-27. PubMed ID: 10982477
    [TBL] [Abstract][Full Text] [Related]  

  • 14. RET proto-oncogene: role in kidney development and molecular pathology.
    Salomon R; Attie T; Amiel J; Pelet A; Niaudet P; Lyonnet S
    Adv Nephrol Necker Hosp; 1998; 28():401-17. PubMed ID: 9890001
    [No Abstract]   [Full Text] [Related]  

  • 15. Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.
    Carrasquillo MM; McCallion AS; Puffenberger EG; Kashuk CS; Nouri N; Chakravarti A
    Nat Genet; 2002 Oct; 32(2):237-44. PubMed ID: 12355085
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease.
    Vanhorne JB; Gimm O; Myers SM; Kaushik A; von Deimling A; Eng C; Mulligan LM
    Hum Genet; 2001 May; 108(5):409-15. PubMed ID: 11409869
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Double heterozygosity for a RET substitution interfering with splicing and an EDNRB missense mutation in Hirschsprung disease.
    Auricchio A; Griseri P; Carpentieri ML; Betsos N; Staiano A; Tozzi A; Priolo M; Thompson H; Bocciardi R; Romeo G; Ballabio A; Ceccherini I
    Am J Hum Genet; 1999 Apr; 64(4):1216-21. PubMed ID: 10090908
    [No Abstract]   [Full Text] [Related]  

  • 18. Low frequency of RET mutations in Hirschsprung disease in Sweden.
    Svensson PJ; Molander ML; Eng C; Anvret M; Nordenskjöld A
    Clin Genet; 1998 Jul; 54(1):39-44. PubMed ID: 9727738
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
    Ivanchuk SM; Myers SM; Eng C; Mulligan LM
    Hum Mol Genet; 1996 Dec; 5(12):2023-6. PubMed ID: 8968758
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetics of Hirschsprung disease].
    Attié T; Amiel J; Jan D; Edery P; Pelet A; Salomon R; Munnich A; Lyonnet S; Nihoul-Fékété C
    Ann Chir; 1996; 50(7):538-41. PubMed ID: 9035423
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.