نتایج جستجو برای: mut t2

تعداد نتایج: 31546  

Journal: :Blood 2009
Bas J Wouters Bob Löwenberg Claudia A J Erpelinck-Verschueren Wim L J van Putten Peter J M Valk Ruud Delwel

Mutations in CCAAT/enhancer binding protein alpha (CEBPA) are seen in 5% to 14% of acute myeloid leukemia (AML) and have been associated with a favorable clinical outcome. Most AMLs with CEBPA mutations simultaneously carry 2 mutations (CEBPA(double-mut)), usually biallelic, whereas single heterozygous mutations (CEBPA(single-mut)) are less frequently seen. Using denaturing high-performance liq...

Journal: :Blood 2012
Frederik Damm Olivier Kosmider Véronique Gelsi-Boyer Aline Renneville Nadine Carbuccia Claire Hidalgo-Curtis Véronique Della Valle Lucile Couronné Laurianne Scourzic Virginie Chesnais Agnes Guerci-Bresler Bohrane Slama Odile Beyne-Rauzy Aline Schmidt-Tanguy Aspasia Stamatoullas-Bastard François Dreyfus Thomas Prébet Stéphane de Botton Norbert Vey Michael A Morgan Nicholas C P Cross Claude Preudhomme Daniel Birnbaum Olivier A Bernard Michaela Fontenay

A cohort of MDS patients was examined for mutations affecting 4 splice genes (SF3B1, SRSF2, ZRSR2, and U2AF35) and evaluated in the context of clinical and molecular markers. Splice gene mutations were detected in 95 of 221 patients. These mutations were mutually exclusive and less likely to occur in patients with complex cytogenetics or TP53 mutations. SF3B1(mut) patients presented with lower ...

Journal: :The Biochemical journal 2011
Brijesh Kumar Pandey Saurabh Srivastava Manish Singh Jimut Kanti Ghosh

Cytotoxicity, a major obstacle in therapeutic application of antimicrobial peptides, is controlled by leucine-zipper-like sequences in melittin and other naturally occurring antimicrobial peptides. Magainin 2 shows significantly lower cytotoxicity than many naturally occurring antimicrobial peptides and lacks this structural element. To investigate the consequences of introducing a leucine zipp...

2010
Rachel Sarig Noa Rivlin Ran Brosh Chamutal Bornstein Iris Kamer Osnat Ezra Alina Molchadsky Naomi Goldfinger Ori Brenner Varda Rotter

p53 deficiency enhances the efficiency of somatic cell reprogramming to a pluripotent state. As p53 is usually mutated in human tumors and many mutated forms of p53 gain novel activities, we studied the influence of mutant p53 (mut-p53) on somatic cell reprogramming. Our data indicate a novel gain of function (GOF) property for mut-p53, which markedly enhanced the efficiency of the reprogrammin...

2016
Peng-fei Wang Ning Liu Hong-wang Song Kun Yao Tao Jiang Shou-wei Li Chang-Xiang Yan

WHO2007 grading of diffuse gliomas in adults is well-established. However, IDH mutations make classification of gliomas according to the WHO2007 edition controversial. Here, we characterized IDH-1R132H mut status in a cohort of 670 adult patients with different WHO2007 grades of diffuse glioma. Patient characteristics, clinical data and prognoses were obtained from medical records. Patients wit...

Journal: :Nucleic Acids Research 2005
Bastiaan B. J. Tops Hiroaki Tabara Titia Sijen Femke Simmer Craig C. Mello Ronald H. A. Plasterk René F. Ketting

In Caenorhabditis elegans, the activity of transposable elements is repressed in the germline. One of the mechanisms involved in this repression is RNA interference (RNAi), a process in which dsRNA targets cleavage of mRNAs in a sequence-specific manner. The first gene found to be involved in RNAi and transposon silencing in C.elegans is mut-7, a gene encoding a putative exoribonuclease. Here, ...

2013
Federico Pozzo Michele Dal Bo Nadia Peragine Riccardo Bomben Antonella Zucchetto Francesca Maria Rossi Massimo Degan Davide Rossi Annalisa Chiarenza Alberto Grossi Francesco Di Raimondo Francesco Zaja Gabriele Pozzato Paola Secchiero Gianluca Gaidano Giovanni Del Poeta Giorgio Zauli Robin Foà Anna Guarini Valter Gattei

BACKGROUND TP53 defects, i.e., 17p13 deletion and/or nucleotide mutations, associate with short survival and chemorefractoriness in chronic lymphocytic leukemia (CLL). In this context, since direct sequencing of the TP53 gene does not evaluate TP53 functionality, a functional assessment of TP53 pathway may be of interest to identify high risk CLL. By taking advantage of a training cohort of 100...

2010
Jolan E. Walter Francesca Rucci Laura Patrizi Mike Recher Stephan Regenass Tiziana Paganini Marton Keszei Itai Pessach Philipp A. Lang Pietro Luigi Poliani Silvia Giliani Waleed Al-Herz Morton J. Cowan Jennifer M. Puck Jack Bleesing Tim Niehues Catharina Schuetz Harry Malech Suk See DeRavin Fabio Facchetti Andrew R. Gennery Emma Andersson Naynesh R. Kamani JoAnn Sekiguchi Hamid M. Alenezi Javier Chinen Ghassan Dbaibo Gehad ElGhazali Adriano Fontana Srdjan Pasic Cynthia Detre Cox Terhorst Frederick W. Alt Luigi D. Notarangelo

The contribution of B cells to the pathology of Omenn syndrome and leaky severe combined immunodeficiency (SCID) has not been previously investigated. We have studied a mut/mut mouse model of leaky SCID with a homozygous Rag1 S723C mutation that impairs, but does not abrogate, V(D)J recombination activity. In spite of a severe block at the pro-B cell stage and profound B cell lymphopenia, signi...

Journal: :Physiological genomics 2004
Ayumi Aurea Miyakawa Maria de Lourdes Junqueira José Eduardo Krieger

Mechanical forces contribute to maintenance of cardiovascular homeostasis via the control of release and production of vasoactive substances. We demonstrated previously that shear stress decreases rat ACE activity and expression. Using a reporter gene approach and mutagenesis, we show now that the classic shear stress responsive element or SSRE (GAGACC) contained within 1,274 bp of this promote...

2012
Ying Ni Xin He Jinlian Chen Jessica Moline Jessica Mester Mohammed S. Orloff Matthew D. Ringel Charis Eng

Cowden syndrome (CS), a Mendelian autosomal-dominant disorder, predisposes to breast, thyroid and other cancers. Germline mutations in phosphatase and tensin homolog (PTEN) have been recently reported in 23% of a large series of classic CS. Here, we validated our small (n = 10) pilot study in a large patient series that germline variations in succinate dehydrogenase genes (SDHx) occur in 8% (49...

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