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Results: 1-25 | 26-32
Results: 1-25/32
Bioinformatics in proteomics
Authors: Vihinen, M
Citation: M. Vihinen, Bioinformatics in proteomics, BIOMOL ENG, 18(5), 2001, pp. 241-248
BioWAP, mobile Internet service for bioinformatics
Authors: Riikonen, P Boberg, J Salakoski, T Vihinen, M
Citation: P. Riikonen et al., BioWAP, mobile Internet service for bioinformatics, BIOINFORMAT, 17(9), 2001, pp. 855-856
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency
Authors: Notorangelo, LD Mella, P Jones, A Baisle, GD Savoldi, G Cranston, T Vihinen, M Schumacher, RF
Citation: Ld. Notorangelo et al., Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency, HUM MUTAT, 18(4), 2001, pp. 255-263
The mutational spectrum of human malignant autosomal recessive osteopetrosis
Authors: Sobacchi, C Frattini, A Orchard, P Porras, O Tezcan, I Andolina, M Babul-Hirji, R Baric, I Canham, N Chitayat, D Dupuis-Girod, S Ellis, I Etzioni, A Fasth, A Fisher, A Gerritsen, B Gulino, V Horwitz, E Klamroth, V Lanino, E Mirolo, M Musio, A Matthijs, G Nonomaya, S Notarangelo, LD Ochs, HD Furga, AS Valiaho, J van Hove, JLK Vihinen, M Vujic, D Vezzoni, P Villa, A
Citation: C. Sobacchi et al., The mutational spectrum of human malignant autosomal recessive osteopetrosis, HUM MOL GEN, 10(17), 2001, pp. 1767-1773
Distinct gene expression profiling in chronic lymphocytic leukemia with 11q23 deletion
Authors: Aalto, Y El-Rifai, W Vilpo, L Ollila, J Nagy, B Vihinen, M Vilpo, J Knuutila, S
Citation: Y. Aalto et al., Distinct gene expression profiling in chronic lymphocytic leukemia with 11q23 deletion, LEUKEMIA, 15(11), 2001, pp. 1721-1728
Coevolution of the domains of cytoplasmic tyrosine kinases
Authors: Nars, M Vihinen, M
Citation: M. Nars et M. Vihinen, Coevolution of the domains of cytoplasmic tyrosine kinases, MOL BIOL EV, 18(3), 2001, pp. 312-321
Analysis of Btk mutations in patients with X-linked agammaglobulinaemia (XLA) and determination of carrier status in normal female relatives: a nationwide study of Btk deficiency in Greece
Authors: Speletas, M Kanariou, M Kanakoudi-Tsakalidou, F Papadopoulou-Alataki, E Arvanitidis, K Pardali, E Constantopoulos, A Kartalis, G Vihinen, M Sideras, P Ritis, K
Citation: M. Speletas et al., Analysis of Btk mutations in patients with X-linked agammaglobulinaemia (XLA) and determination of carrier status in normal female relatives: a nationwide study of Btk deficiency in Greece, SC J IMMUN, 54(3), 2001, pp. 321-327
The Tec family of cytoplasmic tyrosine kinases: mammalian Btk, Bmx, Itk, Tec, Txk and homologs in other species
Authors: Smith, CIE Islam, TC Mattsson, PT Mohamed, AJ Nore, BF Vihinen, M
Citation: Cie. Smith et al., The Tec family of cytoplasmic tyrosine kinases: mammalian Btk, Bmx, Itk, Tec, Txk and homologs in other species, BIOESSAYS, 23(5), 2001, pp. 436-446
Molecular dynamics simulation of the effects of cytosine methylation on structure of oligonucleotides
Authors: Norberg, J Vihinen, M
Citation: J. Norberg et M. Vihinen, Molecular dynamics simulation of the effects of cytosine methylation on structure of oligonucleotides, J MOL ST-TH, 546, 2001, pp. 51-62
Intermolecular interactions between the SH3 domain and the proline-rich THregion of Bruton's tyrosine kinase
Authors: Hansson, H Okoh, MP Smith, CIE Vihinen, M Hard, T
Citation: H. Hansson et al., Intermolecular interactions between the SH3 domain and the proline-rich THregion of Bruton's tyrosine kinase, FEBS LETTER, 489(1), 2001, pp. 67-70
On preprocessing of protein sequences for neural network prediction of polyproline type II secondary structures
Authors: Siermala, M Juhola, M Vihinen, M
Citation: M. Siermala et al., On preprocessing of protein sequences for neural network prediction of polyproline type II secondary structures, COMPUT BIOL, 31(5), 2001, pp. 385-398
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations
Authors: Villa, A Sobacchi, C Notarangelo, LD Bozzi, F Abinun, M Abrahamsen, TG Arkwright, PD Baniyash, M Brooks, EG Conley, ME Cortes, P Duse, M Fasth, A Filipovich, AM Infante, AJ Jones, A Mazzolari, E Muller, SM Pasic, S Rechavi, G Sacco, MG Santagata, S Schroeder, ML Seger, R Strina, D Ugazio, A Valiaho, J Vihinen, M Vogler, LB Ochs, H Vezzoni, P Friedrich, W Schwarz, K
