نتایج جستجو برای: smarcal1

تعداد نتایج: 96  

Journal: :Circulation 2009
Seyedhossein Aharinejad Olena Andrukhova Matthias Gmeiner Anita Thomas Arezu Aliabadi Andreas Zuckermann Katharina Krenn Michael Grimm

BACKGROUND Primary graft dysfunction (PGD) is a life-threatening complication in cardiac transplantation. A sensitive, specific, and easily measurable predictor in donors could facilitate PGD prevention. METHODS AND RESULTS SMARCAL1 is a matrix-associated regulator of chromatin with helicase and ATPase activities, and its serum concentrations were significantly increased in a targeted protein...

Journal: :Human molecular genetics 2012
Alireza Baradaran-Heravi Kyoung Sang Cho Bas Tolhuis Mrinmoy Sanyal Olena Morozova Marie Morimoto Leah I Elizondo Darren Bridgewater Joanna Lubieniecka Kimberly Beirnes Clara Myung Danny Leung Hok Khim Fam Kunho Choi Yan Huang Kira Y Dionis Jonathan Zonana Kory Keller Peter Stenzel Christy Mayfield Thomas Lücke Arend Bokenkamp Marco A Marra Maarten van Lohuizen David B Lewis Chad Shaw Cornelius F Boerkoel

Biallelic mutations of the DNA annealing helicase SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like 1) cause Schimke immuno-osseous dysplasia (SIOD, MIM 242900), an incompletely penetrant autosomal recessive disorder. Using human, Drosophila and mouse models, we show that the proteins encoded by SMARCAL1 orthologs localize to transcriptionall...

Journal: :Genes & development 2013
Frank B Couch Carol E Bansbach Robert Driscoll Jessica W Luzwick Gloria G Glick Rémy Bétous Clinton M Carroll Sung Yun Jung Jun Qin Karlene A Cimprich David Cortez

The DNA damage response kinase ataxia telangiectasia and Rad3-related (ATR) coordinates much of the cellular response to replication stress. The exact mechanisms by which ATR regulates DNA synthesis in conditions of replication stress are largely unknown, but this activity is critical for the viability and proliferation of cancer cells, making ATR a potential therapeutic target. Here we use sel...

2016
Kelli E. Cox Alexandre Maréchal Rachel Litman Flynn

Cancer cells overcome replicative senescence by exploiting mechanisms of telomere elongation, a process often accomplished by reactivation of the enzyme telomerase. However, a subset of cancer cells lack telomerase activity and rely on the alternative lengthening of telomeres (ALT) pathway, a recombination-based mechanism of telomere elongation. Although the mechanisms regulating ALT are not fu...

2014
Frank B Couch David Cortez

Human cells must faithfully duplicate billions of base pairs of DNA every cell division cycle. Insufficient precursors, DNA damage, and difficult-to-replicate sequences cause replication fork stalling. Even in the best of circumstances, hundreds of forks may stall during each S phase in a human cell, and the frequency increases in cells exposed to genotoxic or oncogenic stresses. Cells must res...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Aaron C Mason Robert P Rambo Briana Greer Michael Pritchett John A Tainer David Cortez Brandt F Eichman

SMARCAL1, a DNA remodeling protein fundamental to genome integrity during replication, is the only gene associated with the developmental disorder Schimke immuno-osseous dysplasia (SIOD). SMARCAL1-deficient cells show collapsed replication forks, S-phase cell cycle arrest, increased chromosomal breaks, hypersensitivity to genotoxic agents, and chromosomal instability. The SMARCAL1 catalytic dom...

2012
Marie Morimoto Zhongxin Yu Peter Stenzel J Marietta Clewing Behzad Najafian Christy Mayfield Glenda Hendson Justin G Weinkauf Andrew K Gormley David M Parham Umakumaran Ponniah Jean-Luc André Yumi Asakura Mitra Basiratnia Radovan Bogdanović Arend Bokenkamp Dominique Bonneau Anna Buck Joel Charrow Pierre Cochat Isabel Cordeiro Georges Deschenes M Semin Fenkçi Pierre Frange Stefan Fründ Helen Fryssira Encarna Guillen-Navarro Kory Keller Salman Kirmani Christine Kobelka Petra Lamfers Elena Levtchenko David B Lewis Laura Massella D Ross McLeod David V Milford François Nobili Jorge M Saraiva C Nur Semerci Lawrence Shoemaker Nataša Stajić Anja Stein Doris Taha Dorothea Wand Jonathan Zonana Thomas Lücke Cornelius F Boerkoel

BACKGROUND Arteriosclerosis and emphysema develop in individuals with Schimke immuno-osseous dysplasia (SIOD), a multisystem disorder caused by biallelic mutations in SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like 1). However, the mechanism by which the vascular and pulmonary disease arises in SIOD remains unknown. METHODS We reviewed th...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010
Zhihui Yue Shiyi Xiong Liangzhong Sun Weijun Huang Ying Mo Liuyi Huang Xiaoyun Jiang Shumei Chen Bin Hu Yiming Wang

BACKGROUND Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive pleiotropic disease caused by mutations in the SMARCAL1 gene. To date there have been no data from the Chinese population. Here, we report the first SIOD case in the Chinese population. No case with gross carpal bone age retardation has been reported previously. METHODS The index patient was diagnosed by clinical...

2011
Mitra Basiratnia Alireza Baradaran-Heravi Majid Yavarian Bita Geramizadeh Mehran Karimi

Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphyseal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (SMARCAL1) gene are responsible for the disease. The present report describes, for the first time...

Journal: :The Turkish journal of pediatrics 2015
Ayşe İpek Polat Uluç Yiş Müge Ayanoğlu Ayşe Semra Hız Handan Güleryüz Tülay Öztürk Atasoy Cornelius F Boerkoel

Schimke immuno-osseous dysplasia is an autosomal recessive multisystem disorder caused by defects in SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like 1 gene (SMARCAL1). SMARCAL1 product is a helicase that has role in selective cellular proliferation. The disorder is characterized by spondyloepiphyseal dysplasia with short stature, nephropathy, T cell ...

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