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anti-Human PDE7B Anticorps:
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Human Polyclonal PDE7B Primary Antibody pour ELISA, IP - ABIN2747203
Petersen, Kristensen, Jeppesen, Grøndahl, Wissing, Macklon, Andersen: Distribution and function of 3',5'-Cyclic-AMP phosphodiesterases in the human ovary. dans Molecular and cellular endocrinology 2015
We have identified three novel loci (PDE7B, UBL3, and a new independent marker in CDKN2B-AS1) associated with BRCAX, and replicated previously reported SNPs (24 of 92) and moderate/high-penetrance (seven of 23) genes for Korean BRCAX. For the novel candidate loci, evidence supported their roles in regulatory function
both low miR-200c and high PDE7B expression were correlated with poor survival of breast cancer patients. Our study supports a critical role of miR-200c/PDE7B relationship in triple-negative breast cancer tumorigenesis.
PDE7B polymorphisms were not associated with schizophrenia risk.
higher expression of PDE7B might be a novel unfavorable prognostic indicator in MCL, which possess important clinical significance.
PDE7B mRNA expression is obviously higher in mantle cell lymphoma patients compared with normal controls and significantly correlates with unfavorable cytogenetic characteristics.
The low frequency of this 5' untranslated region variant indicates that it does not explain the higher PDE7B expression in patients with chronic lymphocytic leukemia (CLL) but it has the potential to influence other settings that involve a role for PDE7B.
High PDE7B is associated with chronic lymphocytic leukemia.
Genetic variation in the phosphodiesterase 7B is associated with bioavailability of testosterone enanthate.
As a first exploitation of this unique cohort, we identify three novel candidate dyslexia genes, ZNF280D and TCF12 at 15q21, and PDE7B at 6q23.3, by molecular mapping of the familial translocation with the 15q21 breakpoint.
higher levels than in normal B-cell of PDE7B are found in chronic lymphocytic leukemia
It is one of the enzymes responsible for controlling specifically the intracellular levels of cyclic adenosine 3', 5'-monophosphate in the immune and central nervous systems.
For the first time, it was demonstrated that the deletion of the PDE7B gene or the pharmacological inhibition of PDE7A and -B had no effect on ovalbumin-induced airway inflammation and airway hyperreactivity.
The 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a cAMP-specific phosphodiesterase, a member of the cyclic nucleotide phosphodiesterase family.
, cAMP-specific 3',5'-cyclic phosphodiesterase 7B-like
, cyclic nucleotide phosphodiesterase 7b
, cAMP-specific 3',5'-cyclic phosphodiesterase 7B
, high-affinity cAMP-specific 3',5'-cyclic phosphodiesterase
, rolipram-insensitive phosphodiesterase type 7