نتایج جستجو برای: cd6

تعداد نتایج: 223  

2012
Sophine B. Krintel Laurent Essioux Assaf Wool Julia S. Johansen Ehud Schreiber Tomer Zekharya Pinchas Akiva Mikkel Østergaard Merete L. Hetland

BACKGROUND TNFα inhibitor therapy has greatly improved the treatment of patients with rheumatoid arthritis, however at least 30% do not respond. We aimed to investigate insertions and deletions (INDELS) associated with response to TNFα inhibitors in patients with rheumatoid arthritis (RA). METHODOLOGY AND PRINCIPAL FINDINGS In the DANBIO Registry we identified 237 TNFα inhibitor naïve patient...

2013
Ellen M. Mowry Robert F. Carey Maria R. Blasco Jean Pelletier Pierre Duquette Pablo Villoslada Irina Malikova Elaine Roger R. Phillip Kinkel Jamie McDonald Peter Bacchetti Emmanuelle Waubant

OBJECTIVE Patients with early multiple sclerosis (MS) have stereotyped attack severity and recovery. We sought to determine if polymorphisms in MS susceptibility genes are associated with these attack features or with the risk of a second attack. METHODS 503 white subjects evaluated within a year of MS onset were included in the study. The severity of and recovery from the first two attacks w...

2015
Tara K. Sigdel Oriol Bestard Tim Q. Tran Szu-Chuan Hsieh Silke Roedder Izabella Damm Flavio Vincenti Minnie M. Sarwal Niels Olsen Saraiva Câmara

BACKGROUND Whole genome microarray meta-analyses of 1030 kidney, heart, lung and liver allograft biopsies identified a common immune response module (CRM) of 11 genes that define acute rejection (AR) across different engrafted tissues. We evaluated if the CRM genes can provide a molecular microscope to quantify graft injury in acute rejection (AR) and predict risk of progressive interstitial fi...

Journal: :Clinical chemistry 2003
Christina Vrettou Joanne Traeger-Synodinos Maria Tzetis George Malamis Emmanuel Kanavakis

BACKGROUND Hemoglobinopathies are priority genetic diseases for prevention programs. Rapid genotype characterization is fundamental in the diagnostic laboratory, especially when offering prenatal diagnosis for carrier couples. METHODS As a model, we designed a protocol based on the LightCycler technology to screen for a spectrum of beta-globin gene mutations in the Greek population. Design wa...

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