نتایج جستجو برای: ncf2

تعداد نتایج: 100  

Journal: :Allergologia et immunopathologia 2016
T A Khan O Cabral-Marques L F Schimke E B de Oliveira E P Amaral M R D'Império Lima F Scancetti Tavares B T Costa Carvalho A Condino-Neto

Susceptibility to infections caused by Mycobacterium tuberculosis and other Mycobacterium species has been reported in patients with acquired immunodeficiencies (e.g., acquired immunodeficiency syndrome, or AIDS) or primary immunodeficiency diseases (PIDs), including defects of the IL-12/IFNaxis, severe combined immunodeficiency (SCID), CD40L deficiency, and chronic granulomatous disease (CGD)....

Journal: :The Journal of biological chemistry 1994
D J Uhlinger K L Taylor J D Lambeth

The neutrophil respiratory burst oxidase consists of both the plasma membrane-associated flavocytochrome b558 and cytosolic regulatory proteins including p47-phox, p67-phox, and a small GTP-binding protein (Rac1 and/or Rac2). Oxidase activation is thought to result from the assembly of the cytosolic components on the cytochrome. A model has been proposed in which p47-phox binds directly to the ...

Journal: :Insect biochemistry and molecular biology 1998
R Beckwitt S Arcidiacono R Stote

Spider silks are highly repetitive proteins, characterized by regions of polyalanine and glycine-rich repeating units. We have obtained two variants of the Spidroin 1 (NCF-1) silk gene sequence from Nephila clavipes. One sequence (1726 bp) was from a cloned cDNA, and the other (1951 bp) was from PCR of genomic DNA. When these sequences are compared with each other and the previously published S...

Journal: :Carcinogenesis 2009
Ji-Young Lee Ae Kyung Park Kyoung-Mu Lee Sue K Park Sohee Han Wonshik Han Dong-Young Noh Keun-Young Yoo Ho Kim Stephen J Chanock Nathaniel Rothman Daehee Kang

OBJECTIVES This study was conducted to investigate the role of common variation in innate immunity-related genes as susceptibility factors to breast cancer risk in Korean women. METHODS Total 1536 single-nucleotide polymorphisms (SNPs) in 203 genes were analyzed by Illumina GoldenGate assay in 209 cases and the same numbers of controls. Both SNP and gene-based tests were used to evaluate the ...

2017
Jing Wu Wei-Fan Wang Yi-Dan Zhang Tong-Xin Chen

Chronic Granulomatous Disease (CGD) is a rare inherited primary immunodeficiency, which is characterized by recurrent infections due to defective phagocyte NADPH oxidase enzyme. Nowadays, little is known about Chinese CGD patients. Here we report 48 CGD patients in our single center study, which is the largest cohort study from Mainland China. The ratio of male to female was 11 : 1. The mean on...

2014
Rabia T. Khan Kyoko E. Yuki Danielle Malo

Experimental animal models of Salmonella infections have been widely used to identify genes important in the host immune response to infection. Using an F2 cross between the classical inbred strain C57BL/6J and the wild derived strain MOLF/Ei, we have previously identified Ity3 (Immunity to Typhimurium locus 3) as a locus contributing to the early susceptibility of MOLF/Ei mice to infection wit...

2017
Pascal Trouvé Emmanuelle Génin Claude Férec

Cystic Fibrosis is the most common lethal autosomal recessive disorder in the white population, affecting among other organs, the lung, the pancreas and the liver. Whereas Cystic Fibrosis is a monogenic disease, many studies reveal a very complex relationship between genotype and clinical phenotype. Indeed, the broad phenotypic spectrum observed in Cystic Fibrosis is far from being explained by...

2015
Sharon O’Neill Julie Brault Marie-Jose Stasia Ulla G. Knaus

Maintaining the redox balance between generation and elimination of reactive oxygen species (ROS) is critical for health. Disturbances such as continuously elevated ROS levels will result in oxidative stress and development of disease, but likewise, insufficient ROS production will be detrimental to health. Reduced or even complete loss of ROS generation originates mainly from inactivating vari...

2016
Jiawei Xu Xiao Bao Zhaofeng Peng Linlin Wang Linqing Du Wenbin Niu Yingpu Sun

Polycystic ovary syndrome (PCOS) affects approximately 7% of the reproductive-age women. A growing body of evidence indicated that epigenetic mechanisms contributed to the development of PCOS. The role of DNA modification in human PCOS ovary granulosa cell is still unknown in PCOS progression. Global DNA methylation and hydroxymethylation were detected between PCOS' and controls' granulosa cell...

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