Zobrazeno 1 - 10 of 664 pro vyhledávání: '"Kazuo Nakajima"'
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Akademický článek
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice
Autor: Kazuo Nakajima, Alannah Miranda, David W. Craig, Tatyana Shekhtman, Stanislav Kmoch, Anthony Bleyer, Szabolcs Szelinger, Tadafumi Kato, John R. Kelsoe
Publikováno v: Translational Psychiatry, Vol 10, Iss 1, Pp 1-13 (2020)
Abstract Previously, we reported a family in which bipolar disorder (BD) co-segregates with a Mendelian kidney disorder linked to 1q22. The causative renal gene was later identified as MUC1. Genome-wide linkage analysis of BD in the family yielded a
Externí odkaz: https://doaj.org/article/f27b9e1bb83e49ca84843cea95c47723
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2
Akademický článek
De novo UNC13B mutation identified in a bipolar disorder patient increases a rare exon‐skipping variant
Autor: Takumi Nakamura, Kotori Jimbo, Kazuo Nakajima, Takashi Tsuboi, Tadafumi Kato
Publikováno v: Neuropsychopharmacology Reports, Vol 38, Iss 4, Pp 210-213 (2018)
Abstract Aim We previously performed the first trio‐based exome study for bipolar disorder and identified 71 de novo mutations. Among these mutations, the only mutation located at the splice donor site was in UNC13B. We focused on and analyzed the
Externí odkaz: https://doaj.org/article/9b90dd3ca84c42dca2dff3b5cc851a38
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3
Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier’s disease, causes behavioral abnormalities and a hyper-dopaminergic state
Autor: Hirotaka Shoji, Tadafumi Kato, Hiromu Monai, Tsuyoshi Miyakawa, Kazuo Nakajima, Thomas J. McHugh, Kazuhiro Yamakawa, Hiroyuki Miyamoto, Mizuho Ishiwata, Adam Z. Weitemier
Publikováno v: Human Molecular Genetics
A report of a family of Darier’s disease with mood disorders drew attention when the causative gene was identified as ATP2A2 (or SERCA2), which encodes a Ca2+ pump on the endoplasmic reticulum (ER) membrane and is important for intracellular Ca2+ s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29a65d70e5682b9168f8b34d3f66a14a
https://doi.org/10.1093/hmg/ddab137
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7
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice
Autor: Szabolcs Szelinger, Anthony J. Bleyer, Stanislav Kmoch, Kazuo Nakajima, Tatyana Shekhtman, Alannah Miranda, John R. Kelsoe, David Craig, Tadafumi Kato
Publikováno v: Translational Psychiatry, Vol 10, Iss 1, Pp 1-13 (2020)
Translational psychiatry, vol 10, iss 1
Translational Psychiatry
Previously, we reported a family in which bipolar disorder (BD) co-segregates with a Mendelian kidney disorder linked to 1q22. The causative renal gene was later identified as MUC1. Genome-wide linkage analysis of BD in the family yielded a peak at 1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85ecf72b299cbe2dc51810b2c09c1b93
https://doaj.org/article/f27b9e1bb83e49ca84843cea95c47723
Zobrazit plný text záznamu

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