Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Yuichiro Takada"'
Autor:
Toru Noda, Atsushi Shimazaki, Setsuko Noda, Masaki Sasaoka, Takeshi Iwata, Masayoshi Minami, Yuichiro Takada, Stanislav I. Tomarev, Tetsuya Yamamoto, Masakazu Akahori, Zai-Long Chi, Naoki Nakaya, Kazuhide Kawase, Minoru Obazawa
Publikováno v:
Human Molecular Genetics
Glaucoma is one of the leading causes of bilateral blindness affecting nearly 8 million people worldwide. Glaucoma is characterized by a progressive loss of retinal ganglion cells (RGCs) and is often associated with elevated intraocular pressure (IOP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d3e0b1c8f06df481c79a5920e0e2bd
https://doi.org/10.1093/hmg/ddq146
https://doi.org/10.1093/hmg/ddq146
Autor:
Paul A. Sieving, Yuichiro Takada, Michael T. Trese, Jonathan L. Prenner, Stefano Ciaccia, Antonio Capone
Publikováno v:
Retina. 26:S61-S64
To establish a classification system for congenital X-linked retinoschisis (CXLRS) using clinical examination and optical coherence tomography (OCT).Thirty-eight eyes of 19 patients who carried a clinical diagnosis of CXLRS were examined with OCT and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3782d46761ead6b168d0a86d2cbc6f4
https://doi.org/10.1097/01.iae.0000244290.09499.c1
https://doi.org/10.1097/01.iae.0000244290.09499.c1
Autor:
Tamotsu Ichiba, Samir M. Hanash, Yoshinobu Maeda, Yuichiro Takada, James L.M. Ferrara, David E. Misek, Rork Kuick, Chen Liu, Debra L. Williams, Takanori Teshima, Pavan Reddy
Publikováno v:
Blood. 102:763-771
The liver, skin, and gastrointestinal tract are major target organs of acute graft-versus-host disease (GVHD), the major complication of allogeneic bone marrow transplantation (BMT). In order to gain a better understanding of acute GVHD in the liver,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbf9821f2e4fb47a2143230afc28d333
https://doi.org/10.1182/blood-2002-09-2748
https://doi.org/10.1182/blood-2002-09-2748
Autor:
Thomas L. Saunders, Yuichiro Takada, Prabodha K. Swain, Mineo Kondo, Ronald A. Bush, Paul A. Sieving, Anand Swaroop, Alan J. Mears
Publikováno v:
Nature Genetics. 29:447-452
The protein neural retina leucine zipper (Nrl) is a basic motif-leucine zipper transcription factor that is preferentially expressed in rod photoreceptors. It acts synergistically with Crx to regulate rhodopsin transcription. Missense mutations in hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aafe41a5b3d7a7e5ed37a8e12a04082c
https://doi.org/10.1038/ng774
https://doi.org/10.1038/ng774
Publikováno v:
Volume 4: 8th International Conference on Multibody Systems, Nonlinear Dynamics, and Control, Parts A and B.
This paper deals with a dynamic analysis of a racing kart considering an elastic deformation of the kart frame. As the first step of this research, the FEM kart frame model was validated by means of static and dynamic tests. In the static test, the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4be5d9b35385a062a28a44456b7bd036
https://doi.org/10.1115/detc2011-48019
https://doi.org/10.1115/detc2011-48019
Autor:
Tetsuhisa Hatase, Hisao Ohde, Yuichiro Takada, H. Okamoto, Takeshi Iwata, Tomoaki Usui, Yozo Miyake, Kazushige Tsunoda, Shoji Tsuji, Hiroyuki Ishiura, Masakazu Akahori, Takeshi Itabashi, Yoko Fukuda, Makoto Nakamura
Occult macular dystrophy (OMD) is an inherited macular dystrophy characterized by progressive loss of macular function but normal ophthalmoscopic appearance. Typical OMD is characterized by a central cone dysfunction leading to a loss of vision despi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b107a9a3d8b218ac88b345105cedfd67
https://europepmc.org/articles/PMC2933341/
https://europepmc.org/articles/PMC2933341/
Publikováno v:
Advances in experimental medicine and biology. 613
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::303b36584b5fa4093f7ab3d0c7883bf0
https://pubmed.ncbi.nlm.nih.gov/18188957
https://pubmed.ncbi.nlm.nih.gov/18188957
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9780387749020
Retinoschisin (RS), the product of the RS1 gene on the X-chromosome (Xp22), is a 24 kDa secreted protein which is expressed exclusively in the retina (Reid et al., 1999; Sauer et al., 1997) and pineal gland (Takada et al., 2006). In the retina, photo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d617fe40106c752520af75cb8143a95
https://doi.org/10.1007/978-0-387-74904-4_34
https://doi.org/10.1007/978-0-387-74904-4_34
Autor:
Yuichiro, Takada, Robert N, Fariss, Morten, Muller, Ronald A, Bush, Elisabeth J, Rushing, Paul A, Sieving
Publikováno v:
Molecular vision. 12
The pineal gland shares a common neuroectoderm origin with the retina, and like the retina, regulates circadian rhythms through melatonin secretion. Recent expressed tag sequence (EST) analysis showed that several gene mutations, including RS1, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::870d0cf407a6213ebc91d5610186c089
https://pubmed.ncbi.nlm.nih.gov/17093404
https://pubmed.ncbi.nlm.nih.gov/17093404
Autor:
Yong Zeng, Paul A. Sieving, Ronald A. Bush, Yuichiro Takada, Camasamudram Vijayasarathy, Mary Ann Gawinowicz
Publikováno v:
Biochemical and biophysical research communications. 349(1)
Retinoschisin (RS) is a 24 kDa secreted protein expressed in retina and is required for the structural and functional integrity of the retina. RS has been predicted to serve as an adhesive protein but the precise molecular mechanism by which it funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cfbcac4817cb59a9481194cc4bcdb30
https://pubmed.ncbi.nlm.nih.gov/16930543
https://pubmed.ncbi.nlm.nih.gov/16930543