نتایج جستجو برای: 19±1?c

تعداد نتایج: 17  

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011
Bruno Marques Costa Marta Viana-Pereira Ricardo Fernandes Sandra Costa Paulo Linhares Rui Vaz Céline Pinheiro Jorge Lima Paula Soares Ana Silva Fernando Pardal Júlia Amorim Rui Nabiço Rui Almeida Carlos Alegria Manuel Melo Pires Célia Pinheiro Ernesto Carvalho Pedro Oliveira José M Lopes Rui M Reis

BACKGROUND The epidermal growth factor receptor (EGFR) regulates important cellular processes and is frequently implicated in human tumors. Three EGFR polymorphisms have been described as having a transcriptional regulatory function: two single-nucleotide polymorphisms in the essential promoter region, -216G/T and -191C/A, and a polymorphic (CA)(n) microsatellite sequence in intron 1. We aimed ...

Journal: :Cancer research 2005
Wanqing Liu Federico Innocenti Michael H Wu Apurva A Desai M Eileen Dolan Edwin H Cook Mark J Ratain

The epidermal growth factor receptor (EGFR) plays a prominent role in cell growth and development. Its regulation in humans is complex and incompletely understood. In this study, 12 new polymorphisms were discovered in the 5'-regulatory region of EGFR gene and 2 common single nucleotide polymorphisms (-216G/T and -191C/A) were found in the essential promoter area, one of which is located in a S...

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2011
Yi-Fen Lo Kandai Nozu Kazumoto Iijima Takahiro Morishita Che-Chung Huang Sung-Sen Yang Huey-Kang Sytwu Yu-Wei Fang Min-Hua Tseng Shih-Hua Lin

BACKGROUND AND OBJECTIVES Gitelman's syndrome (GS) is an autosomal recessive renal tubular disorder caused by mutations in the SLC12A3 gene encoding the thiazide-sensitive Na(+)-Cl(-) cotransporter (NCC). Despite meticulous sequencing of genomic DNA, approximately one-third of GS patients are negative or heterozygotes for the known mutations. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS Beca...

2012
MASAYUKI SHITARA HIDEFUMI SASAKI KEISUKE YOKOTA KATSUHIRO OKUDA YU HIKOSAKA SATORU MORIYAMA MOTOKI YANO TOMOYA KAWAGUCHI AKIHITO KUBO MINORU TAKADA NAOTO KITAHARA MEINOSHIN OKUMURA AKIHIDE MATSUMURA KEIJI IUCHI YOSHITAKA FUJII

The epidermal growth factor receptor (EGFR) gene is highly polymorphic and its expression and activity may be affected by various polymorphisms. There have been several studies examining associations between EGFR polymorphisms and clinical outcome of lung cancer therapy; however, the underlying mechanism is largely unknown. The present study investigated EGFR polymorphism status and its correla...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2008
G Milano M-C Etienne-Grimaldi L Dahan M Francoual J-P Spano D Benchimol M Chazal C Letoublon T André F-N Gilly J-R Delpero J-L Formento

BACKGROUND In advanced colorectal cancer, K-Ras somatic mutations predict resistance to mAbs targeting epidermal growth factor receptor (EGFR). Relationships between K-Ras mutations and EGFR status have not been examined so far. We analyzed relationships between K-Ras mutations and EGFR tumoral status based on EGFR germinal polymorphisms, gene copy number and expression. METHODS Eighty colore...

Journal: :Anticancer research 2013
Yuko Kamata Akiko Kuhara Takeo Iwamoto Kazumi Hayashi Shigeo Koido Takahiro Kimura Shin Egawa Sadamu Homma

BACKGROUND/AIM Since antigenic peptides of the cancer-associated antigens presented on human leukocyte antigen (HLA) molecules are recognized by specific cytotoxic T-lymphocytes, they have the potential to becoming effective peptide vaccines for cancer immunotherapy. MATERIALS AND METHODS Peptides binding to HLA-A*0201 and HLA-A*2402 obtained from human prostate cancer cells by acid-elution w...

2014
Livia Garavelli Lucia Santoro Alexandra Iori Giancarlo Gargano Silvia Braibanti Simona Pedori Nives Melli Daniele Frattini Lucia Zampini Tiziana Galeazzi Lucia Padella Stefano Pepe Anita Wischmeijer Simonetta Rosato Ivan Ivanovski Lorenzo Iughetti Chiara Gelmini Sergio Bernasconi Andrea Superti-Furga Andrea Ballabio Orazio Gabrielli

Multiple Sulfatase Deficiency (MSD; OMIM 272200) is a rare autosomal recessive inborn error of metabolism caused by mutations in the sulfatase modifying factor 1 gene, encoding the formylglycine-generating enzyme (FGE), and resulting in tissue accumulation of sulfatides, sulphated glycosaminoglycans, sphingolipids and steroid sulfates. Less than 50 cases have been published so far. We report a ...

Journal: :Molecular cancer therapeutics 2010
Elisa Giovannetti Paolo A Zucali Godefridus J Peters Filippo Cortesi Armida D'Incecco Egbert F Smit Alfredo Falcone Jacobus A Burgers Armando Santoro Romano Danesi Giuseppe Giaccone Carmelo Tibaldi

EGFR mutations are strongly predictive of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor activity in non-small cell lung cancer (NSCLC), but resistance mechanisms are not completely understood. The interindividual variability in toxicity also points out to the need of novel pharmacogenetic markers to select patients before therapy. Therefore, we evaluated the associations bet...

Journal: :The Journal of infectious diseases 2002
Alison M Vine Aviva D Witkover Alun L Lloyd Katie J M Jeffery Asna Siddiqui Sara E F Marshall Mike Bunce Nobutaka Eiraku Shuji Izumo Koichiro Usuku Mitsuhiro Osame Charles R M Bangham

Human T lymphotropic virus type I (HTLV-I)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is one outcome of infection with HTLV-I. A population association study of 229 patients with HAM/TSP and 202 healthy carriers of HTLV-I in southern Japan showed that this outcome of HTLV-I infection and the HTLV-I provirus load are under polygenic control. Of 58 polymorphic sites studied in 3...

Journal: :Human mutation 2015
Ginevra Zanni Vera M Kalscheuer Andreas Friedrich Sabina Barresi Paolo Alfieri Matteo Di Capua Stefan A Haas Giorgia Piccini Thomas Karl Sabine M Klauck Emanuele Bellacchio Francesco Emma Marco Cappa Enrico Bertini Lore Breitenbach-Koller

RPL10 encodes ribosomal protein L10 (uL16), a highly conserved multifunctional component of the large ribosomal subunit, involved in ribosome biogenesis and function. Using X-exome resequencing, we identified a novel missense mutation (c.191C>T; p.(A64V)) in the N-terminal domain of the protein, in a family with two affected cousins presenting with X-linked intellectual disability, cerebellar h...

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