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 *

117 related articles for article (PubMed ID: 12687660)

  • 1. Homozygous inactivation of NF1 gene in a patient with familial NF1 and disseminated neuroblastoma.
    Origone P; Defferrari R; Mazzocco K; Lo Cunsolo C; De Bernardi B; Tonini GP
    Am J Med Genet A; 2003 May; 118A(4):309-13. PubMed ID: 12687660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fluorescence in situ hybridization analyses of chromosome band 1p36 in neuroblastoma detect two classes of alterations.
    Spitz R; Hero B; Westermann F; Ernestus K; Schwab M; Berthold F
    Genes Chromosomes Cancer; 2002 Jul; 34(3):299-305. PubMed ID: 12007190
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygous deletion of the neurofibromatosis-1 gene in the tumor of a patient with neuroblastoma.
    Martinsson T; Sjöberg RM; Hedborg F; Kogner P
    Cancer Genet Cytogenet; 1997 Jun; 95(2):183-9. PubMed ID: 9169039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of heterozygosity for chromosome 1p in familial neuroblastoma.
    Tonini GP; Lo Cunsolo C; Cusano R; Iolascon A; Dagnino M; Conte M; Milanaccio C; De Bernardi B; Mazzocco K; Scaruffi P
    Eur J Cancer; 1997 Oct; 33(12):1953-6. PubMed ID: 9516831
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome band 11q23 deletion predicts poor prognosis in bone marrow metastatic neuroblastoma patients without MYCN amplification.
    Yue ZX; Xing TY; Gao C; Liu SG; Zhao W; Zhao Q; Wang XS; Jin M; Ma XL
    Cancer Commun (Lond); 2019 Nov; 39(1):68. PubMed ID: 31685009
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations.
    Serra E; Ars E; Ravella A; Sánchez A; Puig S; Rosenbaum T; Estivill X; Lázaro C
    Hum Genet; 2001 May; 108(5):416-29. PubMed ID: 11409870
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromata.
    Leppig KA; Kaplan P; Viskochil D; Weaver M; Ortenberg J; Stephens K
    Am J Med Genet; 1997 Dec; 73(2):197-204. PubMed ID: 9409873
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome.
    Riva P; Castorina P; Manoukian S; Dalprà L; Doneda L; Marini G; den Dunnen J; Larizza L
    Hum Genet; 1996 Dec; 98(6):646-50. PubMed ID: 8931693
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A nonsense mutation at Arg-1947 in the NF1 gene in a case of neurofibromatosis type 1 in a Korean patient.
    Park KC; Choi HO; Park KH; Kim KH; Eun HC
    J Hum Genet; 2000; 45(2):84-5. PubMed ID: 10721668
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ten novel mutations in the human neurofibromatosis type 1 (NF1) gene in Italian patients.
    Origone P; De Luca A; Bellini C; Buccino A; Mingarelli R; Costabel S; La Rosa C; Garrè C; Coviello DA; Ajmar F; Dallapiccola B; Bonioli E
    Hum Mutat; 2002 Jul; 20(1):74-5. PubMed ID: 12112660
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Correlation of modified Shimada classification with MYCN and 1p36 status detected by fluorescence in situ hybridization in neuroblastoma.
    Altungoz O; Aygun N; Tumer S; Ozer E; Olgun N; Sakizli M
    Cancer Genet Cytogenet; 2007 Jan; 172(2):113-9. PubMed ID: 17213019
    [TBL] [Abstract][Full Text] [Related]  

  • 13. NF1 mutation analysis using a combined heteroduplex/SSCP approach.
    Abernathy CR; Rasmussen SA; Stalker HJ; Zori R; Driscoll DJ; Williams CA; Kousseff BG; Wallace MR
    Hum Mutat; 1997; 9(6):548-54. PubMed ID: 9195229
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exonic deletions in the NF1 gene in patients with neurofibromatosis type I from the lower Silesian region of Poland.
    Laczmańska I; Szczepaniak M; Jakubiak A; Stembalska A
    Adv Clin Exp Med; 2014; 23(4):517-21. PubMed ID: 25166435
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?
    Yang CC; Happle R; Chao SC; Yu-Yun Lee J; Chen W
    J Am Acad Dermatol; 2008 Mar; 58(3):493-7. PubMed ID: 18280349
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia.
    Boudry-Labis E; Roche-Lestienne C; Nibourel O; Boissel N; Terre C; Perot C; Eclache V; Gachard N; Tigaud I; Plessis G; Cuccuini W; Geffroy S; Villenet C; Figeac M; Leprêtre F; Renneville A; Cheok M; Soulier J; Dombret H; Preudhomme C;
    Am J Hematol; 2013 Apr; 88(4):306-11. PubMed ID: 23460398
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor development.
    Lo Cunsolo C; Iolascon A; Cavazzana A; Cusano R; Strigini P; Mazzocco K; Giordani L; Massimo L; De Bernardi B; Conte M; Tonini GP
    Cancer Genet Cytogenet; 1999 Mar; 109(2):126-30. PubMed ID: 10087945
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Caspase-9 and Apaf-1 are expressed and functionally active in human neuroblastoma tumor cell lines with 1p36 LOH and amplified MYCN.
    Teitz T; Wei T; Liu D; Valentine V; Valentine M; Grenet J; Lahti JM; Kidd VJ
    Oncogene; 2002 Mar; 21(12):1848-58. PubMed ID: 11896617
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A search for evidence of somatic mutations in the NF1 gene.
    John AM; Ruggieri M; Ferner R; Upadhyaya M
    J Med Genet; 2000 Jan; 37(1):44-9. PubMed ID: 10633134
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene.
    Colman SD; Williams CA; Wallace MR
    Nat Genet; 1995 Sep; 11(1):90-2. PubMed ID: 7550323
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.