Zobrazeno 1 - 10
of 11
pro vyhledávání: '"J R, Kelsoe"'
Autor:
Dilip V. Jeste, J R Kelsoe
Publikováno v:
Molecular Psychiatry. 2:86-88
Schizophrenia, tardive dyskinesia, and a D3 receptor gene variant: a new twist on dyskinesias?
Autor:
T A, Greenwood, M, Alexander, P E, Keck, S, McElroy, A D, Sadovnick, R A, Remick, J R, Kelsoe
Publikováno v:
American journal of medical genetics. 105(2)
A role for the dopamine transporter (DAT) in bipolar disorder is implicated by several lines of pharmacological evidence, as well as suggestive evidence of linkage at this locus, which we have reported previously. In an attempt to identify functional
Autor:
J R, Kornberg, J L, Brown, A D, Sadovnick, R A, Remick, P E, Keck, S L, McElroy, M H, Rapaport, P M, Thompson, J B, Kaul, C M, Vrabel, S C, Schommer, T, Wilson, D, Pizzuco, S, Jameson, L, Schibuk, J R, Kelsoe
Publikováno v:
Journal of affective disorders. 59(3)
Numerous genetic mechanisms and modes of transmission underlying bipolar affective disorder (BPAD) have been postulated. Recently, the discovery of genomic imprinting and mitochondrial transmission of illness in humans has stimulated study of parent-
Publikováno v:
American journal of medical genetics. 88(4)
Evidence for a bipolar disorder (BPD) susceptibility locus on chromosome 22q11 has been provided in several studies. One candidate gene that maps to this region is the G-protein alpha subunit gene Galphaz (GNAZ). We have identified a common silent po
Autor:
H M, Lachman, J R, Kelsoe, R A, Remick, A D, Sadovnick, M H, Rapaport, M, Lin, B A, Pazur, A M, Roe, T, Saito, D F, Papolos
Publikováno v:
American journal of medical genetics. 74(2)
Velo-cardio-facial syndrome (VCFS) is a congenital anomaly characterized by multiple dysmorphisms, cleft palate, cardiac anomalies, and learning disabilities, that results from a microdeletion of chromosome 22q11. An increased prevalence of psychiatr
Autor:
J R, Kelsoe, A D, Sadovnick, H, Kristbjarnarson, P, Bergesch, Z, Mroczkowski-Parker, M, Drennan, M H, Rapaport, P, Flodman, M A, Spence, R A, Remick
Publikováno v:
American journal of medical genetics. 67(6)
The dopamine transporter (DAT) plays a key role in the regulation of dopaminergic neurotransmission by mediating the active reuptake of synaptic dopamine. It is an important candidate gene for bipolar disorder because of data implicating dopamine abn
Autor:
J R, Kelsoe, R A, Remick, A D, Sadovnick, H, Kristbjarnarson, P, Flodman, M A, Spence, M, Morison, Z, Mroczkowski-Parker, P, Bergesch, M H, Rapaport, A L, Mirow, R D, Blakely, T, Helgason, J A, Egeland
Publikováno v:
American journal of medical genetics. 67(2)
The serotonin transporter (HTT) is an important candidate gene for the genetic transmission of bipolar disorder. It is the site of action of many antidepressants, and plays a key role in the regulation of serotonin neurotransmission. Many studies of
Publikováno v:
The Journal of clinical psychiatry. 56(2)
Gender may play an important role in the etiopathophysiology of psychiatric illness and has become a subject of increasing interest because of its possible effects on biological markers, treatment outcome, and prognosis. Intrigued by this issue and a
Autor:
J R, Kelsoe
Publikováno v:
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 6(4)
Autor:
J R Kelsoe
Publikováno v:
Molecular Psychiatry. 3:475-476
The serotonin transporter has long been a focus of studies of mood disorders because of its role as a site of antidepressants. The recent cloning of the gene and identification of a functional polymorphism have fueled a new round of intriguing result