نتایج جستجو برای: dpp6
تعداد نتایج: 82 فیلتر نتایج به سال:
Studies are being conducted on the applicability of genomic data to improve the accuracy of the selection process in livestock, and genome-wide association studies (GWAS) provide valuable information to enhance the understanding on the genetics of complex traits. The aim of this study was to identify genomic regions and genes that play roles in birth weight (BW), weaning weight adjusted for 210...
Sphingolipid long-chain bases and their phosphorylated derivatives, for example, sphingosine-1-phosphate in mammals, have been implicated as signaling molecules. The possibility that Saccharomyces cerevisiae cells also use long-chain-base phosphates to regulate cellular processes has only recently begun to be examined. Here we present a simple and sensitive procedure for analyzing and quantifyi...
A myotrophic lateral sclerosis (ALS) is an adultonset neurodegenerative disease characterized by progressive loss of motor neurons from the spinal cord, brainstem, and cerebral cortex that typically results in death 2 to 5 years following onset. Approximately 10% of patients with ALS have a family history, of which 15% to 20% are linked to mutations in the SOD1 gene; these patients most frequen...
Background: Familial cascade screening is well established in patients with heritable cardiac disease and cases of sudden arrhythmic death syndrome. The clinical benefit family idiopathic ventricular fibrillation (IVF) unknown. Methods: Patients IVF were identified from national institutional registries. All underwent systematic comprehensive evaluation to exclude identifiable causes arrest a m...
Abstract Introduction The subcutaneous implantable cardioverter-defibrillator (S-ICD) is considered especially beneficial in young patients with an inherited cardiac disease, but data on these patient groups limited. Purpose To evaluate the eligibility of disease for therapy a Methods We retrospectively analysed all who received S-ICD our tertiary center between February 2009 and June 2021. ECG...
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive limb or bulbar weakness. Efforts to elucidate the disease-associated loci have to date produced conflicting results. One strategy to improve power in genome-wide studies is to genotype a genetically homogenous population. Such a population exhibits extended linkage disequilibrium (LD) and lower...
The mouse rump white (Rw) mutation causes a pigmentation defect in heterozygotes and embryonic lethality in homozygotes. At embryonic day (E) 7.5, Rw/Rw embryos are retarded in growth, fail to complete neurulation and die around E 9.5. The Rw mutation is associated with a chromosomal inversion spanning 30 cM of the proximal portion of mouse chromosome 5. The Rw embryonic lethality is complement...
RefeRences Birnbaum, S. G., Varga, A. W., Yuan, L. L., Anderson, A. E., Sweatt, J. D., and Schrader, L. A. (2004). Structure and function of Kv4-family transient potassium channels. Physiol. Rev. 84, 803–833. Clark, B. D., Kwon, E., Maffie, J., Jeong, H. Y., Nadal, M., Strop, P., and Rudy, B. (2008). DPP6 localization in brain supports function as a Kv4 channel associated protein. Front. Mol. N...
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