Citation: A. Villa et al., V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations, BLOOD, 97(1), 2001, pp. 81-88
Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency
Authors: Vihinen, M Villa, A Mella, P Schumacher, RF Savoldi, G O'Shea, JJ Candotti, F Notarangelo, LD
Citation: M. Vihinen et al., Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency, CLIN IMMUNO, 96(2), 2000, pp. 108-118
Bruton tyrosine kinase (Btk) in X-linked agammaglobulinemia (XLA)
Authors: Vihinen, M Mattsson, PT Smith, CIE
Citation: M. Vihinen et al., Bruton tyrosine kinase (Btk) in X-linked agammaglobulinemia (XLA), FRONT BIOSC, 5, 2000, pp. D917-D927
Structural basis of bloom syndrome (BS) causing mutations in the BLM helicase domain
Authors: Rong, SB Valiaho, J Vihinen, M
Citation: Sb. Rong et al., Structural basis of bloom syndrome (BS) causing mutations in the BLM helicase domain, MOL MED, 6(3), 2000, pp. 155-164
Rational design and purification of human Bruton's tyrosine kinase SH3-SH2protein for structure-function studies
Authors: Nera, KP Brockmann, E Vihinen, M Smith, CIE Mattsson, PT
Citation: Kp. Nera et al., Rational design and purification of human Bruton's tyrosine kinase SH3-SH2protein for structure-function studies, PROT EX PUR, 20(3), 2000, pp. 365-371
Structural basis of Wiskott-Aldrich syndrome causing mutations in the WH1 domain
Authors: Rong, SB Vihinen, M
Citation: Sb. Rong et M. Vihinen, Structural basis of Wiskott-Aldrich syndrome causing mutations in the WH1 domain, J MOL MED-J, 78(9), 2000, pp. 530-537
Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family
Authors: Aapola, U Shibuya, K Scott, HS Ollila, J Vihinen, M Heino, M Shintani, A Kawasaki, K Minoshima, S Krohn, K Antonarakis, SE Shimizu, N Kudoh, J Peterson, P
Citation: U. Aapola et al., Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family, GENOMICS, 65(3), 2000, pp. 293-298
KinMutBase, a database of human disease-causing protein kinase mutations
Authors: Stenberg, KAE Riikonen, PT Vihinen, M
Citation: Kae. Stenberg et al., KinMutBase, a database of human disease-causing protein kinase mutations, NUCL ACID R, 28(1), 2000, pp. 369-371
Structure-function effects in primary immunodeficiencies
Authors: Korpi, M Valiaho, J Vihinen, M
Citation: M. Korpi et al., Structure-function effects in primary immunodeficiencies, SC J IMMUN, 52(3), 2000, pp. 226-232
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
Authors: Notarangelo, LD Giliani, S Mazza, C Mella, P Savoldi, G Rodriguez-Perez, C Mazzolari, E Fiorini, M Duse, M Plebani, A Ugazio, AG Vihinen, M Candotti, F Schumacher, RF
Citation: Ld. Notarangelo et al., Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model, IMMUNOL REV, 178, 2000, pp. 39-48
Novel immunodeficiency data servers
Authors: Valiaho, L Riikonen, P Vihinen, M
Citation: L. Valiaho et al., Novel immunodeficiency data servers, IMMUNOL REV, 178, 2000, pp. 177-185
Six X-linked agammaglobulinemia-causing missense mutations in the src homology 2 domain of Bruton's tyrosine kinase: Phosphotyrosine-binding and circular dichroism analysis
Authors: Mattsson, PT Lappalainen, I Backesjo, CM Brockmann, E Lauren, S Vihinen, M Smith, CIE
Citation: Pt. Mattsson et al., Six X-linked agammaglobulinemia-causing missense mutations in the src homology 2 domain of Bruton's tyrosine kinase: Phosphotyrosine-binding and circular dichroism analysis, J IMMUNOL, 164(8), 2000, pp. 4170-4177
The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein
Authors: Pitkanen, J Doucas, V Sternsdorf, T Nakajima, T Aratani, S Jensen, K Will, H Vahamurto, P Ollila, J Vihinen, M Scott, HS Antonarakis, SE Kudoh, J Shimizu, N Krohn, K Peterson, P
Citation: J. Pitkanen et al., The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein, J BIOL CHEM, 275(22), 2000, pp. 16802-16809
Identification of novel transcription factor-like gene from human intestinal cells
Authors: Lindfors, K Halttunen, T Huotari, P Nupponen, N Vihinen, M Visakorpi, T Maki, M Kainulainen, H
Citation: K. Lindfors et al., Identification of novel transcription factor-like gene from human intestinal cells, BIOC BIOP R, 276(2), 2000, pp. 660-666
Risultati: 1-25 | 26-32