Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Joanne M.A. Meerabux"'
Autor:
Takeo Yoshikawa, Yoshimi Iwayama, Hisako Ohba, Sevilla D. Detera-Wadleigh, Motoko Maekawa, Lynn E. DeLisi, Joanne M.A. Meerabux
Publikováno v:
Journal of Human Genetics. 54:386-391
It is suggested that chromosome 18p11 is a susceptibility region for both bipolar disorder and schizophrenia. Aiming to identify susceptibility gene(s), we investigated a family whose members have either schizophrenia or schizophrenia-spectrum psycho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37bb9b4390b2f18265609182c95be12d
https://doi.org/10.1038/jhg.2009.47
https://doi.org/10.1038/jhg.2009.47
Autor:
Yoshimi Iwayama, Kiyoshi Yoshitsugu, Tomoko Toyota, Ruby Nagata, Takeo Yoshikawa, Hiromitsu Shimizu, Kazuo Yamada, Takeshi Sakurai, Joanne M.A. Meerabux, Katsuya Ohta, Yoko Irukayama-Tomobe, Hisako Ohba
Publikováno v:
Biological Psychiatry. 58:401-407
Background Primary polydipsia is a common complication in patients with chronic psychoses, particularly schizophrenia. Disease pathogenesis is poorly understood, but one contributory factor is thought to be dopamine dysregulation caused by prolonged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45b00417ff97accacdafd201c61c7d24
https://doi.org/10.1016/j.biopsych.2005.04.015
https://doi.org/10.1016/j.biopsych.2005.04.015
Autor:
Yoshimi Iwayama-Shigeno, Yoshio Minabe, Norio Mori, Tomoko Toyota, Toshio Inada, Takeo Yoshikawa, Joanne M.A. Meerabux, Kazuo Yamada, Masanari Itokawa
Publikováno v:
Neuroscience Letters. 378:102-105
Dysfunction of the N-methyl-D-aspartate (NMDA) type glutamate receptor has been proposed as a mechanism in the etiology of schizophrenia. Recently, we identified a variable (GT)n repeat in the promoter region of the NMDA NR2A subunit gene (GRIN2A), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d014a830ef884b11975d65ca1499e5d4
https://doi.org/10.1016/j.neulet.2004.12.013
https://doi.org/10.1016/j.neulet.2004.12.013
Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B
Autor:
Masanari Itokawa, Hiromitsu Shimizu, Mitsuru Ebihara, Katsuaki Suzuki, Takeo Yoshikawa, Tomoko Toyota, Masayuki Fukasawa, Noriyoshi Takei, Kazuhiko Nakamura, Eiji Hattori, Yoshimi Iwayama-Shigeno, Hisako Ohba, Joanne M.A. Meerabux, Yoshio Minabe, Kazuo Yamada, Yoshiro Tomaru, Norio Mori, Yoshimoto Sekine, Kiyoshi Yoshitsugu
Publikováno v:
Human Molecular Genetics. 13:551-561
The increased incidence of minor physical anomalies (MPAs) in schizophrenia is the fundamental basis for the neurodevelopmental hypothesis of schizophrenia etiology. Ocular misalignment, or strabismus, falls into the category of MPAs, but this phenot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79b7f3ab904f23e9c8da287b6206cca2
https://doi.org/10.1093/hmg/ddh047
https://doi.org/10.1093/hmg/ddh047
Publikováno v:
American Journal of Medical Genetics. :27-31
We report on a male schizophrenic patient who carried an isodicentric Y chromosome [idic(Y)] with a mosaic karyotype [mos 45,X/46,X,idic(Y)(q11)]. Although a potential association between sex chromosome abnormalities and a susceptibility to psychoses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5218dbfc75ce6f74300758509f18140f
https://doi.org/10.1002/ajmg.b.10794
https://doi.org/10.1002/ajmg.b.10794
Autor:
Koji Saito, Joanne M.A. Meerabux, Tomoko Toyota, Haruo Shibuya, Takeo Yoshikawa, Kazuo Yamada, Masahiro Nankai, Eiji Hattori
Publikováno v:
American Journal of Medical Genetics. 114:84-92
Chromosome 16p13 has been shown to display modest linkage signals for mood disorders in a number of studies. An interesting candidate gene in this region is the adenylate cyclase (AC) type 9 gene (ADCY9). ACs are critical in neuronal signaling, and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36340d5af400a63e8dd04dedba145db9
https://doi.org/10.1002/ajmg.10117
https://doi.org/10.1002/ajmg.10117
Autor:
Shigeyoshi Itohara, Hisako Ohba, Yumiko Suto, Toshiaki Nakashiba, Mika Aoki-Suzuki, Sachiko Nishimura, Joanne M.A. Meerabux, Masayuki Fukasawa, Takeo Yoshikawa
Publikováno v:
Genomics. 86(1)
The recently identified netrins-G1 and -G2 form a distinct subgroup within the UNC-6/netrin gene family of axon guidance molecules. In this study, we determined the size and structure of the exon/intron layout of the human netrin-G1 (NTNG1) and -G2 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bc98820a528fa8c4ad04ef8dbcc2fcc
https://pubmed.ncbi.nlm.nih.gov/15901489
https://pubmed.ncbi.nlm.nih.gov/15901489
Autor:
Kenjiro Seki, Kazuya Iwamoto, Kazuo Yamada, Takeo Yoshikawa, Joanne M.A. Meerabux, Tadafumi Kato, Sachiko Nishimura, Mika Aoki-Suzuki, Hisako Ohba, Hitomi Takao, Yoshimi Iwayama-Shigeno, Noriaki Nakatani, Brian Dean, Shigeyoshi Itohara, Yumiko Suto, Toru Nishikawa, Tomoko Toyota
Publikováno v:
Biological psychiatry. 57(4)
Background The netrin-G1 ( NTNG1 ) and -G2 ( NTNG2 ) genes, recently cloned from mouse, play a role in the formation and/or maintenance of glutamatergic neural circuitry. Accumulating evidence strongly suggests that disturbances of neuronal developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8efbbd967fc17e056199df5e0e7e1949
https://pubmed.ncbi.nlm.nih.gov/15705354
https://pubmed.ncbi.nlm.nih.gov/15705354
Autor:
Kazuo Yamada, Eiji Hattori, Kiyoshi Yoshitsugu, Tomoko Toyota, Joanne M.A. Meerabux, Takeo Yoshikawa, Tetsuya Ichimiya, Hiromitsu Shimizu
Publikováno v:
Schizophrenia research. 52(3)
Chromosomal aberrations have long been studied in an effort to identify susceptibility genes in schizophrenia. The two most frequently detected abnormalities are X chromosome mosaicism in female patients and pericentric inversions of chromosome 9 [in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8b54ab311f7229a373cbf10e882e265
https://pubmed.ncbi.nlm.nih.gov/11705711
https://pubmed.ncbi.nlm.nih.gov/11705711