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2002
Mark Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.
Irshaid, Nidal M ; Eicher, Nicole I ; Hustinx, Hein ; Poole, Joyce and Olsson, Martin L ^LU (2002) In British Journal of Haematology 116(2). p.445-453
- Contribution to journal › Article
Mark Hypoxia alters gene expression in human neuroblastoma cells toward an immature and neural crest-like phenotype.
Jögi, Annika ^LU ; Øra, Ingrid ^LU ; Nilsson, Helén ^LU ; Lindeheim, Åsa ^LU ; Makino, Yuichi ; Poellinger, Lorenz ; Axelson, Håkan ^LU and Påhlman, Sven ^LU (2002) In Proceedings of the National Academy of Sciences 99(10). p.7021-7026
- Contribution to journal › Article
Mark Neuropathological and behavioral consequences of adeno-associated viral vector-mediated continuous intrastriatal neurotrophin delivery in a focal ischemia model in rats.
Andsberg, Gunnar ^LU ; Kokaia, Zaal ^LU ; Klein, Ronald L ; Muzyczka, Nicholas ; Lindvall, Olle ^LU and Mandel, Ronald J (2002) In Neurobiology of Disease 9(2). p.187-204
- Contribution to journal › Article
Mark Genetic links between the acute-phase response and arthritis development in rats.
Olofsson, Peter ^LU ; Nordquist, Niklas ; Vingsbo-Lundberg, Carina ; Larsson, Anders ; Falkenberg, Cecilia ^LU ; Pettersson, Ulf ; Åkerström, Bo ^LU and Holmdahl, Rikard ^LU (2002) In Arthritis and Rheumatism 46(1). p.259-268
- Contribution to journal › Article
Mark The genetic control of sialadenitis versus arthritis in a NOD.QxB10.Q F2 cross.
Johansson, Åsa ^LU ; Nakken, Britt ; Sundler, Martin ; Lindqvist, Anna-Karin ^LU ; Johannesson, Martina ^LU ; Alarcón-Riquelme, Marta ; Bolstad, Anne Isine ; Humphreys-Beher, Michael G ; Jonsson, Roland and Skarstein, Kathrine , et al. (2002) In European Journal of Immunology 32(1). p.243-250
- Contribution to journal › Article
2001
Mark Clinical expressions of juvenile hereditary retinal degenerations and macular dystrophies: Electrophysiological and genetic studies
Eksandh, Louise ^LU (2001)
- Thesis › Doctoral thesis (compilation)
Mark Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
Zhao, F ; Weismann, C G ^LU ; Satoda, M ; Pierpont, M E ; Sweeney, E ; Thompson, E M and Gelb, B D (2001) In American Journal of Human Genetics 69(4). p.695-703
- Contribution to journal › Article
Mark Clinical implications of mutations of neutrophil elastase in congenital and cyclic neutropenia
Dale, David C ; Liles, W Conrad ; Garwicz, Daniel ^LU and Aprikyan, Andrew G (2001) In Journal of Pediatric Hematology/Oncology 23(4). p.10-208
- Contribution to journal › Debate/Note/Editorial
2000
Mark Sunscreen use and malignant melanoma
Westerdahl, J ^LU ; Ingvar, C ^LU ; Mâsbäck, A ^LU and Olsson, Håkan ^LU (2000) In International Journal of Cancer 87(1). p.145-150
- Contribution to journal › Article
Mark p53-mediated differentiation of the erythroleukemia cell line K562
Chylicki, K ; Ehinger, M ^LU ; Svedberg, H ^LU ; Bergh, G ^LU ; Olsson, I ^LU and Gullberg, U ^LU (2000) In Cell Growth and Differentiation 11(6). p.24-315
- Contribution to journal › Article

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