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Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours.
Schoenmakers EF, Wanschura S, Mols R, Bullerdiek J, Van den Berghe H, Van de Ven WJ. Schoenmakers EF, et al. Nat Genet. 1995 Aug;10(4):436-44. doi: 10.1038/ng0895-436. Nat Genet. 1995. PMID: 7670494
Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12.
Wanschura S, Belge G, Stenman G, Kools P, Dal Cin P, Schoenmakers E, Huysmans C, Van den Berghe H, Bartnitzke S, Van de Ven WJ, Bullerdiek J. Wanschura S, et al. Among authors: schoenmakers e. Cancer Genet Cytogenet. 1996 Jan;86(1):39-45. doi: 10.1016/0165-4608(95)00164-6. Cancer Genet Cytogenet. 1996. PMID: 8616784
Cumulative dosage effect of a RAD51L1/HMGA2 fusion and RAD51L1 loss in a case of pseudo-Meigs' syndrome.
Amant F, Debiec-Rychter M, Schoenmakers EF, Hagemeijer-Hausman A, Vergote I. Amant F, et al. Among authors: schoenmakers ef. Genes Chromosomes Cancer. 2001 Dec;32(4):324-9. doi: 10.1002/gcc.1197. Genes Chromosomes Cancer. 2001. PMID: 11746973
LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes.
Petit MM, Schoenmakers EF, Huysmans C, Geurts JM, Mandahl N, Van de Ven WJ. Petit MM, et al. Among authors: schoenmakers ef. Genomics. 1999 May 1;57(3):438-41. doi: 10.1006/geno.1999.5778. Genomics. 1999. PMID: 10329012
Expression of reciprocal hybrid transcripts of HMGIC and FHIT in a pleomorphic adenoma of the parotid gland.
Geurts JM, Schoenmakers EF, Röijer E, Stenman G, Van de Ven WJ. Geurts JM, et al. Among authors: schoenmakers ef. Cancer Res. 1997 Jan 1;57(1):13-7. Cancer Res. 1997. PMID: 8988031
Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasia.
Groenen PM, Garcia E, Thoelen R, Aly M, Schoenmakers EF, Devriendt K, Fryns JP, Van de Ven WJ. Groenen PM, et al. Among authors: schoenmakers ef. Cytogenet Cell Genet. 1996;75(4):210-5. doi: 10.1159/000134485. Cytogenet Cell Genet. 1996. PMID: 9067426
Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3'/4 synpolydactyly.
Debeer P, Schoenmakers EF, Thoelen R, Fryns JP, Van de Ven WJ. Debeer P, et al. Among authors: schoenmakers ef. Cytogenet Cell Genet. 1998;81(3-4):229-34. doi: 10.1159/000015036. Cytogenet Cell Genet. 1998. PMID: 9730609
Complex genomic rearrangement within the 12q15 multiple aberration region induced by integrated human papillomavirus 18 in a cervical carcinoma cell line.
Gallego MI, Schoenmakers EF, Van de Ven WJ, Lazo PA. Gallego MI, et al. Among authors: schoenmakers ef. Mol Carcinog. 1997 Jun;19(2):114-21. doi: 10.1002/(sici)1098-2744(199707)19:2<114::aid-mc6>3.0.co;2-f. Mol Carcinog. 1997. PMID: 9210958
Genomic organization of the human NSP gene, prototype of a novel gene family encoding reticulons.
Roebroek AJ, Ayoubi TA, Van de Velde HJ, Schoenmakers EF, Pauli IG, Van de Ven WJ. Roebroek AJ, et al. Among authors: schoenmakers ef. Genomics. 1996 Mar 1;32(2):191-9. doi: 10.1006/geno.1996.0105. Genomics. 1996. PMID: 8833145
Identification of NFIB as recurrent translocation partner gene of HMGIC in pleomorphic adenomas.
Geurts JM, Schoenmakers EF, Röijer E, Aström AK, Stenman G, van de Ven WJ. Geurts JM, et al. Among authors: schoenmakers ef. Oncogene. 1998 Feb 19;16(7):865-72. doi: 10.1038/sj.onc.1201609. Oncogene. 1998. PMID: 9484777
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