نتایج جستجو برای: NEFL

تعداد نتایج: 100  

2012
Xiao-Qing Li Lin Li Chun-Hua Xiao Yu-Mei Feng

Neurofilament, light polypeptide (NEFL) was demonstrated to be ectopically expressed in breast cancer tissues and decreased in lymph node metastases compared to the paired primary breast cancers in our previous study. Moreover, in several studies, NEFL was regarded as a tumor suppressor gene, and its loss of heterozygosity (LOH) was related to carcinogenesis and metastasis in several types of c...

Journal: :Molecular cancer research : MCR 2012
Baishen Chen Ju Chen Michael G House Kevin J Cullen Kenneth P Nephew Zhongmin Guo

Resistance to cisplatin-based chemotherapy is responsible for therapeutic failure of many common human cancers including cancer of head and neck (HNC). Mechanisms underlying cisplatin resistance remain unclear. In this study, we identified neurofilament light polypeptide (NEFL) as a novel hypermethylated gene associated with resistance to cisplatin-based chemotherapy in HNC. Analysis of 14 HNC ...

Journal: :Archives of neurology 2007
Gabriel Miltenberger-Miltenyi Andreas R Janecke Julia V Wanschitz Vincent Timmerman Christian Windpassinger Michaela Auer-Grumbach Wolfgang N Löscher

BACKGROUND To date, 13 different neurofilament light-chain polypeptide gene (NEFL) mutations have been identified in 55 patients with Charcot-Marie-Tooth disease (CMT) from 16 families. NEFL mutations were found to be associated with axonal and demyelinating variants of CMT. OBJECTIVES To describe the clinical features of 11 patients with CMT and NEFL mutations and to explore possible genotyp...

2014
Mario Capasso Sharon Diskin Flora Cimmino Giovanni Acierno Francesca Totaro Giuseppe Petrosino Lucia Pezone Maura Diamond Lee McDaniel Hakon Hakonarson Achille Iolascon Marcella Devoto John M. Maris

The genetic etiology of sporadic neuroblastoma is still largely obscure. In a genome-wide association study, we identified single-nucleotide polymorphisms (SNP) associated with neuroblastoma at the CASC15, BARD1, LMO1, DUSP12, HSD17B12, HACE1, and LIN28B gene loci, but these explain only a small fraction of neuroblastoma heritability. Other neuroblastoma susceptibility genes are likely hidden a...

2015
Zeyou Wang Jing Yang Gang Xu Wei Wang Changhong Liu Honghui Yang Zhibin Yu Qianqian Lei Lan Xiao Jing Xiong Liang Zeng Juanjuan Xiang Jian Ma Guiyuan Li Minghua Wu

MicroRNA-381 (miR-381) is a highly expressed onco-miRNA that is involved in malignant progression and has been suggested to be a good target for glioblastoma multiforme (GBM) therapy. In this study, we employed two-dimensional fluorescence differential gel electrophoresis (2-D DIGE) and MALDI-TOF/TOF-MS/MS to identify 27 differentially expressed proteins, including the significantly upregulated...

2012
Baishen Chen Ju Chen Michael G. House Kevin J. Cullen Kenneth P. Nephew Zhongmin Guo

Resistance to cisplatin-based chemotherapy is responsible for therapeutic failure of many common human cancers including cancer of head and neck (HNC). Mechanisms underlying cisplatin resistance remain unclear. In this study, we identified neurofilament light polypeptide (NEFL) as a novel hypermethylated gene associated with resistance to cisplatin-based chemotherapy inHNC. Analysis of 14HNC ce...

Journal: :Human molecular genetics 2015
Adijat A Adebola Theo Di Castri Chui-Zhen He Laura A Salvatierra Jian Zhao Kristy Brown Chyuan-Sheng Lin Howard J Worman Ronald K H Liem

Charcot-Marie-Tooth disease (CMT) is the most commonly inherited neurological disorder with a prevalence of 1 in 2500 people worldwide. Patients suffer from degeneration of the peripheral nerves that control sensory information of the foot/leg and hand/arm. Multiple mutations in the neurofilament light polypeptide gene, NEFL, cause CMT2E. Previous studies in transfected cells showed that expres...

Journal: :Cancer research 2014
Mario Capasso Sharon Diskin Flora Cimmino Giovanni Acierno Francesca Totaro Giuseppe Petrosino Lucia Pezone Maura Diamond Lee McDaniel Hakon Hakonarson Achille Iolascon Marcella Devoto John M Maris

The genetic etiology of sporadic neuroblastoma is still largely obscure. In a genome-wide association study, we identified single-nucleotide polymorphisms (SNP) associated with neuroblastoma at the CASC15, BARD1, LMO1, DUSP12, HSD17B12, HACE1, and LIN28B gene loci, but these explain only a small fraction of neuroblastoma heritability. Other neuroblastoma susceptibility genes are likely hidden a...

2014
Muhammad Ishtiaq Danae Campos-Melo Kathryn Volkening Michael J. Strong

Amyotrophic lateral sclerosis (ALS) is a fatal disease characterized by progressive motor neuron degeneration and neurofilament aggregate formation. Spinal motor neurons in ALS also show a selective suppression in the levels of low molecular weight neurofilament (NEFL) mRNA. We have been interested in investigating the role of microRNAs (miRNAs) in NEFL transcript stability. MiRNAs are small, 2...

Journal: :JAMA neurology 2014
Pankaj B Agrawal Mugdha Joshi Nicholas S Marinakis Klaus Schmitz-Abe Pedro D S C Ciarlini Jane C Sargent Kyriacos Markianos Umberto De Girolami David A Chad Alan H Beggs

IMPORTANCE Newer sequencing technologies in combination with traditional gene mapping techniques, such as linkage analysis, can help identify the genetic basis of disease for patients with rare disorders of uncertain etiology. This approach may expand the phenotypic spectrum of disease associated with those genetic mutations. OBJECTIVE To elucidate the molecular cause of a neuromuscular disea...

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