نتایج جستجو برای: myh9 gene

تعداد نتایج: 1141526  

2015
Toshitsugu Fujita Fusako Kitaura Hodaka Fujii

Accumulating evidence suggests that Pax5 plays essential roles in B cell lineage commitment. However, molecular mechanisms of B cell-specific expression of Pax5 are not fully understood. Here, we applied insertional chromatin immunoprecipitation (iChIP) combined with stable isotope labeling using amino acids in cell culture (SILAC) (iChIP-SILAC) to direct identification of proteins interacting ...

Journal: :Haematologica 2002
Michele Di Pumpo Patrizia Noris Alessandro Pecci Anna Savoia Marco Seri Iride F Ceresa Carlo L Balduini

BACKGROUND AND OBJECTIVES May-Hegglin anomaly (MHA) and Sebastian syndrome (SBS) are inherited macrothrombocytopenias with D hle-like bodies in leukocytes. MHA-SBS are due to mutations of the gene (MYH9) for the heavy chain of non-muscle myosin IIA (NMMHC-IIA), the only myosin II expressed in platelets. The bleeding tendency is often more severe than expected on the basis of platelet count, but...

2010
George W. Nelson Barry I. Freedman Donald W. Bowden Carl D. Langefeld Ping An Pamela J. Hicks Meredith A. Bostrom Randall C. Johnson Jeffrey B. Kopp Cheryl A. Winkler

Admixture mapping recently identified MYH9 as a susceptibility gene for idiopathic focal segmental glomerulosclerosis (FSGS), HIV-associated nephropathy (HIVAN) and end-stage kidney disease attributed to hypertension (H-ESKD) in African Americans (AA). MYH9 encodes the heavy chain of non-muscle myosin IIA, a cellular motor involved in motility. A haplotype and its tagging SNPs spanning introns ...

2016
Yuka Yamashita Rei Matsuura Shinji Kunishima Yoshie Oikawa Hirotsugu Ariizumi Shoko Hamada Nahoko Shirato Ryu Matsuoka Kohichi Ogawa Akihiko Sekizawa

We diagnosed a primipara woman with an MYH9 disorder during her pregnancy. A peripheral blood smear with an immunofluorescence analysis is the established method of diagnosing MYH9 disorders. We provided genetic counseling, as required, which included apprising the woman of the inheritance pattern, the importance of a genetic analysis, and the potential delivery risks for the patient and her of...

Journal: :Blood 2006
Yujie Huang Hubing Shi Hao Zhou Xiaomin Song Shaopeng Yuan Yongzhang Luo

Nucleolin, originally described as a nuclear protein, was recently found to be expressed on the surface of endothelial cells during angiogenic. However, the functions of cell-surface nucleolin in angiogenic remain mysterious. Here we report that upon endothelial cells adhering to extracellular matrix components, vascular endothelial growth factor (VEGF) mobilizes nucleolin from nucleus to cell ...

2014
Alan R. Morrison Timur O. Yarovinsky Bryan D. Young Filipa Moraes Tyler D. Ross Nicolle Ceneri Jiasheng Zhang Zhen W. Zhuang Albert J. Sinusas Ruggero Pardi Martin A. Schwartz Michael Simons Jeffrey R. Bender

Myeloid cells are important contributors to arteriogenesis, but their key molecular triggers and cellular effectors are largely unknown. We report, in inflammatory monocytes, that the combination of chemokine receptor (CCR2) and adhesion receptor (β2 integrin) engagement leads to an interaction between activated Rac2 and Myosin 9 (Myh9), the heavy chain of Myosin IIA, resulting in augmented vas...

Journal: :Platelets 2016
Eva Zetterberg Margareta S Carlsson Alle Juliane Najm Andreas Greinacher

MYH9-related platelet disorders are inherited macrothrombocytopenias with additional clinical manifestations including renal failure, hearing loss, pre-senile cataract, and inclusion bodies in leucocytes that are present in different combinations. The MYH9 gene codes for the cytoplasmic contractile protein non-muscular myosin heavy chain IIA, present in several tissues. The bleeding tendency is...

Journal: :Gastrointestinal endoscopy 2015
Vinay Chandrasekhara Krishnavel V Chathadi Ruben D Acosta G Anton Decker Dayna S Early Mohamad A Eloubeidi John A Evans Ashley L Faulx Robert D Fanelli Deborah A Fisher Kimberly Foley Lisa Fonkalsrud Joo Ha Hwang Terry L Jue Mouen A Khashab Jenifer R Lightdale V Raman Muthusamy Shabana F Pasha John R Saltzman Ravi Sharaf Aasma Shaukat Amandeep K Shergill Amy Wang Brooks D Cash John M DeWitt

Vinay Chandrasekhara, MD, Krishnavel V. Chathadi, MD, Ruben D. Acosta, MD, G. Anton Decker, MBBCh, MRCP, MHA, Dayna S. Early, MD, Mohamad A. Eloubeidi, MD, John A. Evans, MD, Ashley L. Faulx, MD, Robert D. Fanelli, MD, SAGES Representative, Deborah A. Fisher, MD, MHS, Kimberly Foley, RN, BSN, CGRN, SGNA Representative, Lisa Fonkalsrud, BSN, RN, SGNA Representative, Joo Ha Hwang, MD, PhD, Terry ...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2009
Barry I Freedman Pamela J Hicks Meredith A Bostrom Mary E Comeau Jasmin Divers Anthony J Bleyer Jeffrey B Kopp Cheryl A Winkler George W Nelson Carl D Langefeld Donald W Bowden

BACKGROUND Although MYH9 is strongly associated with biopsy-proven idiopathic and HIV-associated focal segmental glomerulosclerosis (FSGS) and clinically diagnosed 'hypertension-associated' end-stage renal disease (ESRD) in African Americans, its role in type 2 diabetes mellitus (T2DM)-associated ESRD is unclear. METHODS To assess whether MYH9 was associated with T2DM-ESRD, 751 African Americ...

Journal: :JPEN. Journal of parenteral and enteral nutrition 2016
David A August

Adequate Nutrition May get You Home: Effect of Caloric/Protein Deficits on the Discharge Destination of Critically Ill Surgical Patients 37 D. Dante Yeh, MD; Eva Fuentes, MD; Sadeq A. Quraishi, MD, MHA, MMScH; Catrina Cropano, MSc; Haytham Kaafarani, MD, MPH; Jarone Lee, MD, MPH; David R. King, MD; Marc DeMoya, MD; Peter Fagenholz, MD; Kathryn Butler, MD; Yuchiao Chang, PhD; and George Velmahos...

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