نتایج جستجو برای: tgfbr2

تعداد نتایج: 564  

Journal: :Journal of biochemistry and molecular biology 2007
Na Kyung Ryu Moon Hee Yang Min Seok Jung Jeong Ok Jeon Kee Won Kim Jong Hoon Park

Methamphetamine is an illicit drug that is often abused and can cause neuropsychiatric and neurotoxic damage. Repeated administration of psychostimulants such as methamphetamine induces a behavioral sensitization. According to a previous study, Bax was involved in neurotoxicity by methamphetamine, but the function of Bax in rewarding effect has not yet been elucidated. Therefore, we have studie...

Journal: :The Turkish journal of pediatrics 2012
Esra Kiliç Yasemin Alanay Eda Utine Burçe Ozgen-Mocan Peter N Robinson Koray Boduroğlu

We report a 13-year-old girl with Loeys-Dietz syndrome (LDS) caused by a known transforming growth factor beta receptor II (TGFBR2) gene mutation, who developed aortic root dilatation and saccular aneurysm of the internal carotid artery. LDS is a rare, autosomal dominant aortic aneurysm syndrome with multisystem involvement. The disease is typically characterized by the triad of arterial tortuo...

2011
Alain C. Borczuk Marieta Sole Ping Lu Jinli Chen May-Lin Wilgus Richard A. Friedman Steven M. Albelda Charles A. Powell

Clinical investigations have suggested that repression of the TGF-b type II receptor (TbRII) may be an important step in progression of lung adenocarcinoma from an indolent in situ state to a frank invasive carcinoma. To test this hypothesis, we compared the effects of deleting the murine homolog of this receptor (Tgfbr2) in a mouse model of mutant K-ras–induced lung carcinoma, which normally i...

2017
Margot A. Cousin Michael T. Zimmermann Angela J. Mathison Patrick R. Blackburn Nicole J. Boczek Gavin R. Oliver Gwen A. Lomberk Raul A. Urrutia David R. Deyle Eric W. Klee

TGF-β-related heritable connective tissue disorders are characterized by a similar pattern of cardiovascular defects, including aortic root dilatation, mitral valve prolapse, vascular aneurysms, and vascular dissections and exhibit incomplete penetrance and variable expressivity. Because of the phenotypic overlap of these disorders, panel-based genetic testing is frequently used to confirm the ...

2014
Maria Meira Claudia Sievers Francine Hoffmann Maria Rasenack Jens Kuhle Tobias Derfuss Ludwig Kappos Raija L P Lindberg

MicroRNAs (miRNAs) are a family of noncoding RNAs that play critical roles in the posttranscriptional regulation of gene expression. Accumulating evidence supports their involvement in the pathogenesis of multiple sclerosis (MS). Here, we compare miR-17 expressions in CD4+ T cells from relapsing-remitting (RR) MS patients treated with natalizumab versus untreated patients. miR-17 was downregula...

Journal: :Development 2013
Jun-ichi Iwata Akiko Suzuki Richard C Pelikan Thach-Vu Ho Pedro A Sanchez-Lara Mark Urata Michael J Dixon Yang Chai

Cleft palate is one of the most common human birth defects and is associated with multiple genetic and environmental risk factors. Although mutations in the genes encoding transforming growth factor beta (TGFβ) signaling molecules and interferon regulatory factor 6 (Irf6) have been identified as genetic risk factors for cleft palate, little is known about the relationship between TGFβ signaling...

2014
Heather A. McCauley Chia-Yang Liu Aria C. Attia Kathryn A. Wikenheiser-Brokamp Yujin Zhang Jeffrey A. Whitsett

The ocular surface epithelia, including the stratified but nonkeratinized corneal, limbal and conjunctival epithelium, in concert with the epidermal keratinized eyelid epithelium, function together to maintain eye health and vision. Abnormalities in cellular proliferation or differentiation in any of these surface epithelia are central in the pathogenesis of many ocular surface disorders. Goble...

Journal: :Molecular pathology : MP 2001
A J Alvi J S Rader M Broggini F Latif E R Maher

AIMS To investigate the possible role of mutations in the transforming growth factor beta receptor type II gene (TGFBRII) in ovarian cancer and its relation to microsatellite instability (MSI), 43 sporadic ovarian tumours were analysed for mutations over the entire coding region of the TGFBRII gene. METHODS Mutational analysis was performed using the polymerase chain reaction (PCR), single st...

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