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Results: 1-15 |
Results: 15
Low frequency of E-cadherin alterations in familial breast cancer
Authors: Salahshor, S Lei, HX Huo, HG Kristensen, VN Loman, N Sjoberg-Margolin, S Borg, A Borresen-Dale, AL Vorechovsky, I Lindblom, A
Citation: S. Salahshor et al., Low frequency of E-cadherin alterations in familial breast cancer, BREAST CA R, 3(3), 2001, pp. 199-207
Does 77C -> G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?
Authors: Vorechovsky, I Kralovicova, J Tchilian, E Masterman, T Zhang, ZP Ferry, B Misbah, S Chapel, H Webster, D Hellgren, D Anvret, M Hillert, J Hammarstrom, L Beverley, PC
Citation: I. Vorechovsky et al., Does 77C -> G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?, NAT GENET, 29(1), 2001, pp. 22-23
Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region
Authors: Vorechovsky, I Kralovicova, J Laycock, MD Webster, ADB Marsh, SGE Madrigal, A Hammarstrom, L
Citation: I. Vorechovsky et al., Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region, EUR J HUM G, 9(8), 2001, pp. 590-598
Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer
Authors: Forsti, A Luo, L Vorechovsky, I Soderberg, M Lichtenstein, P Hemminki, K
Citation: A. Forsti et al., Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer, CARCINOGENE, 22(1), 2001, pp. 27-33
Recurrent ATM mutations in T-PLL on diverse haplotypes: no support for their germline origin
Authors: Stankovic, T Taylor, AMR Yuille, MR Vorechovsky, I
Citation: T. Stankovic et al., Recurrent ATM mutations in T-PLL on diverse haplotypes: no support for their germline origin, BLOOD, 97(5), 2001, pp. 1517-1518
Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms
Authors: Calin, GA di Iasio, MG Caprini, E Vorechovsky, I Natali, PG Sozzi, G Croce, CM Barbanti-Brodano, G Russo, G Negrini, M
Citation: Ga. Calin et al., Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms, ONCOGENE, 19(9), 2000, pp. 1191-1195
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients
Authors: D'Errico, M Calcagnile, A Canzona, F Didona, B Posteraro, P Cavalieri, R Corona, R Vorechovsky, I Nardo, T Stefanini, M Dogliotti, E
Citation: M. D'Errico et al., UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patients, ONCOGENE, 19(3), 2000, pp. 463-467
Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: Identification and characterization of haplotypes shared by affected members of 101 multiple-case families
Authors: Vorechovsky, I Cullen, M Carrington, M Hammarstrom, L Webster, ADB
Citation: I. Vorechovsky et al., Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: Identification and characterization of haplotypes shared by affected members of 101 multiple-case families, J IMMUNOL, 164(8), 2000, pp. 4408-4416
Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)
Authors: Hammarstrom, L Vorechovsky, I Webster, D
Citation: L. Hammarstrom et al., Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID), CLIN EXP IM, 120(2), 2000, pp. 225-231
The patched/hedgehog/smoothened signalling pathway in human breast cancer:No evidence for H133YSHH, PTCH and SMO mutations
Authors: Vorechovsky, I Benediktsson, KP Toftgard, R
Citation: I. Vorechovsky et al., The patched/hedgehog/smoothened signalling pathway in human breast cancer:No evidence for H133YSHH, PTCH and SMO mutations, EUR J CANC, 35(5), 1999, pp. 711-713
Refinement of the LOH region 1 at 11q23.1 deleted in human breast carcinomas and sublocalization of 11 expressed sequence tags within the refined region
Authors: di Iasio, MG Calin, G Tibiletti, MG Vorechovsky, I Benediktsson, KP Taramelli, R Barbanti-Brodano, G Negrini, M
Citation: Mg. Di Iasio et al., Refinement of the LOH region 1 at 11q23.1 deleted in human breast carcinomas and sublocalization of 11 expressed sequence tags within the refined region, ONCOGENE, 18(8), 1999, pp. 1635-1638
Missense mutations at ATM gene and cancer risk (vol 354, pg 1276, 1999)
Authors: Vorechovsky, I
Citation: I. Vorechovsky, Missense mutations at ATM gene and cancer risk (vol 354, pg 1276, 1999), LANCET, 354(9180), 1999, pp. 780-780
Missense mutations at ATM gene and cancer risk
Authors: Vorechovsky, I Ortmann, E Steinmann, D Dork, T
Citation: I. Vorechovsky et al., Missense mutations at ATM gene and cancer risk, LANCET, 353(9160), 1999, pp. 1276-1276
A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: Evidence from meiotic mapping of 83 multiple-case families
Authors: Vorechovsky, I Blennow, E Nordenskjold, M Webster, ADB Hammarstrom, L
Citation: I. Vorechovsky et al., A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: Evidence from meiotic mapping of 83 multiple-case families, J IMMUNOL, 163(4), 1999, pp. 2236-2242
Genetic linkage of IgA deficiency to the major histocompatibility complex:Evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition
Authors: Vorechovsky, I Webster, ADB Plebani, A Hammarstrom, L
Citation: I. Vorechovsky et al., Genetic linkage of IgA deficiency to the major histocompatibility complex:Evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition, AM J HU GEN, 64(4), 1999, pp. 1096-1109
Risultati: 1-15 |