نتایج جستجو برای: htra1

تعداد نتایج: 528  

Journal: :Endocrinology 2011
Mark A Fenwick Yosef T Mansour Stephen Franks Kate Hardy

The TGFβ superfamily comprises several bone morphogenetic proteins (BMP) capable of exerting gonadotropin-independent effects on the development of small preantral follicles. In embryonic tissues, BMP concentration gradients, partly formed by antagonistic factors, are essential for establishing phenotypic fate. By examining the expression of candidate genes whose protein products are known to i...

2015
Kai Fang Pei Gao Jun Tian Xueying Qin Wenzhen Yu Juan Li Qing Chen Lvzhen Huang Dafang Chen Yonghua Hu Xiaoxin Li

Purpose. The etiology of neovascular age-related macular degeneration (nAMD) cannot be completely explained by identified environmental risk factors or single-locus gene variants. This study was to explore the potential interactions among gene variants on nAMD in Chinese population. Methods. 43 SNPs located in different genes were genotyped in 932 Chinese individuals (464 nAMD patients and 468 ...

Journal: :Brazilian Journal of Medical and Biological Research 2018

Journal: :Rinsho shinkeigaku = Clinical neurology 2010
Kenju Hara

Hypertension is a well known risk factor for cerebral small vessel disease (SVD) characterized by MRI white matter hyperintensities called "leukoaraiosis". However, the molecular basis of SVD remains to be elucidated. Both twin and family studies have shown that leukoaraiosis is the most heritable cerebrovascular phenotype with a heritability estimated to be between 55% and 71%, suggesting gene...

2016
David L. Kooyman

Inflammatory response and calcification are strongly implicated in osteoarthritis (OA) progression. Key inflammatory biomarkers present throughout the process of OA have been established but an association with calcification has not been clarified. A faint line, tidemark, exists between the subchondral bone and the articular surface in knee joints that is presumed to be the line of demarcation ...

Journal: :Brain Research 2016
Vincent Primo Mark Graham Alexander A. Bigger-Allen Joel M. Chick Carolina Ospina Yakeel T. Quiroz Jan Manent Steven P. Gygi Francisco Lopera Patricia A. D’Amore Joseph F. Arboleda-Velasquez

Mutations in NOTCH 3 are the cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a neurological disorder characterized by stroke, and vascular cognitive impairment and dementia. Loss of vascular smooth muscle cells (VSMC) and accumulation of granular osmiophilic material (GOM) deposits are hallmarks of CADASIL. There are no therapies fo...

Journal: :Reproductive sciences 2010
Daniel Blassioli Dentillo Juliana Meola Julio Cesar Rosa e Silva Silvana Giuliatti Wilson Araujo Silva Junior Rui Alberto Ferriani Lucia Martelli

Endometriosis is a gynecologic disease characterized by the presence of endometrial tissue outside the uterine cavity. Although 15% of the female population in reproductive age is affected by endometriosis, its pathogenesis remains unclear. According to the most accepted pathogenesis hypothesis, endometrial fragments from the menstrual phase are transported through the uterine tubes to the peri...

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