Zobrazeno 1 - 10
of 163
pro vyhledávání: '"Maria Anvret"'
Autor:
Passarge, Eberhard
Publikováno v:
The Quarterly Review of Biology, 1994 Dec 01. 69(4), 556-557.
Externí odkaz:
https://www.jstor.org/stable/3036522
Autor:
Eberhard Passarge
Publikováno v:
The Quarterly Review of Biology. 69:556-557
Publikováno v:
Neurobiology of Disease, Vol 14, Iss 3, Pp 637-647 (2003)
Dopamine (DA) neurons degenerate in Parkinson's disease and dopamine neurotransmission may be affected in psychotic states seen in schizophrenia. Understanding the regulation of enzymes involved in DA metabolism may therefore lead to new treatment st
Externí odkaz:
https://doaj.org/article/890c41e62ff544788d74475b1bb80e5d
Autor:
Anna Håkansson, Olof Sydow, Andrea Carmine Belin, Peter Söderkvist, Marie Westerlund, Thomas Willows, Anna Anvret, Hans Nissbrandt, Silvia Paddock, Caroline Ran, Ahmad Ahmadi, Dagmar Galter, Maria Anvret, Nil Dizdar
Publikováno v:
Neuroscience Letters. 522:30-35
Pesticide exposure has been suggested to increase the risk to develop Parkinson's disease (PD). The arylesterase paraoxonase 1 (PON1) is mainly expressed in the liver and hydrolyzes organophosphates such as pesticides. The polymorphism Leu54Met (rs85
Autor:
Bengt Winblad, Maria Anvret, Conneally M, Hobbs W, Gösta Holmgren, Almqvist Ew, Jan Wahlström, Bengt Mattsson, James F. Gusella
Publikováno v:
Clinical Genetics. 32:289-294
Two Swedish families with Huntington's disease (HD) have been investigated for linkage with G8 (D4S10). In one family from northern Sweden (Family 1) 48 family members were examined, and in another family from the southwestern part of Sweden (Family
Publikováno v:
Neurogenetics. 4:173-177
Welander distal myopathy (WDM) is a late adult-onset autosomal dominant disorder, characterized by a slow progression and distal limb weakness of the extremity muscles. The WDM locus has been mapped to chromosome 2p13. Within this region a common sha
Autor:
Silvia Buervenich, Maria Anvret, Göran Sedvall, Andrea Carmine, Olof Sydow, J. Petter Gustavsson, Hans Bergman, Dagmar Galter, Kodavali V. Chowdari, Erik G. Jönsson, Lars Olson, Lars Farde, Vishwajit L. Nimgaonkar
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :51-57
We have previously identified mutations in exon three in NURR1 (NR4A2) in two patients with schizophrenia (SZ) and one patient with bipolar disease with psychotic symptoms. In the present study we analyzed the promoter region of NURR1 and identified
Autor:
Lars Farde, Hans Bergman, Erik G. Jönsson, Maria Anvret, Milan G. Chheda, Göran Sedvall, Andrea Carmine, J. P. Gustavsson, Silvia Buervenich, Lars Olson
Publikováno v:
Psychiatric Genetics. 13:23-28
BACKGROUND Recently, linkage disequilibrium mapping of the major histocompatibility complex region on the short arm of human chromosome 6 suggested that the NOTCH4 locus is highly associated with schizophrenia. OBJECTIVES AND METHODS We analysed two
Autor:
L Lilius, Maria Anvret, Dennis Hellgren, Jan Hillert, Hugh Salter, Zhiping Zhang, Lars Lannfelt, Thomas Masterman
Publikováno v:
Multiple Sclerosis Journal. 8:98-103
Apolipoprotein E (opoE) is involved in the transport of lipids necessary for membrane repair and is encoded by a gene on chromosome 19q13, a region positive for linkage in two multiple sclerosis (MS) genome-wide screens. The APOE epsilon4 allele conf
Publikováno v:
Movement Disorders. 15:813-818
Mutations in alcohol dehydrogenase (ADH; EC 1.1.1.1) genes may be of interest in the etiology of Parkinson's disease (PD) because of the important role these enzymes play in retinoid and dopamine metabolism and/or aldehyde detoxification. The locatio