Coffee, Genetic Variants, and Parkinson's Disease: Gene–Environment Interactions

Por Yamada-Fowler, Naomi, Söderkvist, Peter
Publicado no J Caffeine Res (2015)

Caffeine Interaction with Glutamate Receptor Gene GRIN2A: Parkinson's Disease in Swedish Population

Por Yamada-Fowler, Naomi, Fredrikson, Mats, Söderkvist, Peter
Publicado em 2014

Bcl11b mutations identified in murine lymphomas increase the proliferation rate of hematopoietic progenitor cells

Por Karlsson, Anneli, Nordigården, Amanda, Jönsson, Jan-Ingvar, Söderkvist, Peter
Publicado em 2007

The Notch-2 Gene Is Regulated by Wnt Signaling in Cultured Colorectal Cancer Cells

Por Ungerbäck, Jonas, Elander, Nils, Grünberg, John, Sigvardsson, Mikael, Söderkvist, Peter
Publicado em 2011

MDM2 SNP309 promoter polymorphism and p53 mutations in urinary bladder carcinoma stage T1

Por Olsson, Hans, Hultman, Per, Rosell, Johan, Söderkvist, Peter, Jahnson, Staffan
Publicado em 2013

Activating FGFR1 Mutations in Sporadic Pheochromocytomas

Por Welander, Jenny, Łysiak, Małgorzata, Brauckhoff, Michael, Brunaud, Laurent, Söderkvist, Peter, Gimm, Oliver
Publicado no World J Surg (2017)

Polymorphisms of GSTT1, GSTM1, and EPHX genotypes in patients with cryptogenic polyneuropathy: a case–control study

Por Lindh, Jonas, Söderkvist, Peter, Fredrikson, Mats, Hosseininia, Shahrzad, Tondel, Martin, Persson, Bodil, Vrethem, Magnus
Publicado em 2011

Alterations of INPP4B, PIK3CA and pAkt of the PI3K pathway are associated with squamous cell carcinoma of the lung

Por Stjernström, Annika, Karlsson, Christina, Fernandez, Oswaldo J, Söderkvist, Peter, Karlsson, Mats G, Thunell, Lena K
Publicado em 2014

Genome-Wide Association Study to Identify Genes Related to Renal Mercury Concentrations in Mice

Por Alkaissi, Hammoudi, Ekstrand, Jimmy, Jawad, Aksa, Nielsen, Jesper Bo, Havarinasab, Said, Soderkvist, Peter, Hultman, Per
Publicado no Environ Health Perspect (2016)

A High Frequency of Sequence Alterations Is Due to Formalin Fixation of Archival Specimens

Por Williams, Cecilia, Pontén, Fredrik, Moberg, Catherine, Söderkvist, Peter, Uhlén, Mathias, Pontén, Jan, Sitbon, Gisela, Lundeberg, Joakim
Publicado em 1999

Human Gene Variants Linked to Enhanced NLRP3 Activity Limit Intramacrophage Growth of Mycobacterium tuberculosis

Por Eklund, Daniel, Welin, Amanda, Andersson, Henrik, Verma, Deepti, Söderkvist, Peter, Stendahl, Olle, Särndahl, Eva, Lerm, Maria
Publicado em 2014

The Q705K Polymorphism in NLRP3 Is a Gain-of-Function Alteration Leading to Excessive Interleukin-1β and IL-18 Production

Por Verma, Deepti, Särndahl, Eva, Andersson, Henrik, Eriksson, Per, Fredrikson, Mats, Jönsson, Jan-Ingvar, Lerm, Maria, Söderkvist, Peter
Publicado em 2012

NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients

Por Willander, Kerstin, Dutta, Ravi Kumar, Ungerbäck, Jonas, Gunnarsson, Rebeqa, Juliusson, Gunnar, Fredrikson, Mats, Linderholm, Mats, Söderkvist, Peter
Publicado em 2013

Mutations in the isocitrate dehydrogenase 2 gene and IDH1 SNP 105C > T have a prognostic value in acute myeloid leukemia

Por Willander, Kerstin, Falk, Ingrid Jakobsen, Chaireti, Roza, Paul, Esbjörn, Hermansson, Monica, Gréen, Henrik, Lotfi, Kourosh, Söderkvist, Peter
Publicado em 2014

HRAS mutation prevalence and associated expression patterns in pheochromocytoma

Por Stenman, Adam, Welander, Jenny, Gustavsson, Ida, Brunaud, Laurent, Bäckdahl, Martin, Söderkvist, Peter, Gimm, Oliver, Juhlin, C. Christofer, Larsson, Catharina
Publicado no Genes Chromosomes Cancer (2016)

Association between TERT promoter polymorphisms and acute myeloid leukemia risk and prognosis

Por Mosrati, Mohamed Ali, Willander, Kerstin, Falk, Ingrid Jakobsen, Hermanson, Monica, Höglund, Martin, Stockelberg, Dick, Wei, Yuan, Lotfi, Kourosh, Söderkvist, Peter
Publicado no Oncotarget (2015)

Rare Germline Mutations Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma

Por Welander, Jenny, Andreasson, Adam, Juhlin, C. Christofer, Wiseman, Roger W., Bäckdahl, Martin, Höög, Anders, Larsson, Catharina, Gimm, Oliver, Söderkvist, Peter
Publicado no J Clin Endocrinol Metab (2014)

Common Genetic Variations in the NALP3 Inflammasome Are Associated with Delayed Apoptosis of Human Neutrophils

Por Blomgran, Robert, Patcha Brodin, Veronika, Verma, Deepti, Bergström, Ida, Söderkvist, Peter, Sjöwall, Christopher, Eriksson, Per, Lerm, Maria, Stendahl, Olle, Särndahl, Eva
Publicado em 2012

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

Por Hmani-Aifa, Mounira, Benzina, Zeineb, Zulfiqar, Fareeha, Dhouib, Houria, Shahzadi, Amber, Ghorbel, Abdelmonem, Rebaï, Ahmed, Söderkvist, Peter, Riazuddin, Sheikh, Kimberling, William J, Ayadi, Hammadi
Publicado em 2009

TERT promoter mutations and polymorphisms as prognostic factors in primary glioblastoma

Por Mosrati, Mohamed Ali, Malmström, Annika, Lysiak, Malgorzata, Krysztofiak, Adam, Hallbeck, Martin, Milos, Peter, Hallbeck, Anna-Lotta, Bratthäll, Charlotte, Strandéus, Michael, Stenmark-Askmalm, Marie, Söderkvist, Peter
Publicado no Oncotarget (2015)