Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Kiyoshi, Kawakami"'
Publikováno v:
FEBS Open Bio, Vol 10, Iss 6, Pp 1031-1043 (2020)
The ATP1A2 coding α2 subunit of Na,K‐ATPase, which is predominantly located in astrocytes, is a causative gene of familial hemiplegic migraine type 2 (FHM2). FHM2 model mice (Atp1a2tmCKwk/+) are susceptible to cortical spreading depression (CSD),
Externí odkaz:
https://doaj.org/article/3ffa051a7ab94110b181a16f7dd72830
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0246678 (2021)
Na+,K+-ATPase is a crucial protein responsible for maintaining the electrochemical gradients across the cell membrane. The Na+,K+-ATPase is comprised of catalytic α, β, and γ subunits. In adult brains, the α3 subunit, encoded by ATP1A3, is predom
Externí odkaz:
https://doaj.org/article/f4e2e527b9a44357b7d37719e1ee00b2
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 10 (2018)
Omphalocele is a human congenital anomaly in ventral body wall closure and may be caused by impaired formation of the primary abdominal wall (PAW) and/or defects in abdominal muscle development. Here, we report that mice doubly deficient in homeobox
Externí odkaz:
https://doaj.org/article/b8b9666b7f994cc49c5c3be42c5751d3
Autor:
Keiji, Nogami, Masashi, Taki, Tadashi, Matsushita, Tetsuhito, Kojima, Toshiaki, Oka, Shouichi, Ohga, Kiyoshi, Kawakami, Michio, Sakai, Takashi, Suzuki, Satoshi, Higasa, Yasuo, Horikoshi, Keiko, Shinozawa, Shogo, Tamura, Koji, Yada, Masue, Imaizumi, Yoshitoshi, Ohtsuka, Fuminori, Iwasaki, Masao, Kobayashi, Junki, Takamatsu, Hideyuki, Takedani, Hisaya, Nakadate, Yoko, Matsuo, Takeshi, Matsumoto, Teruhisa, Fujii, Katsuyuki, Fukutake, Akira, Shirahata, Akira, Yoshioka, Midori, Shima
Publikováno v:
Haemophilia : the official journal of the World Federation of HemophiliaREFERENCES. 28(5)
Inhibitor-development is a serious complication in patients with haemophilia (PwH). Previous studies reported that therapeutic and genetic factors could be associated with these alloantibodies. Relevant clinical features such as genetic-background an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::619733c6262c613c5b99a8ef1c80138a
https://pubmed.ncbi.nlm.nih.gov/35689832
https://pubmed.ncbi.nlm.nih.gov/35689832
Publikováno v:
FEBS Open Bio, Vol 10, Iss 6, Pp 1031-1043 (2020)
FEBS Open Bio
FEBS Open Bio
The ATP1A2 coding α2 subunit of Na,K‐ATPase, which is predominantly located in astrocytes, is a causative gene of familial hemiplegic migraine type 2 (FHM2). FHM2 model mice (Atp1a2tmCKwk/+) are susceptible to cortical spreading depression (CSD),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd6aa2c9fde4bba2e0937316519acf32
https://doi.org/10.1002/2211-5463.12848
https://doi.org/10.1002/2211-5463.12848
Autor:
Keiko Ikeda, Masanori Takahashi, Shigeru Sato, Hiroyuki Igarashi, Toru Ishizuka, Hiromu Yawo, Satoru Arata, E Michelle Southard-Smith, Kiyoshi Kawakami, Hiroshi Onimaru
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0132475 (2015)
The key role of the respiratory neural center is respiratory rhythm generation to maintain homeostasis through the control of arterial blood pCO2/pH and pO2 levels. The neuronal network responsible for respiratory rhythm generation in neonatal rat re
Externí odkaz:
https://doaj.org/article/a7efbc9ea2ad4d4c829582b0e34ae824
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0136666 (2015)
SIX1 homeodomain protein is one of the essential key regulators of sensory organ development. Six1-deficient mice lack the olfactory epithelium, vomeronasal organs, cochlea, vestibule and vestibuloacoustic ganglion, and also show poor neural differen
Externí odkaz:
https://doaj.org/article/5e5b6ffd82414da2a7d70709ff1c72e5
Publikováno v:
The Journal of comparative neurologyREFERENCES. 529(16)
The dorsolateral striatum (DLS) of rodents is functionally subdivided into somatotopic subregions that represent each body part along both the dorsoventral and anteroposterior (A-P) axes and play crucial roles in sensorimotor functions via corticostr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54da4cdb5baf2202f3f8a13c45adb0d2
https://pubmed.ncbi.nlm.nih.gov/34240415
https://pubmed.ncbi.nlm.nih.gov/34240415
Autor:
Masahiko Izumizaki, Kazuto Kobayashi, Keiko Ikeda, Hiroyuki Igarashi, Hiroshi Onimaru, Hiromu Yawo, Kiyoshi Kawakami, Satoru Arata
Publikováno v:
Pflügers Archiv - European Journal of Physiology. 471:1419-1439
Paired-like homeobox gene Phox2b is predominantly expressed in pre-inspiratory neurons in the parafacial respiratory group (pFRG) in newborn rat rostral ventrolateral medulla. To analyse detailed local networks of the respiratory centre using optogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dd76b9b8008252869abb751e54a8ac4
https://doi.org/10.1007/s00424-019-02317-9
https://doi.org/10.1007/s00424-019-02317-9