Mauno Vihinen

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2001
Mark Distinct gene expression profiling in chronic lymphocytic leukemia with 11q23 deletion
Aalto, Y ; El-Rifai, W ; Vilpo, L ; Ollila, J ; Nagy, B ; Vihinen, Mauno ^LU ; Vilpo, J and Knuutila, S (2001) In Leukemia 15(11). p.1721-1728
- Contribution to journal › Article
Mark Structural basis for immunodeficiency-causing mutations in the SH2 domains of BTK and SH2D1A
Lappalainen, L and Vihinen, Mauno ^LU (2001) Conference of the NATO Advanced-Study-Institute on Protein Modules in Cellular Signalling 318. p.96-103
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
Mark Molecular dynamics simulation of the effects of cytosine methylation on structure of oligonucleotides
Norberg, J and Vihinen, Mauno ^LU (2001) In Journal of molecular structure. Theochem 546. p.51-62
- Contribution to journal › Article
Mark The Tec family of cytoplasmic tyrosine kinases: mammalian Btk, Bmx, Itk, Tec, Txk and homologs in other species
Smith, CIE ; Islam, TC ; Mattsson, PT ; Mohamed, AJ ; Nore, BF and Vihinen, Mauno ^LU (2001) In BioEssays 23(5). p.436-446
- Contribution to journal › Scientific review
Mark 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
Speletas, M ; Kanariou, M ; Kanakoudi-Tsakalidou, F ; Papadopoulou-Alataki, E ; Arvanitidis, K ; Pardali, E ; Constantopoulos, A ; Kartalis, G ; Vihinen, Mauno ^LU and Sideras, P , et al. (2001) In Scandinavian Journal of Immunology 54(3). p.321-327
- Contribution to journal › Article
Mark Coevolution of the domains of cytoplasmic tyrosine kinases
Nars, M and Vihinen, Mauno ^LU (2001) In Molecular biology and evolution 18(3). p.312-321
- Contribution to journal › Article
Mark The mutational spectrum of human malignant autosomal recessive osteopetrosis
Sobacchi, C ; Frattini, A ; Orchard, P ; Porras, O ; Tezcan, I ; Andolina, M ; Babul-Hirji, R ; Baric, I ; Canham, N and Chitayat, D , et al. (2001) In Human Molecular Genetics 10(17). p.1767-1773
- Contribution to journal › Article
Mark V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations
Villa, A ; Sobacchi, C ; Notarangelo, LD ; Bozzi, F ; Abinun, M ; Abrahamsen, TG ; Arkwright, PD ; Baniyash, M ; Brooks, EG and Conley, ME , et al. (2001) In Blood 97(1). p.81-88
- Contribution to journal › Article
Mark On preprocessing of protein sequences for neural network prediction of polyproline type II secondary structures
Siermala, M ; Juhola, M and Vihinen, Mauno ^LU (2001) In Computers in Biology and Medicine 31(5). p.385-398
- Contribution to journal › Article
Mark Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency
Notorangelo, LD ; Mella, P ; Jones, A ; Baisle, GD ; Savoldi, G ; Cranston, T ; Vihinen, Mauno ^LU and Schumacher, RF (2001) In Human Mutation 18(4). p.255-263
- Contribution to journal › Article

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