BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

307 related articles for article (PubMed ID: 10790203)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. Mutational analysis of RET/GDNF/NTN genes in children with total colonic aganglionosis with small bowel involvement.
    Inoue K; Shimotake T; Iwai N
    Am J Med Genet; 2000 Aug; 93(4):278-84. PubMed ID: 10946353
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
    Attié T; Pelet A; Edery P; Eng C; Mulligan LM; Amiel J; Boutrand L; Beldjord C; Nihoul-Fékété C; Munnich A
    Hum Mol Genet; 1995 Aug; 4(8):1381-6. PubMed ID: 7581377
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease.
    Doray B; Salomon R; Amiel J; Pelet A; Touraine R; Billaud M; Attié T; Bachy B; Munnich A; Lyonnet S
    Hum Mol Genet; 1998 Sep; 7(9):1449-52. PubMed ID: 9700200
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease.
    Carlomagno F; Melillo RM; Visconti R; Salvatore G; De Vita G; Lupoli G; Yu Y; Jing S; Vecchio G; Fusco A; Santoro M
    Endocrinology; 1998 Aug; 139(8):3613-9. PubMed ID: 9681515
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
    Woodward ER; Eng C; McMahon R; Voutilainen R; Affara NA; Ponder BA; Maher ER
    Hum Mol Genet; 1997 Jul; 6(7):1051-6. PubMed ID: 9215674
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hirschsprung associated GDNF mutations do not prevent RET activation.
    Borghini S; Bocciardi R; Bonardi G; Matera I; Santamaria G; Ravazzolo R; Ceccherini I
    Eur J Hum Genet; 2002 Mar; 10(3):183-7. PubMed ID: 11973622
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease.
    Borrego S; Eng C; Sánchez B; Sáez ME; Navarro E; Antiñolo G
    J Clin Endocrinol Metab; 1998 Sep; 83(9):3361-4. PubMed ID: 9745455
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Functional characterization of mutations in the GDNF gene of patients with Hirschsprung disease.
    Eketjäll S; Ibáñez CF
    Hum Mol Genet; 2002 Feb; 11(3):325-9. PubMed ID: 11823451
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
    Angrist M; Bolk S; Thiel B; Puffenberger EG; Hofstra RM; Buys CH; Cass DT; Chakravarti A
    Hum Mol Genet; 1995 May; 4(5):821-30. PubMed ID: 7633441
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.
    Geneste O; Bidaud C; De Vita G; Hofstra RM; Tartare-Deckert S; Buys CH; Lenoir GM; Santoro M; Billaud M
    Hum Mol Genet; 1999 Oct; 8(11):1989-99. PubMed ID: 10484767
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.