نتایج جستجو برای: gm1

تعداد نتایج: 1944  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Nobuhiro Yuki Keiichiro Susuki Michiaki Koga Yukihiro Nishimoto Masaaki Odaka Koichi Hirata Kyoji Taguchi Tadashi Miyatake Koichi Furukawa Tetsuji Kobata Mitsunori Yamada

Molecular mimicry between microbial and self-components is postulated as the mechanism that accounts for the antigen and tissue specificity of immune responses in postinfectious autoimmune diseases. Little direct evidence exists, and research in this area has focused principally on T cell-mediated, antipeptide responses, rather than on humoral responses to carbohydrate structures. Guillain-Barr...

Journal: :Molecular biology of the cell 2004
Bridget S Wilson Stanly L Steinberg Karin Liederman Janet R Pfeiffer Zurab Surviladze Jun Zhang Lawrence E Samelson Li-Hong Yang Paul G Kotula Janet M Oliver

Lipid rafts isolated by detergent extraction and sucrose gradient fractionation from mast cells are enriched for the glycosylphosphatidylinositol-linked protein Thy-1, the ganglioside GM1, palmitoylated LAT, and cross-linked IgE receptors, FcepsilonRI. This study addresses the relationship of fractionation data to the organization of raft markers in native membranes. Immunogold labeling and ele...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Thomas S van Zanten Jordi Gómez Carlo Manzo Alessandra Cambi Javier Buceta Ramon Reigada Maria F Garcia-Parajo

Lateral segregation of cell membranes is accepted as a primary mechanism for cells to regulate a diversity of cellular functions. In this context, lipid rafts have been conceptualized as organizing principle of biological membranes where underlying cholesterol-mediated selective connectivity must exist even at the resting state. However, such a level of nanoscale compositional connectivity has ...

Journal: :AJNR. American journal of neuroradiology 2009
E De Grandis M Di Rocco A Pessagno E Veneselli A Rossi

SUMMARY Late infantile GM1 gangliosidosis is a rare lysosomal disorder characterized by mental deterioration and progressive spastic, cerebellar, and extrapyramidal signs, without facial dysmorphisms and organomegaly. Neuroimaging findings have been reported in only a few cases. Here we report on predominant globus pallidus MR signal-intensity abnormalities in 2 patients with the late infantile...

Journal: :Cell structure and function 1986
H Asou N Mutou S Hirano T Takagi K Kajiwara J Komatsubara E Sugaya

Localization of ganglioside GM1 in cholinergic neurons from the septal area of a primary culture newborn rat brain was studied with a double avidin-biotin complex system. Cholinergic neurons were identified by double immunolabeling techniques that use choline acetyltransferase (ChAT) and neurofilament (NF) protein-antibodies. ChAT-positive neurons also were stained for ganglioside GM1 by using ...

2016
Marco Diociaiuti Cristiano Giordani Gihan S. Kamel Francesco Brasili Simona Sennato Cecilia Bombelli Karen Y. Meneses Marco A. Giraldo Federico Bordi

GM1 ganglioside is known to be involved in the amyloid-associated diseases and it is a crucial factor for the assembly of amyloid proteins on lipid-rafts, which are lipid structures located on the synaptic plasma membranes. Due to its slow aggregation rate, we employed salmon calcitonin (sCT) as a suitable probe representative of amyloid proteins, to study the interaction between this class of ...

2008
Tanya Das Gaurisankar Sa Cynthia Hilston Daisuke Kudo Patricia Rayman Kaushik Biswas Luis Molto Ronald Bukowski Brian Rini James H. Finke Charles Tannenbaum

The ability to induce T-cell apoptosis is one mechanism by which tumors evade the immune system, although the molecules involved remain controversial. We found that renal cell carcinoma (RCC)–induced T-cell apoptosis was inhibited by >50% when cocultures were performed with gangliosidedepleted tumor cells, caspase-8–negative lymphocytes, or anti–tumor necrosis factor-A (TNFA) antibodies, sugges...

2018
Maxmore Chaibva Xiang Gao Pranav Jain Warren A. Campbell Shelli L. Frey Justin Legleiter

Huntington disease (HD) is an inherited neurodegenerative disease caused by the expansion beyond a critical threshold of a polyglutamine (polyQ) tract near the N-terminus of the huntingtin (htt) protein. Expanded polyQ promotes the formation of a variety of oligomeric and fibrillar aggregates of htt that accumulate into the hallmark proteinaceous inclusion bodies associated with HD. htt is also...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Lee M Krug Govind Ragupathi Chandra Hood Mark G Kris Vincent A Miller Jennifer R Allen Stacy J Keding Samuel J Danishefsky Jorge Gomez Leslie Tyson Barbara Pizzo Valerie Baez Philip O Livingston

PURPOSE Immunotherapy directed toward cell surface antigens may provide a novel approach to the eradication of chemoresistant micrometastatic disease in patients with small-cell lung cancer (SCLC). Studies in SCLC cell lines and human tissues suggest that the ganglioside fucosyl GM1 is an abundant yet specific target. A prior clinical study demonstrated the potent immunogenicity of fucosyl GM-1...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1999
M N Dickler G Ragupathi N X Liu C Musselli D J Martino V A Miller M G Kris F T Brezicka P O Livingston S C Grant

Although small cell lung cancer (SCLC) is highly responsive to chemotherapy, relapses are common, and most patients die within 2 years of diagnosis. After initial therapy, standard treatment is observation alone. We have been investigating immunization against selected gangliosides as adjuvant therapy directed against residual and presumably resistant disease persisting after chemotherapy and i...

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