Results 41 to 50 of about 45,384 (211)

Differential expression of gut protein genes and population density of Arsenophonus contributes to sex-biased transmission of Bemisia tabaci vectored Cotton leaf curl virus.

open access: yesPLoS ONE, 2021
Whitefly, Bemisia tabaci (Gennadius) is an important pest of cotton causing direct damage as sap feeder and vector of Cotton leaf curl virus (CLCuV). Previous few studies suggest that female whiteflies are more efficient vector of begomovirusthan males ...
Ikbalpreet Singh   +4 more
doaj   +1 more source

Cyclophilin-A is bound to through its peptidylprolyl isomerase domain to the cytoplasmic dynein motor protein complex [PDF]

open access: yes, 2004
Although cyclophilin A (CyP-A) is a relatively abundant small immunophilin present in the cytoplasm of all mammalian cells, its general function(s) in the absence of the immunosuppressant drug cyclosporin A is not known.
Galigniana, Mario Daniel   +3 more
core   +2 more sources

Human cyclophilin B: a second cyclophilin gene encodes a peptidyl-prolyl isomerase with a signal sequence. [PDF]

open access: yesProceedings of the National Academy of Sciences, 1991
We report the cloning and characterization of a cDNA encoding a second human cyclosporin A-binding protein (hCyPB). Homology analyses reveal that hCyPB is a member of the cyclophilin B (CyPB) family, which includes yeast CyPB, Drosophila nina A, and rat cyclophilin-like protein.
E R, Price   +5 more
openaire   +2 more sources

Identification of a non-mammalian leptin-like gene:characterization and expression in the tiger salamander (Ambystoma tigrinum) [PDF]

open access: yes, 2006
Leptin is well established as a multifunctional cytokine in mammals. However, little is known about the evolution of the leptin gene in other vertebrates. A recently published set of ESTs from the tiger salamander (Ambystoma tigrinum) contains a sequence
Boswell, Timothy   +5 more
core   +1 more source

Receptor‐Mediated Transcytosis of Cyclophilin B Through the Blood—Brain Barrier [PDF]

open access: yesJournal of Neurochemistry, 1999
Abstract: Cyclophilin B (CyPB) is a cyclosporin A (CsA)‐binding protein mainly located in intracellular vesicles and secreted in biological fluids. In previous works, we demonstrated that CyPB interacts with T lymphocytes and enhances in vitro cellular incorporation and activity of CsA.
Carpentier, Mathieu   +8 more
openaire   +3 more sources

Cyclosporine inhibits a direct interaction between cyclophilins and hepatitis C NS5A.

open access: yesPLoS ONE, 2010
BackgroundHepatitis C Virus (HCV) infection is a leading indication for liver transplantation. HCV infection reoccurs almost universally post transplant, decreasing both graft longevity and patient survival.
Fiona Fernandes   +2 more
doaj   +1 more source

Alternative cell death pathways and cell metabolism [PDF]

open access: yes, 2013
While necroptosis has for long been viewed as an accidental mode of cell death triggered by physical or chemical damage, it has become clear over the last years that necroptosis can also represent a programmed form of cell death in mammalian cells.
Fulda, Simone
core   +2 more sources

SIV replication in human cells

open access: yesFrontiers in Microbiology, 2012
Current human immunodeficiency virus type 1 (HIV-1) pandemic is believed to originate from cross-species transmission of simian immunodeficiency virus (SIV) into human population.
Hiroaki eTakeuchi, Ryuta eSakuma
doaj   +1 more source

Structural and biochemical insights of CypA and AIF interaction [PDF]

open access: yes, 2017
The Cyclophilin A (CypA)/Apoptosis Inducing Factor (AIF) complex is implicated in the DNA degradation in response to various cellular stress conditions, such as oxidative stress, cerebral hypoxia-ischemia and traumatic brain injury.
Caporale, Andrea   +10 more
core   +1 more source

Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding [PDF]

open access: yesNew England Journal of Medicine, 2010
Osteogenesis imperfecta is a heritable disorder that causes bone fragility. Mutations in type I collagen result in autosomal dominant osteogenesis imperfecta, whereas mutations in either of two components of the collagen prolyl 3-hydroxylation complex (cartilage-associated protein [CRTAP] and prolyl 3-hydroxylase 1 [P3H1]) cause autosomal recessive ...
Aileen M, Barnes   +10 more
openaire   +2 more sources

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