Zobrazeno 1 - 10
of 31
pro vyhledávání: '"M. Horie"'
Autor:
Tomohito Saito, Christian P Houbois, Shaf Keshavjee, Kristy K. Brock, Shailaja Sajja, Pascal Salazar, Tereza Martinu, Ciara OʼBrien, Kazuhiro Yasufuku, Narinder Paul, Mini Pakkal, M. Horie, Liran Levy
Publikováno v:
Transplantation. 103:2645-2653
Background Chronic lung allograft dysfunction (CLAD) limits long-term survival after lung transplantation (LTx). Early detection or prediction of CLAD can lead to changes in patient management that, in turn, may improve prognosis. The purpose of this
Autor:
David M. Hwang, Betty Joe, Andrzej Chruscinski, Tatsuaki Watanabe, M. Horie, Z. Guan, Ke Fan Bei, Mingyao Liu, K. Boonstra, Tereza Martinu, Shaf Keshavjee, Stephen C. Juvet
Publikováno v:
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant SurgeonsREFERENCES. 19(12)
Chronic lung allograft dysfunction (CLAD) limits long-term survival after lung transplant (LT). Ischemia-reperfusion injury (IRI) promotes chronic rejection (CR) and CLAD, but the underlying mechanisms are not well understood. To examine mechanisms l
Autor:
Kristy K. Brock, Pascal Salazar, Luigia D'Errico, Matthew Binnie, Tomohito Saito, D. Nakajima, Narinder Paul, M. Horie, Kazuhiro Yasufuku, Shaf Keshavjee, Joanne Moseley
Publikováno v:
Clinical transplantation. 31(8)
Chronic lung allograft dysfunction (CLAD) reduces long-term graft survival. It is important to distinguish CLAD subtypes: bronchiolitis obliterans syndrome (BOS) and restrictive allograft syndrome (RAS) as RAS has a worse prognosis and accurate subty
Autor:
Pascal Salazar, Matthew Binnie, Narinder Paul, Tereza Martinu, Tomohito Saito, Sassan Azad, Shaf Keshavjee, Kristy K. Brock, M. Horie, Kazuhiro Yasufuku
Publikováno v:
Clinical Transplantation. 32:e13233
Chronic lung allograft dysfunction (CLAD) is a major cause of mortality in lung transplant recipients. CLAD can be sub-divided into at least 2 subtypes with distinct mortality risk characteristics: restrictive allograft syndrome (RAS), which demonstr
Autor:
Tomohito Saito, David M. Hwang, Marcelo Cypel, Matthew Binnie, Tiago N. Machuca, M. Horie, Lianne G. Singer, Thomas K. Waddell, Hassan Shoushtarizadeh, Masaaki Sato, Mingyao Liu, Daisuke Nakajima, Sassan Azad, Narinder Paul, Shaf Keshavjee
Publikováno v:
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 35(1)
The long-term success of lung transplantation is challenged by the development of chronic lung allograft dysfunction (CLAD) and its distinct subtypes of bronchiolitis obliterans syndrome (BOS) and restrictive allograft syndrome (RAS). However, the cu
Publikováno v:
Clinical genetics. 87(3)
Andersen-Tawil syndrome (ATS) is an inherited disease characterized by ventricular arrhythmias, periodic paralysis, and dysmorphic features. It results from a heterozygous mutation of KCNJ2, but little is known about mosaicism in ATS. We performed ge
Publikováno v:
Cytogenetic and Genome Research. 83:232-235
The ING1 gene encodes p33ING1, a putative tumor suppressor for neuroblastomas and breast cancers, which has been shown to cooperate with p53 in controlling cell proliferation. We have isolated a novel human gene, ING1L, that potentially encodes a PHD
Autor:
Seiko Ohno, Hiroshi Matsuura, Dimitar P. Zankov, Hideki Itoh, Wei-Guang Ding, Takeru Makiyama, Jules C. Hancox, Takahiro Doi, Satoshi Shizuta, M. Horie, Akashi Miyamoto, Nobu Naiki, Tetsuhisa Hattori
Publikováno v:
Circulation. Arrhythmia and electrophysiology. 4(3)
Background— Brugada syndrome (BrS) has a significantly higher incidence among the male sex. Among genes coding ion channels and their modulatory proteins, KCNE5 ( KCNE1L ) is located in the X chromosome and encodes an auxiliary β-subunit for K cha
Autor:
Takeru Makiyama, Yoshisumi Haruna, Masaharu Akao, Seiko Ohno, Keiko Tsuji, Takahiro Doi, Takeshi Morimoto, Takeshi Kimura, Yoshiaki Takahashi, M. Horie
Publikováno v:
Circulation. Cardiovascular genetics. 4(3)
Background— Mutations in KCNJ2 , a gene encoding the inward rectifier K + channel Kir2.1, are associated with Andersen-Tawil syndrome (ATS), which is characterized by (1) ventricular tachyarrhythmias associated with QT (QU)-interval prolongation, (
Publikováno v:
Archives of gynecology and obstetrics. 264(1)
A multigravida patient with polyarthralgia and eruptions on the head and fingers was seen at 6 weeks’ gestation. No histological examination was performed before the current pregnancy. She developed severe early onset preeclampsia associated with s