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.
198 related articles for article (PubMed ID: 21031597)
1. Dissecting loss of heterozygosity (LOH) in neurofibromatosis type 1-associated neurofibromas: Importance of copy neutral LOH. Garcia-Linares C; Fernández-Rodríguez J; Terribas E; Mercadé J; Pros E; Benito L; Benavente Y; Capellà G; Ravella A; Blanco I; Kehrer-Sawatzki H; Lázaro C; Serra E Hum Mutat; 2011 Jan; 32(1):78-90. PubMed ID: 21031597 [TBL] [Abstract][Full Text] [Related]
2. Mechanisms of loss of heterozygosity in neurofibromatosis type 1-associated plexiform neurofibromas. Steinmann K; Kluwe L; Friedrich RE; Mautner VF; Cooper DN; Kehrer-Sawatzki H J Invest Dermatol; 2009 Mar; 129(3):615-21. PubMed ID: 18800150 [TBL] [Abstract][Full Text] [Related]
3. Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1. Rasmussen SA; Overman J; Thomson SA; Colman SD; Abernathy CR; Trimpert RE; Moose R; Virdi G; Roux K; Bauer M; Rojiani AM; Maria BL; Muir D; Wallace MR Genes Chromosomes Cancer; 2000 Aug; 28(4):425-31. PubMed ID: 10862051 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis. Margraf RL; VanSant-Webb C; Sant D; Carey J; Hanson H; D'Astous J; Viskochil D; Stevenson DA; Mao R J Mol Diagn; 2017 May; 19(3):468-474. PubMed ID: 28433079 [TBL] [Abstract][Full Text] [Related]
6. Characterization of the somatic mutational spectrum of the neurofibromatosis type 1 (NF1) gene in neurofibromatosis patients with benign and malignant tumors. Upadhyaya M; Han S; Consoli C; Majounie E; Horan M; Thomas NS; Potts C; Griffiths S; Ruggieri M; von Deimling A; Cooper DN Hum Mutat; 2004 Feb; 23(2):134-146. PubMed ID: 14722917 [TBL] [Abstract][Full Text] [Related]
7. Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene. Däschner K; Assum G; Eisenbarth I; Krone W; Hoffmeyer S; Wortmann S; Heymer B; Kehrer-Sawatzki H Biochem Biophys Res Commun; 1997 May; 234(2):346-50. PubMed ID: 9177273 [TBL] [Abstract][Full Text] [Related]
8. Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patients. De Raedt T; Maertens O; Chmara M; Brems H; Heyns I; Sciot R; Majounie E; Upadhyaya M; De Schepper S; Speleman F; Messiaen L; Vermeesch JR; Legius E Genes Chromosomes Cancer; 2006 Oct; 45(10):893-904. PubMed ID: 16830335 [TBL] [Abstract][Full Text] [Related]
9. Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1. Eisenbarth I; Beyer K; Krone W; Assum G Am J Hum Genet; 2000 Feb; 66(2):393-401. PubMed ID: 10677298 [TBL] [Abstract][Full Text] [Related]
10. Analysis of NF1 somatic mutations in cutaneous neurofibromas from patients with high tumor burden. Thomas L; Kluwe L; Chuzhanova N; Mautner V; Upadhyaya M Neurogenetics; 2010 Oct; 11(4):391-400. PubMed ID: 20358387 [TBL] [Abstract][Full Text] [Related]
11. The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas. Upadhyaya M; Spurlock G; Kluwe L; Chuzhanova N; Bennett E; Thomas N; Guha A; Mautner V Neurogenetics; 2009 Jul; 10(3):251-63. PubMed ID: 19221814 [TBL] [Abstract][Full Text] [Related]
12. Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies. Stephens K; Weaver M; Leppig KA; Maruyama K; Emanuel PD; Le Beau MM; Shannon KM Blood; 2006 Sep; 108(5):1684-9. PubMed ID: 16690971 [TBL] [Abstract][Full Text] [Related]
13. Single-cell PCR performed with neurofibroma Schwann cells reveals the presence of both alleles of the neurofibromatosis type 1 (NF1) gene. Stark M; Assum G; Krone W Hum Genet; 1995 Nov; 96(5):619-23. PubMed ID: 8530015 [TBL] [Abstract][Full Text] [Related]
14. Confirmation of a double-hit model for the NF1 gene in benign neurofibromas. Serra E; Puig S; Otero D; Gaona A; Kruyer H; Ars E; Estivill X; Lázaro C Am J Hum Genet; 1997 Sep; 61(3):512-9. PubMed ID: 9326316 [TBL] [Abstract][Full Text] [Related]
15. Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumors. Stewart DR; Pemov A; Van Loo P; Beert E; Brems H; Sciot R; Claes K; Pak E; Dutra A; Lee CC; Legius E Genes Chromosomes Cancer; 2012 May; 51(5):429-37. PubMed ID: 22250039 [TBL] [Abstract][Full Text] [Related]
16. Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromas. Serra E; Rosenbaum T; Nadal M; Winner U; Ars E; Estivill X; Lázaro C Nat Genet; 2001 Jul; 28(3):294-6. PubMed ID: 11431704 [TBL] [Abstract][Full Text] [Related]
17. Tumor and Constitutional Sequencing for Neurofibromatosis Type 1. Tong S; Devine WP; Shieh JT JCO Precis Oncol; 2022 May; 6():e2100540. PubMed ID: 35584348 [TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing of breast cancer, malignant peripheral nerve sheath tumor and neurofibroma from a patient with neurofibromatosis type 1. McPherson JR; Ong CK; Ng CC; Rajasegaran V; Heng HL; Yu WS; Tan BK; Madhukumar P; Teo MC; Ngeow J; Thike AA; Rozen SG; Tan PH; Lee AS; Teh BT; Yap YS Cancer Med; 2015 Dec; 4(12):1871-8. PubMed ID: 26432421 [TBL] [Abstract][Full Text] [Related]
19. KIR2DL5 mutation and loss underlies sporadic dermal neurofibroma pathogenesis and growth. Anastasaki C; Dahiya S; Gutmann DH Oncotarget; 2017 Jul; 8(29):47574-47585. PubMed ID: 28548933 [TBL] [Abstract][Full Text] [Related]
20. Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors. Beert E; Brems H; Daniëls B; De Wever I; Van Calenbergh F; Schoenaers J; Debiec-Rychter M; Gevaert O; De Raedt T; Van Den Bruel A; de Ravel T; Cichowski K; Kluwe L; Mautner V; Sciot R; Legius E Genes Chromosomes Cancer; 2011 Dec; 50(12):1021-32. PubMed ID: 21987445 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]