Results 81 to 90 of about 2,702,233 (230)
Reduction of malignant phenotype of HEPG2 cell is associated with the expression of connexin 26 but not connexin 32 [PDF]
Carcinogenesis, 2001 Connexin (Cx) genes have a negative growth effect on tumour cells with certain specificity. However, it is not clear whether each Cx gene can act similarly in growth control. Hepatocytes normally express Cx26 and Cx32 as their major gap junction genes, but HepG2 cells, a hepatoma cell line, are deficient in gap junctional intercellular communication ...
T, Yano +3 more
openaire +2 more sources
Andrology, EarlyView.ABSTRACT Background Challenges in establishing clinical conventional in vitro fertilization (IVF) in horses include variation in sperm and oocyte quality, which can be affected by mare age. Extended preincubation of stallion spermatozoa has resulted in successful IVF.
Raul A. Gonzalez‐Castro +6 more
wiley +1 more source
, 2013 Hintergrund: Ein nicht-syndromaler isolierter Hörverlust ist der häufigste angeborene Defekt bei Neugeborenen. Etwa eines von 500-1000 Neugeborenen ist bereits bei der Geburt oder in den ersten beiden Lebensjahren von einer hochgradigen Hörstörung ...
Birkenhäger, R +5 more
core +1 more source
Andrology, EarlyView.ABSTRACT Background Pro‐inflammatory cytokines, TNF and IL‐1B, are essential for testicular homeostasis. Diacerein, an anti‐inflammatory drug, inhibits these cytokines, impairing M2 macrophages and Leydig cells (LCs). However, its impact on Sertoli cells (SCs) and M1 (CD68) macrophages remains unknown.
Elide Loise Freitas de Jesus +6 more
wiley +1 more source
Connexin 36 as a Regulator of Consummatory Behaviour [PDF]
, 2014 Gap junctions enable metabolic and electrical coupling of adjacent cells. Connexin 36 (Cx36) is a gap junction protein found predominantly in mammalian neurons.
Christian, David
core
The prevalence of Connexin 26 mutations in the Swedish population
, 2005 Mutations in GJB2, the gene encoding the protein Connexin 26, have been shown to account for as much as 50% of autosomal recessive, non-syndromic childhood hearing loss (ARNSHL).
Hederstierna, Christina +4 more
core +1 more source
Vohwinkel Syndrome secondary to missense mutation D66H in GJB2 gene (connexin 26) can include epileptic manifestations [PDF]
, 2010 Vohwinkel Syndrome (VS) is a type of diffuse hereditary palmoplantar keratodermas (DHPPK) accompanied by skeletal dimorphisms and sensorineural deafness.
Fernandez, Cristina Naranjo +3 more
core +1 more source
British Journal of Pharmacology, EarlyView.Background and Purpose Notoginsenoside‐Fa (Noto‐Fa) is an emerging active compound derived from notoginseng with promise in treating cardiovascular diseases. The development of cardiovascular diseases is intricately linked to the damage of vascular endothelium and it is widely acknowledged that numerous chronic inflammation pathways, especially the ...
Xiao‐Ying Yu +9 more
wiley +1 more source
Discover Mental HealthObjective To investigate changed levels of serum astrocytic biomarkers, including glial cell line-derived neurotrophic factor (GDNF), aldehyde dehydrogenase (ALDH) and connexin-26, and the correlations with depression subtypes, cognitive dysfunction and ...
Zi-Jie Ma +7 more
doaj +1 more source
Correlation between audiometric data and the 35delG mutation in ten patients
Brazilian Journal of Otorhinolaryngology, 2007 Summary: Mutations in the connexin 26 gene seem to be extremely common in non-syndromic hereditary deafness genesis, especially the 35delG, but there are still only a few studies that describe the audiometric characteristics of patients with these ...
Vânia Belintani Piatto +5 more
doaj +1 more source