نتایج جستجو برای: idh

تعداد نتایج: 2014  

Journal: :Blood 2015
Zachary J Reitman Sergey A Sinenko Eric P Spana Hai Yan

Gain-of-function mutations in nicotinamide adenine dinucleotide phosphate-dependent isocitrate dehydrogenase (IDH)1 and IDH2 frequently arise in human leukemias and other cancers and produce high levels of D-2-hydroxyglutarate (D-2HG). We expressed the R195H mutant of Drosophila Idh (CG7176), which is equivalent to the human cancer-associated IDH1-R132H mutant, in fly tissues using the UAS-Gal4...

Journal: :Neuro-oncology 2013
Terri Rice Shichun Zheng Paul A Decker Kyle M Walsh Paige Bracci Yuanyuan Xiao Lucie S McCoy Ivan Smirnov Joseph S Patoka Helen M Hansen George Hsuang Joe L Wiemels Tarik Tihan Alexander R Pico Michael D Prados Susan M Chang Mitchel S Berger Alissa Caron Stephanie Fink Thomas Kollmeyer Amanda Rynearson Jesse Voss Matthew L Kosel Brooke L Fridley Daniel H Lachance Jeanette E Eckel-Passow Hugues Sicotte Brian Patrick O'Neill Caterina Giannini John K Wiencke Robert B Jenkins Margaret R Wrensch

INTRODUCTION Recent discoveries of inherited glioma risk loci and acquired IDH mutations are providing new insights into glioma etiology. IDH mutations are common in lower grade gliomas and secondary glioblastomas and uncommon in primary glioblastomas. Because the inherited variant in 11q23 has been associated with risk of lower grade glioma and not with glioblastomas, we hypothesized that this...

2016
Marijana Virijevic Teodora Karan-Djurasevic Irena Marjanovic Natasa Tosic Mirjana Mitrovic Irena Djunic Natasa Colovic Ana Vidovic Nada Suvajdzic-Vukovic Dragica Tomin Sonja Pavlovic

BACKGROUND Mutations in the isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) genes are frequent molecular lesions in acute myeloid leukaemia with normal karyotype (AML-NK). The effects of IDH mutations on clinical features and treatment outcome in AML-NK have been widely investigated, but only a few studies monitored these mutations during follow-up. PATIENTS AND METHODS In our study samples ...

2017
Lin Eric Huang Adam L. Cohen Howard Colman Randy L. Jensen Daniel W. Fults William T. Couldwell

Mutations of the isocitrate dehydrogenase (IDH) 1 and 2 genes occur in ~80% of lower-grade (WHO grade II and grade III) gliomas. Mutant IDH produces (R)-2-hydroxyglutarate, which induces DNA hypermethylation and presumably drives tumorigenesis. Interestingly, IDH mutations are associated with improved survival in glioma patients, but the underlying mechanism for the difference in survival remai...

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2008
Mira Rho Mark A Perazella Chirag R Parikh Aldo J Peixoto Ursula C Brewster

BACKGROUND AND OBJECTIVES Arginine vasopressin (AVP), an endogenous hormone with vasopressor properties, may be inadequately secreted during episodes of intradialytic hypotension (IDH). DESIGN, SETTING, PARTICIPANTS, AND MEASUREMENTS To evaluate this, we performed a prospective, observational pilot study of 20 chronic hemodialysis patients assessing the baseline AVP level and trend of AVP wit...

2015
Ki Yong Na Byeong-Joo Noh Ji-Youn Sung Youn Wha Kim Eduardo Santini Araujo Yong-Koo Park

BACKGROUND Isocitrate dehydrogenase (IDH) catalyzes the oxidative decarboxylation of isocitrate to yield α-ketoglutarate (α-KG) with production of reduced nicotinamide adenine dinucleotide (NADH). Dysfunctional IDH leads to reduced production of α-KG and NADH and increased production of 2-hydroxyglutarate, an oncometabolite. This results in increased oxidative damage and stabilization of hypoxi...

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...

2014
Xiao-Wei Wang Pietro Ciccarino Marta Rossetto Blandine Boisselier Yannick Marie Virginie Desestret Vincent Gleize Karima Mokhtari Marc Sanson Marianne Labussière

IDH1/2 mutation is the most frequent genomic alteration found in gliomas, affecting 40% of these tumors and is one of the earliest alterations occurring in gliomagenesis. We investigated a series of 1305 gliomas and showed that IDH mutation is almost constant in 1p19q codeleted tumors. We found that the distribution of IDH1(R132H) , IDH1(nonR132H) , and IDH2 mutations differed between astrocyti...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2014
Firoz Ahmad Rupali Mohota Savita Sanap Swarna Mandava Bibhu Ranjan Das

Mutations in the DNMT3A and IDH genes represent the most common genetic alteration after FLT3/NPM1 in acute myeloid leukemia (AML). We here analyzed the frequency and distribution pattern of DNMT3A and IDH mutations and their associations with other molecular markers in normal karyotype AML patients. Forty- five patients were screened for mutations in DNMT3A (R882), IDH1 (R132) and IDH2 (R140 a...

Journal: :Journal of bacteriology 1994
M I Muro-Pastor F J Florencio

NADP(+)-isocitrate dehydrogenase (NADP(+)-IDH) from the dinitrogen-fixing filamentous cyanobacterium Anabaena sp. strain PCC 7120 was purified to homogeneity. The native enzyme is composed of two identical subunits (M(r), 57,000) and cross-reacts with antibodies obtained against the previously purified NADP(+)-IDH from the unicellular cyanobacterium Synechocystis sp. strain PCC 6803. Anabaena N...

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