نتایج جستجو برای: 3805 gm2

تعداد نتایج: 775  

2013
Yasuhiro Ogawa Makoto Tanaka Miho Tanabe Toshihiro Suzuki Tadayasu Togawa Tomoko Fukushige Takuro Kanekura Hitoshi Sakuraba Kazuhiko Oishi

Sandhoff disease (SD) is a glycosphingolipid storage disease that arises from mutations in the Hexb gene and the resultant deficiency in β-hexosaminidase activity. This deficiency results in aberrant lysosomal accumulation of the ganglioside GM2 and related glycolipids, and progressive deterioration of the central nervous system. Dysfunctional glycolipid storage causes severe neurodegeneration ...

Journal: :The American journal of tropical medicine and hygiene 1999
A H Gori K Ahmed G Martinez H Masaki K Watanabe T Nagatake

Melioidosis is the term given to any infection caused by Burkholderia pseudomallei. This bacteria is one of the important causative agents of life-threatening pulmonary infections in the tropical and subtropical areas. The initiation of respiratory infections is attachment of this bacteria to pharyngeal cells. The precise mechanism of attachment of B. pseudomallei is not known. In this study, w...

Journal: :Human molecular genetics 2011
Timothy J Sargeant Susan Wang Josephine Bradley Nicolas J C Smith Animesh A Raha Rosamund McNair Robin J Ziegler Seng H Cheng Timothy M Cox Maria Begoña Cachón-González

Sandhoff disease, a GM2 gangliosidosis caused by a deficiency in β-hexosaminidase, is characterized by progressive neurodegeneration. Although loss of neurons in association with lysosomal storage of glycosphingolipids occurs in patients with this disease, the molecular pathways that lead to the accompanying neurological defects are unclear. Using an authentic murine model of GM2 gangliosidosis...

Journal: :Journal of lipid research 2013
Martin Fan Rohini Sidhu Hideji Fujiwara Brett Tortelli Jessie Zhang Cristin Davidson Steven U Walkley Jessica H Bagel Charles Vite Nicole M Yanjanin Forbes D Porter Jean E Schaffer Daniel S Ory

Niemann-Pick type C (NPC)1 is a rare neurodegenerative disease for which treatment options are limited. A major barrier to development of effective treatments has been the lack of validated biomarkers to monitor disease progression or serve as outcome measures in clinical trials. Using targeted metabolomics to exploit the complex lipid storage phenotype that is the hallmark of NPC1 disease, we ...

Journal: :The Journal of Experimental Medicine 2003
Dianna Y. Wu Neil H. Segal Stephane Sidobre Mitchell Kronenberg Paul B. Chapman

GD3, a ganglioside expressed on human melanoma, can be recognized by the humoral immune system. In this paper, we demonstrate that immunizing mice with the human melanoma cell line SK-MEL-28 (GD3+ GM2- CD1-) or with syngeneic APCs loaded with GD3 can induce a GD3-reactive natural killer T (NKT) cell response. GD3-reactive NKT cells were detected among splenocytes of immunized mice at frequencie...

2012
H Aryan O Aryani K Banihashemi T Zaman M Houshmand

BACKGROUND Sandhoff disease is an autosomal recessive disorder caused by β-hexosaminidase deficiency and accumulation of GM2 ganglioside resulting in progressive motor neuron manifestations and death from respiratory failure and infections in infantiles. Pathogenic mutations in HEXB gene were observed which leads to enzyme activity reduction and interruption of normal metabolic cycle of GM2 gan...

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