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2005
Mark The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient {beta}-cell mass and exocytosis.
Björkqvist, Maria ^LU ; Fex, Malin ^LU ; Renström, Erik ^LU ; Wierup, Nils ^LU ; Petersén, Åsa ^LU ; Gil, Joana ^LU ; Bacos, Karl ^LU ; Popovic, Natalija ^LU ; Li, Jia-Yi ^LU and Sundler, Frank ^LU , et al. (2005) In Human Molecular Genetics 14(5). p.565-574
- Contribution to journal › Article
Mark Orexin loss in Huntington's disease.
Petersén, Åsa ^LU ; Gil, Joana ^LU ; Maat-Schieman, Marion L C ; Björkqvist, Maria ^LU ; Tanila, Heikki ; Araújo, Ines M ; Smith, Ruben ^LU ; Popovic, Natalija ^LU ; Wierup, Nils ^LU and Norlén, Per ^LU , et al. (2005) In Human Molecular Genetics 14(1). p.39-47
- Contribution to journal › Article
Mark Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
Nuber, Ulrike ^LU ; Kriaucionis, Skirmantas ; Roloff, Tim C ; Guy, Jacky ; Selfridge, Jim ; Steinhoff, Christine ; Schulz, Ralph ; Lipkowitz, Bettina ; Ropers, H Hilger and Holmes, Megan C , et al. (2005) In Human Molecular Genetics 14(15). p.2247-2256
- Contribution to journal › Article
Mark Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy
Baker, N L ; Mörgelin, Matthias ^LU ; Peat, R ; Goemans, N ; North, K N ; Bateman, J F and Lamande, S R (2005) In Human Molecular Genetics 14(2). p.279-293
- Contribution to journal › Article
Mark Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22
Parsons, Claire A ; Mroczkowski, H Joel ; McGuigan, Fiona E A ^LU ; Albagha, Omar M E ; Manolagas, Stavros ; Reid, David M ; Ralston, Stuart H and Shmookler Reis, Robert J (2005) In Human Molecular Genetics 14(21). p.8-3141
- Contribution to journal › Article
2004
Mark Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3.
Koivukoski, Liisa ; Fisher, Sheila A. ; Kanninen, Timo ; Lewis, Cathryn M. ; Wowern, Fredrik ^LU ; Hunt, Steven ; Kardia, Sharon L.R. ; Levy, Daniel ; Perola, Markus and Rankinen, Tuomo , et al. (2004) In Human Molecular Genetics 13(19). p.2325-2332
- Contribution to journal › Article
Mark Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
Storlazzi, Clelia T ; Fioretos, Thoas ^LU ; Paulsson, Kajsa ^LU ; Strömbeck, Bodil ^LU ; Lassen, Carin ^LU ; Ahlgren, Tomas ; Juliusson, Gunnar ^LU ; Mitelman, Felix ^LU ; Rocchi, Mariano and Johansson, Bertil ^LU (2004) In Human Molecular Genetics 13(14). p.1479-1485
- Contribution to journal › Article
Mark Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice.
Gawlik, Kinga ^LU ; Miyagoe-Suzuki, Yuko ; Ekblom, Peter ^LU ; Takeda, Shin'ichi and Durbeej-Hjalt, Madeleine ^LU (2004) In Human Molecular Genetics 13(16). p.1775-1784
- Contribution to journal › Article
2003
Mark Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease
Bomprezzi, R ; Ringnér, Markus ^LU ; Kim, S ; Bittner, ML ; Khan, J ; Chen, YD ; Elkahloun, A ; Yu, AM ; Bielekova, B and Meltzer, PS , et al. (2003) In Human Molecular Genetics 12(17). p.2191-2199
- Contribution to journal › Article
Mark A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
Demenais, Florence ; Kanninen, Timo ; Lindgren, Cecilia ^LU ; Wiltshire, Steven ; Gaget, Stéphane ; Dandrieux, Candice ; Almgren, Peter ^LU ; Sjögren, Marketa ^LU ; Hattersley, Andrew and Dina, Christian , et al. (2003) In Human Molecular Genetics 12(15). p.1865-1873
- Contribution to journal › Article

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