نتایج جستجو برای: dtnbp1

تعداد نتایج: 174  

2011
Naomi Nihonmatsu-Kikuchi Ryota Hashimoto Satoko Hattori Shinsuke Matsuzaki Takiko Shinozaki Haruka Miura Shigeru Ohota Masaya Tohyama Masatoshi Takeda Yoshitaka Tatebayashi

Genetic variations in the gene encoding dysbindin has consistently been associated with schizophrenia and bipolar disorder, although little is known about the neural functions carried out by dysbindin. To gain some insight into this area, we took advantage of the readily available dysbindin-null mouse sandy (sdy-/-) and studied hippocampal neurogenesis using thymidine analogue bromodeoxuridine ...

2015
Krzysztof P Lubieniecki Song Lin Emily I Cabana Jieying Li Yvonne Y Y Lai William S Davidson

Atlantic salmon and rainbow trout, like other members of the subfamily Salmoninae, are gonochoristic with male heterogamety. The finding that sex-linked genetic markers varied between species suggested that the sex-determining gene differs among salmonid species, or that there is one sex-determining gene that has the capacity to move around the genome. The discovery of sdY, the sex-determining ...

2011
Katsunori Kobayashi Satomi Umeda-Yano Hidenaga Yamamori Masatoshi Takeda Hidenori Suzuki Ryota Hashimoto

Dysbindin-1 (dystrobrevin-binding protein 1, DTNBP1) is one of the promising schizophrenia susceptibility genes. Dysbindin protein is abundantly expressed in synaptic regions of the hippocampus, including the terminal field of the mossy fibers, and this hippocampal expression of dysbindin is strongly reduced in patients with schizophrenia. In the present study, we examined the functional role o...

Journal: :American journal of human genetics 2005
M Daniele Fallin Virginia K Lasseter Dimitrios Avramopoulos Kristin K Nicodemus Paula S Wolyniec John A McGrath Gary Steel Gerald Nestadt Kung-Yee Liang Richard L Huganir David Valle Ann E Pulver

Bipolar, schizophrenia, and schizoaffective disorders are common, highly heritable psychiatric disorders, for which familial coaggregation, as well as epidemiological and genetic evidence, suggests overlapping etiologies. No definitive susceptibility genes have yet been identified for any of these disorders. Genetic heterogeneity, combined with phenotypic imprecision and poor marker coverage, h...

Journal: :Physiological genomics 2010
Dessie Salilew-Wondim Michael Hölker Franca Rings Nasser Ghanem Mehmet Ulas-Cinar Jaana Peippo Ernst Tholen Christian Looft Karl Schellander Dawit Tesfaye

Aberrant gene expression in the uterine endometrium and embryo has been the major causes of pregnancy failure in cattle. However, selecting cows having adequate endometrial receptivity and embryos of better developmental competence based on the gene expression pattern has been a greater challenge. To investigate whether pretransfer endometrial and embryo gene expression pattern has a direct rel...

Journal: :The international journal of neuropsychopharmacology 2007
Tadafumi Kato

At the beginning of the 20th century, when neuropathologists had long searched without success for the neural basis of schizophrenia, this field was called a ‘graveyard for neuropathologists ’. This disappointment opened the door for psychiatrists to focus on psychopathology. The discovery of antipsychotic agents in the 1950s provided a clue to understanding the pathology of this difficult dise...

Journal: :The Biochemical journal 2006
Ramin Nazarian Marta Starcevic Melissa J Spencer Esteban C Dell'Angelica

Dysbindin was identified as a dystrobrevin-binding protein potentially involved in the pathogenesis of muscular dystrophy. Subsequently, genetic studies have implicated variants of the human dysbindin-encoding gene, DTNBP1, in the pathogeneses of Hermansky-Pudlak syndrome and schizophrenia. The protein is a stable component of a multisubunit complex termed BLOC-1 (biogenesis of lysosome-related...

Journal: :Psychological medicine 2012
A L Collins Y Kim P Sklar M C O'Donovan P F Sullivan

BACKGROUND Candidate gene studies have been a key approach to the genetics of schizophrenia (SCZ). However, the results of these studies are confusing and no genes have been unequivocally implicated. The hypothesis-driven candidate gene literature can be appraised by comparison with the results of genome-wide association studies (GWAS). METHOD We describe the characteristics of hypothesis-dri...

Journal: :Schizophrenia bulletin 2007
Christopher J Carter

Bipolar disorder and schizophrenia share common chromosomal susceptibility loci and many risk-promoting genes. Oligodendrocyte cell loss and hypomyelination are common to both diseases. A number of environmental risk factors including famine, viral infection, and prenatal or childhood stress may also predispose to schizophrenia or bipolar disorder. In cells, related stressors (starvation, virus...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید