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 *

125 related articles for article (PubMed ID: 23756430)

  • 1. The NF1 gene: a frequent mutational target in sporadic pheochromocytomas and beyond.
    Welander J; Söderkvist P; Gimm O
    Endocr Relat Cancer; 2013 Aug; 20(4):C13-7. PubMed ID: 23756430
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.
    Bausch B; Borozdin W; Mautner VF; Hoffmann MM; Boehm D; Robledo M; Cascon A; Harenberg T; Schiavi F; Pawlu C; Peczkowska M; Letizia C; Calvieri S; Arnaldi G; Klingenberg-Noftz RD; Reisch N; Fassina A; Brunaud L; Walter MA; Mannelli M; MacGregor G; Palazzo FF; Barontini M; Walz MK; Kremens B; Brabant G; Pfäffle R; Koschker AC; Lohoefner F; Mohaupt M; Gimm O; Jarzab B; McWhinney SR; Opocher G; Januszewicz A; Kohlhase J; Eng C; Neumann HP;
    J Clin Endocrinol Metab; 2007 Jul; 92(7):2784-92. PubMed ID: 17426081
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas.
    Welander J; Larsson C; Bäckdahl M; Hareni N; Sivlér T; Brauckhoff M; Söderkvist P; Gimm O
    Hum Mol Genet; 2012 Dec; 21(26):5406-16. PubMed ID: 23010473
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neurofibromin and NF1 gene analysis in composite pheochromocytoma and tumors associated with von Recklinghausen's disease.
    Kimura N; Watanabe T; Fukase M; Wakita A; Noshiro T; Kimura I
    Mod Pathol; 2002 Mar; 15(3):183-8. PubMed ID: 11904334
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma.
    Burnichon N; Buffet A; Parfait B; Letouzé E; Laurendeau I; Loriot C; Pasmant E; Abermil N; Valeyrie-Allanore L; Bertherat J; Amar L; Vidaud D; Favier J; Gimenez-Roqueplo AP
    Hum Mol Genet; 2012 Dec; 21(26):5397-405. PubMed ID: 22962301
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma.
    Burnichon N; Vescovo L; Amar L; Libé R; de Reynies A; Venisse A; Jouanno E; Laurendeau I; Parfait B; Bertherat J; Plouin PF; Jeunemaitre X; Favier J; Gimenez-Roqueplo AP
    Hum Mol Genet; 2011 Oct; 20(20):3974-85. PubMed ID: 21784903
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pheochromocytomas in Nf1 knockout mice express a neural progenitor gene expression profile.
    Powers JF; Evinger MJ; Zhi J; Picard KL; Tischler AS
    Neuroscience; 2007 Jul; 147(4):928-37. PubMed ID: 17582688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Immunohistochemical NF1 analysis does not predict NF1 gene mutation status in pheochromocytoma.
    Stenman A; Svahn F; Welander J; Gustavson B; Söderkvist P; Gimm O; Juhlin CC
    Endocr Pathol; 2015 Mar; 26(1):9-14. PubMed ID: 25403449
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.
    Gimm O; Armanios M; Dziema H; Neumann HP; Eng C
    Cancer Res; 2000 Dec; 60(24):6822-5. PubMed ID: 11156372
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Activating FGFR1 Mutations in Sporadic Pheochromocytomas.
    Welander J; Łysiak M; Brauckhoff M; Brunaud L; Söderkvist P; Gimm O
    World J Surg; 2018 Feb; 42(2):482-489. PubMed ID: 29159601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Frequent EPAS1/HIF2α exons 9 and 12 mutations in non-familial pheochromocytoma.
    Welander J; Andreasson A; Brauckhoff M; Bäckdahl M; Larsson C; Gimm O; Söderkvist P
    Endocr Relat Cancer; 2014 Jun; 21(3):495-504. PubMed ID: 24741025
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Topographic molecular profile of pheochromocytomas: role of somatic down-regulation of mismatch repair.
    Blanes A; Sanchez-Carrillo JJ; Diaz-Cano SJ
    J Clin Endocrinol Metab; 2006 Mar; 91(3):1150-8. PubMed ID: 16394087
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.
    Dannenberg H; van Nederveen FH; Abbou M; Verhofstad AA; Komminoth P; de Krijger RR; Dinjens WN
    J Clin Oncol; 2005 Mar; 23(9):1894-901. PubMed ID: 15774781
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs).
    Upadhyaya M; Kluwe L; Spurlock G; Monem B; Majounie E; Mantripragada K; Ruggieri M; Chuzhanova N; Evans DG; Ferner R; Thomas N; Guha A; Mautner V
    Hum Mutat; 2008 Jan; 29(1):74-82. PubMed ID: 17960768
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetics and biology of pheochromocytoma.
    Mannelli M; Simi L; Gaglianò MS; Opocher G; Ercolino T; Becherini L; Parenti G
    Exp Clin Endocrinol Diabetes; 2007 Mar; 115(3):160-5. PubMed ID: 17427103
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type I.
    Gutmann DH; Cole JL; Stone WJ; Ponder BA; Collins FS
    Genes Chromosomes Cancer; 1994 May; 10(1):55-8. PubMed ID: 7519874
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Germline and somatic NF1 gene mutations in plexiform neurofibromas.
    Upadhyaya M; Spurlock G; Monem B; Thomas N; Friedrich RE; Kluwe L; Mautner V
    Hum Mutat; 2008 Aug; 29(8):E103-11. PubMed ID: 18484666
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Loss of neurofibromatosis type I (NF1) gene expression in pheochromocytomas from patients without NF1.
    Gutmann DH; Geist RT; Rose K; Wallin G; Moley JF
    Genes Chromosomes Cancer; 1995 Jun; 13(2):104-9. PubMed ID: 7542904
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Malignant pheochromocytoma in a 16-year-old patient with neurofibromatosis type 1.
    Giovannoni I; Callea F; Boldrini R; Inserra A; Cozza R; Francalanci P
    Pediatr Dev Pathol; 2014; 17(2):126-9. PubMed ID: 24555864
    [TBL] [Abstract][Full Text] [Related]  

  • 20. From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytoma.
    Lepoutre-Lussey C; Thibault C; Buffet A; Morin A; Badoual C; Bénit P; Rustin P; Ottolenghi C; Janin M; Castro-Vega LJ; Trapman J; Gimenez-Roqueplo AP; Favier J
    Mol Cell Endocrinol; 2016 Feb; 421():40-8. PubMed ID: 26123588
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.