نتایج جستجو برای: wdr12 gene

تعداد نتایج: 1141372  

2015
Anne-Mari Moilanen Jaana Rysä Leena Kaikkonen Teemu Karvonen Erja Mustonen Raisa Serpi Zoltán Szabó Olli Tenhunen Zsolt Bagyura Juha Näpänkangas Pauli Ohukainen Pasi Tavi Risto Kerkelä Margrét Leósdóttir Björn Wahlstrand Thomas Hedner Olle Melander Heikki Ruskoaho

AIMS In a recent genome-wide association study, WD-repeat domain 12 (WDR12) was associated with early-onset myocardial infarction (MI). However, the function of WDR12 in the heart is unknown. METHODS AND RESULTS We characterized cardiac expression of WDR12, used adenovirus-mediated WDR12 gene delivery to examine effects of WDR12 on left ventricular (LV) remodeling, and analyzed relationship b...

Journal: :international journal of molecular and cellular medicine 0
mohammad piryaei department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) sayyed mohammad hossein ghaderian department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) hossein vakili cardiovascular research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) hooshang zaimkohan department of medical genetics, faculty of medicine, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) nastaran mohammadi ghahhari department of biochemistry, pasteur institute of iran, tehran, iran.سازمان اصلی تایید شده: انستیتو پاستور ایران (pasteur institute of iran) maryam mafi golchin department of genetics and anatomy, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences)

although genetic variants that affect susceptibility to coronary artery disease (cad) have been greatly known, a number of these single nucleotide polymorphisms (snps) remain to be analyzed in populations with different ethnicities. cad is influenced by numerous genetic, environmental, and lifestyle factors, and is an important reason for mortality around the globe. in this study, a novel snp (...

Journal: :The Journal of Cell Biology 2005
Michael Hölzel Michaela Rohrmoser Martin Schlee Thomas Grimm Thomas Harasim Anastassia Malamoussi Anita Gruber-Eber Elisabeth Kremmer Wolfgang Hiddemann Georg W. Bornkamm Dirk Eick

Target genes of the protooncogene c-myc are implicated in cell cycle and growth control, yet the linkage of both is still unexplored. Here, we show that the products of the nucleolar target genes Pes1 and Bop1 form a stable complex with a novel member, WDR12 (PeBoW complex). Endogenous WDR12, a WD40 repeat protein, is crucial for processing of the 32S precursor ribosomal RNA (rRNA) and cell pro...

2016
Chang Sook Ahn Hui Kyung Cho Du-Hwa Lee Hee-Jung Sim Sang-Gyu Kim Hyun-Sook Pai

The nucleolar protein pescadillo (PES) controls biogenesis of the 60S ribosomal subunit through functional interactions with Block of Proliferation 1 (BOP1) and WD Repeat Domain 12 (WDR12) in plants. In this study, we determined protein characteristics and in planta functions of BOP1 and WDR12, and characterized defects in plant cell growth and proliferation caused by a deficiency of PeBoW (PES...

Journal: :Nucleic Acids Research 2006
Thomas Grimm Michael Hölzel Michaela Rohrmoser Thomas Harasim Anastassia Malamoussi Anita Gruber-Eber Elisabeth Kremmer Dirk Eick

The nucleolar PeBoW-complex, consisting of Pes1, Bop1 and WDR12, is essential for cell proliferation and processing of ribosomal RNA in mammalian cells. Here we have analysed the physical and functional interactions of Pes1 deletion mutants with the PeBoW-complex. Pes1 mutants M1 and M5, with N- and C-terminal truncations, respectively, displayed a dominant-negative phenotype. Both mutants show...

2015
Mohammad Piryaei Sayyed Mohammad Hossein Ghaderian Hossein Vakili Hooshang Zaimkohan Nastaran Mohammadi Ghahhari Maryam Mafi Golchin

Although genetic variants that affect susceptibility to coronary artery disease (CAD) have been greatly known, a number of these single nucleotide polymorphisms (SNPs) remain to be analyzed in populations with different ethnicities. CAD is influenced by numerous genetic, environmental, and lifestyle factors, and is an important reason for mortality around the globe. In this study, a novel SNP (...

Although genetic variants that affect susceptibility to coronary artery disease (CAD) have been greatly known, a number of these single nucleotide polymorphisms (SNPs) remain to be analyzed in populations with different ethnicities. CAD is influenced by numerous genetic, environmental, and lifestyle factors, and is an important reason for mortality around the globe. In this study, a novel SNP (...

2007
Michael Hölzel Thomas Grimm Michaela Rohrmoser Anastassia Malamoussi Thomas Harasim Anita Gruber-Eber Elisabeth Kremmer Dirk Eick

The nucleolar protein Pes1 interacts with Bop1 and WDR12 in a stable complex (PeBoW-complex) and its expression is tightly associated with cell proliferation. The yeast homologue Nop7p (Yph1p) functions in both, rRNA processing and cell cycle progression. The presence of a BRCT-domain (BRCA1 C-terminal) within Pes1 is quite unique for an rRNA processing factor, as this domain is normally found ...

Journal: :Revista espanola de cardiologia 2015
Michel Zabalza Isaac Subirana Carla Lluis-Ganella Sergi Sayols-Baixeras Eric de Groot Roman Arnold Ana Cenarro Rafel Ramos Jaume Marrugat Roberto Elosua

INTRODUCTION AND OBJECTIVES Recent studies have identified several genetic variants associated with coronary artery disease. Some of these genetic variants are not associated with classical cardiovascular risk factors and the mechanism of such associations is unclear. The aim of the study was to determine whether these genetic variants are related to subclinical atherosclerosis measured by caro...

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