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GLCCI1 encodes a protein of unknown function. Additionally we are shipping GLCCI1 Proteins (2) and many more products for this protein.
Showing 10 out of 56 products:
Human Polyclonal GLCCI1 Primary Antibody for EIA, IHC (p) - ABIN952521
Miazek, Malissen: Two genes, three messengers: hybrid transcript between a gene expressed at specific stages of T-cell and sperm maturation and an unrelated adjacent gene. in Immunogenetics 2003
Show all 4 references for ABIN952521
Human Polyclonal GLCCI1 Primary Antibody for EIA, WB - ABIN952522
Olsen, Blagoev, Gnad, Macek, Kumar, Mortensen, Mann: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. in Cell 2006
Show all 4 references for ABIN952522
Glcci1 promotes the normal development and maintenance of podocyte structure and function.
Carriers of the GLCCI1-C allele had lower levels of baseline rheumatoid arthritis disease activity, suggesting a role for the GLCCI1 gene in regulation of glucocorticoid sensitivity to endogenously produced cortisol.
Carriers of the rs41423247 GLCCI1 polymorphism had a higher probability of responding to glucocorticoids, whereas all other polymorphisms did not affect the likelihood of response to treatment of graft-versus-host disease patients.
GLCCI1 rs37972 T allele was not significantly associated with an increased risk of oral corticosteroid use.
GLCCI1 variant accelerates pulmonary function decline in patients with asthma receiving inhaled corticosteroids.
Novel association was found between intraocular pressure and a common variant at 7p21 near to GLCCI1 and ICA1 (show ICA1 Antibodies).
GLCCI1 rs37973 does not influence treatment response to inhaled corticosteroids in white subjects with asthma.
Studied the influence of GLCCI1 SNP rs37972 on dexamethasone efficacy in bacterial meningitis patients.Results show rs37972 in GLCCI1 is associated with death in patients with CA bacterial meningitis treated with adjunctive dexamethasone therapy.
GLCCI1 nucleotide polymorphisms associated with steroid-responsiveness in asthmatic patients are unlikely to have a clinically actionable impact in pediatric nephrotic syndrome.
Variation at GLCCI1 and FCER2 (show FCER2 Antibodies) could lead personalized asthma treatment.
A functional GLCCI1 variant is associated with substantial decrements in the response to inhaled glucocorticoids in patients with asthma.
This gene encodes a protein of unknown function. Expression of this gene is induced by glucocorticoids and may be an early marker for glucocorticoid-induced apoptosis. Single nucleotide polymorphisms in this gene are associated with a decreased response to inhaled glucocorticoids in asthmatic patients.
glucocorticoid-induced gene 18 protein
, glucocorticoid-induced transcript 1 protein
, thymocyte/spermatocyte selection 1
, thymocyte/spermatocyte selection protein 1
, glucocorticoid induced transcript 1