Results 71 to 80 of about 38,073 (235)

Insights into Novel Infant Milk Formula Bioactives

open access: yesNutrition and Dietary Supplements, 2020
Jordan Skolnick,1 Claire Chou,1 John Miklavcic1,2 1Schmid College of Science and Technology, Chapman University, Orange, CA 92866, USA; 2School of Pharmacy, Chapman University, Irvine, CA 92618, USACorrespondence: John MiklavcicSchmid College of Science ...
Skolnick J, Chou C, Miklavcic J
doaj  

Anti-GD2/4-1BB chimeric antigen receptor T cell therapy for the treatment of Chinese melanoma patients

open access: yesJournal of Hematology & Oncology, 2018
Background Chimeric antigen receptor (CAR)-engineered T cells have demonstrated promising clinical efficacy in patients with B cell lymphoma. However, the application of CAR-T cell therapy in the treatment of other solid tumors has been limited.
Jiayi Yu   +13 more
doaj   +1 more source

Sphingolipids: membrane microdomains in brain development, function and neurological diseases [PDF]

open access: yesOpen Biology, 2017
Sphingolipids are highly enriched in the nervous system where they are pivotal constituents of the plasma membranes and are important for proper brain development and functions. Sphingolipids are not merely structural elements, but are also recognized as
Anne S. B. Olsen, Nils J. Færgeman
doaj   +1 more source

Weitere Ganglioside aus Menschenhirn

open access: yes, 1964
Aus Menschenhirn konnten vier noch unbekannte Ganglioside, die nur in geringer Menge vorkommen, chromatographisch abgetrennt und näher charakterisiert werden: GGal (mit 1 Galaktose + 1 Lactaminsäure), GLact (mit 1 Lactose + 1 Lactaminsäure), G′Lact (mit ...
Wiegandt, H., Kuhn, R.
core   +1 more source

Guillain‐Barré Syndrome in Late Pregnancy Following Respiratory Syncytial Virus Infection: A Diagnostic Dilemma

open access: yesClinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT The diagnosis of Guillain–Barré syndrome (GBS) relies on evolving clinical features, supported by cerebrospinal fluid (CSF), laboratory investigations, and electrodiagnostic studies. Early investigations may be nondiagnostic and should not delay treatment when progressive neurological deterioration raises clinical suspicion of GBS.
Rhiana Pereira‐Lindley   +2 more
wiley   +1 more source

The effect of ganglioside on diabetic neurogenic bladder [PDF]

open access: yes, 1990
The effect of ganglioside was studied in 6 diabetic patients with neurogenic bladder. Ganglioside is glycosphingolipids which seems to be involved in the processes of nerve growth, regeneration and tissue reinnervation.
安本, 亮二   +2 more
core  

Characterization of GM1 ganglioside by direct inlet chemical ionization mass spectrometry.

open access: yesJournal of Lipid Research, 1982
Intact permethylated and permethylated-reduced (LiAlH4) derivatives of GM1 ganglioside were analyzed by direct inlet ammonia chemical ionization (CI) mass spectrometry. In addition, the trimethylsilylated derivative of the permethylated-reduced sample of
T Ariga   +4 more
doaj   +1 more source

Structural dynamics and pH‐regulated membrane binding of the TRAF2‐NC trimer

open access: yesProtein Science, Volume 35, Issue 11, November 2026.
Abstract Tumor necrosis factor receptor‐associated factor 2 (TRAF2) is a key adaptor in TNF receptor‐signaling that operates as a trimeric assembly. Here we investigate the structural and functional properties of a TRAF2 construct spanning the trimerization and receptor‐binding domains (TRAF2‐NC, residues 266–501).
Federica Cossu   +9 more
wiley   +1 more source

Establishment of various ganglioside-expressing cells.

open access: yes, 2018
(A) Biosynthetic pathway of gangliosides and glycolsyltransferase cDNAs used to establish various ganglioside-expressing cells. (B) Flow cytometry of ganglioside expression on GM2-, GM1-, GD3-, and GD2-expressing transfectans.
Orie Tajima (48929)   +7 more
core   +1 more source

Atypical juvenile presentation of GM2 gangliosidosis AB in a patient compound-heterozygote for c.259G>T and c.164C>T mutations in the GM2A gene

open access: yesMolecular Genetics and Metabolism Reports, 2017
GM2-gangliosidosis, AB variant is an extremely rare autosomal recessive inherited disorder caused by mutations in the GM2A gene that encodes GM2 ganglioside activator protein (GM2AP).
Carla Martins   +6 more
doaj   +1 more source

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