نتایج جستجو برای: gsk3b

تعداد نتایج: 241  

Journal: :Cell Death and Disease 2021

Abstract The mitochondrial DNA m.3243A > G mutation is well-known to cause a variety of clinical phenotypes, including diabetes, deafness, and osteoporosis. Here, we report isolation expansion urine-derived stem cells (USCs) from patients carrying the mutation, which demonstrate bimodal heteroplasmy. USCs with high levels displayed abnormal morphology function, as well elevated ATF5-dependen...

2017
Amanda Carr James Williamson

Nearly one in five adults in the United States experience mental illness during a year (NAMI). Neurobiological correlates of these diseases may provide treatment options if they are better understood. Research has provided evidence supporting p38’s role in many mental health disorders. P38 mitogen-activated protein kinases appear frequently in literature regarding cellular threats, such as UV i...

2011
Yuhui Jiang Xiaoduo Xie Zhigang Li Zheng Wang Yixuan Zhang Zhiqiang Ling Yi Pan Zhenzhen Wang Yan Chen

Raf kinase trapping to Golgi (RKTG) is a potential tumor suppressor gene due to its negative roles in regulating Ras/Raf/MEK/ERK (extracellular signal–regulated kinase) pathway and GPCR (G protein–coupled receptor) Gbg subunit signaling. Interestingly, RKTG-deficient mice are free of tumors, although they are prone to form skin cancer on carcinogen administration. On the other hand, p53 is a we...

2017
Gabriel Nasri Marzuca-Nassr Gilson Masahiro Murata Amanda Roque Martins Kaio Fernando Vitzel Amanda Rabello Crisma Rosângela Pavan Torres Jorge Mancini-Filho Jing Xuan Kang Rui Curi

The consequences of two-week hindlimb suspension (HS) on skeletal muscle atrophy were investigated in balanced diet-fed Fat-1 transgenic and C57BL/6 wild-type mice. Body composition and gastrocnemius fatty acid composition were measured. Skeletal muscle force, cross-sectional area (CSA), and signaling pathways associated with protein synthesis (protein kinase B, Akt; ribosomal protein S6, S6, e...

2013
Ji-Hyuk Park Hee-Young Kwon Eun Jung Sohn Kyung A Kim Bonglee Kim Soo-Jin Jeong Jun ho Song Jin Suk Koo Sung-Hoon Kim

Background: Ursolic acid, a pentacyclic triterpenoid, is known to exert antitumor activity in breast, lung, liver and colon cancers. Nonetheless, the underlying mechanism of ursolic acid in prostate cancer cells still remains unclear. To investigate the antitumor mechanism, the apoptotic mechanism of ursolic acid via Wnt/b-catenin signaling was examined in PC-3 prostate cancer cells. Methods: C...

2013
Daniel F Kripke Caroline M Nievergelt Gregory J Tranah Sarah S Murray Katharine M Rex Alexandra P Grizas Elizabeth K Hahn Heon-Jeong Lee John R Kelsoe Lawrence E Kline

BACKGROUND There are several indications that malfunctions of the circadian clock contribute to depression. To search for particular circadian gene polymorphisms associated with depression, diverse polymorphisms were genotyped in two samples covering a range of depressed volunteers and participants with normal mood. METHODS Depression mood self-ratings and DNA were collected independently fro...

2015
Yi Wen Ning Lin Hong-Tao Yan Hao Luo Guang-Yu Chen Jian-Feng Cui Li Shi Tao Chen Tao Wang Li-Jun Tang

OBJECTIVE This study was initiated to evaluate the effects of Roux-en-Y gastric bypass surgery on renal gluconeogenesis in type 2 diabetic rats and its relationship with hormonal parameters. METHODS Diabetic rats were induced by intraperitoneal injection of streptozotocin (STZ; 35 mg/kg) combined with a high-fat diet. They were then randomly divided into three groups: diabetes model group (DM...

Journal: :Human molecular genetics 2014
Atsushi Iwata Kenichi Nagata Hiroyuki Hatsuta Hiroshi Takuma Miki Bundo Kazuya Iwamoto Akira Tamaoka Shigeo Murayama Takaomi Saido Shoji Tsuji

The hallmark of Alzheimer's disease (AD) pathology is an accumulation of amyloid β (Aβ) and phosphorylated tau, which are encoded by the amyloid precursor protein (APP) and microtubule-associated protein tau (MAPT) genes, respectively. Less than 5% of all AD cases are familial in nature, i.e. caused by mutations in APP, PSEN1 or PSEN2. Almost all mutations found in them are related to an overpr...

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