Background splicing as a predictor of aberrant splicing in genetic disease von Alexieva, Diana, Long, Yi, Sarkar, Rupa, Dhayan, Hansraj, Bruet, Emmanuel, Winston, Robert Maurice, Vorechovsky, Igor, Castellano, Leandro, Dibb, Nicholas John

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DBASS3 and DBASS5: databases of aberrant 3'- and 5'-splice sites von Buratti, Emanuele, Chivers, Martin, Hwang, Gyulin, Vorechovsky, Igor

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Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID) von Hammarström, L., Vorechovsky, I., Webster, D.

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Deletion and reduced expression of the fanconi anemia FANCA gene in sporadic acute myeloid leukemia von TISCHKOWITZ, M. D, MORGAN, N. V, GRIMWADE, D, EDDY, C, BALL, S, VORECHOVSKY, I, LANGABEER, S, STÖGER, R, HODGSON, S. V, MATHEW, C. G

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Colocalization of X-Linked Agammaglobulinemia and X-Linked Immunodeficiency Genes von Thomas, Jeffrey D., Sideras, Paschalis, C. I. Edvard Smith, Vořechovský, Igor, Chapman, Verne, Paul, William E.

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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... von Vořechovský, Igor, Webster, A. David B., Plebani, Alessandro, Hammarström, Lennart

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Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia von VORECHOVSKY, I, LUO, L, DYER, M. J. S, CATOVSKY, D, AMLOT, P. L, YAXLEY, J. C, FORONI, L, HAMMARSTRÖM, L, WEBSTER, A. D. B, YUILLE, M. A. R

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Why do we see JAK2 exon 12 mutations in myeloproliferative neoplasms? von Vorechovsky, I, Jones, A V, Cross, N C P

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The ATM gene and susceptibility to breast cancer : Analysis of 38 breast tumors reveals no evidence for mutation von VORECHOVSKY, I, RASIO, D, CROCE, C. M, NEGRINI, M, LUO, L, MONACO, C, HAMMARSTRÖM, L, WEBSTER, A. D. B, ZALOUDIK, J, BARBANTI-BRODANO, G, JAMES, M, RUSSO, G

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Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene : Support for a gatekeeper mechanism in skin tumorigenesis von VORECHOVSKY, I, UNDEN, A. B, SANDSTEDT, B, TOFTGARD, R, STAHLE-BÄCKDAHL, M

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ATM is usually rearranged in T-cell prolymphocytic leukaemia von YUILLE, M. A. R, COIGNET, L. J. A, ABRAHAM, S. M, YAQUB, F, LUO, L, MATUTES, E, BRITO-BABAPULLE, V, VORECHOVSKY, I, DYER, M. J. S, CATOVSKY, D

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ATM Mutations in cancer families von VORECHOVSKY, I, LUO, L, LINDBLOM, A, NEGRINI, M, WEBSTER, A. D. B, CROCE, C. M, HAMMARSTRÖM, L

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Patched (ptch)-associated preferential expression of smoothened (smoh) in human basal cell carcinoma of the skin von KALLASSY, M, TOFTGARD, R, UEDA, M, NAKAZAWA, K, VORECHOVSKY, I, YAMASAKI, H, NAKAZAWA, H

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BTKbase, Mutation Database for X-Linked Agammaglobulinemia (XLA) von Vihinen, Mauno, Iwata, Tsutomu, Kinnon, Christine, Kwan, Sau-Ping, Ochs, Hans D., Vorechovsky, Igor, Smith, C. I. Edvard

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Missense mutations at ATM gene and cancer risk von Vorechovsky, I, Ortmann, E, Steinmann, D, Dörk, T

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Ataxia-telangiectasia and T-cell leukemias : No evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLL von LIPING LUO, LU, F.-M, HART, S, FORONI, L, RABBANI, H, HAMMARSTRÖM, L, WEBSTER, A. D. B, VORECHOVSKY, I

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Antisense Oligonucleotides Modulating Activation of a Nonsense-Mediated RNA Decay Switch Exon in the ATM Gene von Kralovicova, Jana, Moreno, Pedro M.D., Cross, Nicholas C.P., Pêgo, Ana Paula, Vorechovsky, Igor

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Compensatory signals associated with the activation of human GC 5' splice sites von Kralovicova, Jana, Hwang, Gyulin, Asplund, A Charlotta, Churbanov, Alexander, Smith, C I Edvard, Vorechovsky, Igor

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Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome von Hahn, Heidi, Wicking, Carol, Zaphiropoulos, Peter G, Gailani, Mae R, Shanley, Susan, Chidambaram, Abirami, Vorechovsky, Igor, Holmberg, Erika, Unden, Anne Birgitte, Gillies, Susan, Negus, Kylie, Smyth, Ian, Pressman, Carolyn, Leffell, David J, Gerrard, Bernard, Goldstein, Alisa M, Dean, Michael, Toftgard, Rune, Chenevix-Trench, Georgia, Wainwright, Brandon, Bale, Allen E

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Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case fami... von Vorechovský, I, Cullen, M, Carrington, M, Hammarström, L, Webster, A D

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