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PubMed 31772631 Effect of microRNA-133a-3p/matrix metalloproteinase-9 axis on the growth of atherosclerotic vascular smooth muscle cells. Atherosclerosis (AS) is the leading cause of cardiovascular disease and poses 1.87 KB 2020-11-03 1 130
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PubMed 31778855 A case of Birt-Hogg-Dubé syndrome implying reduced or no wild-type folliculin without mutated protein is pathogenic. Birt-Hogg-Dubé syndrome (BHDS) is an autosomal dominant cancer syndrome caused by a 1.49 KB 2020-12-03 2 77
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PubMed 31789978 Inherited conditions resulting in nephrolithiasis. PURPOSE OF REVIEW: Prevalence of pediatric urolithiasis is increasing, which is definitively visible in increasing numbers of presentations in emerge 1.45 KB 2020-12-03 1 46
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PubMed 31794795 TRPM2 ion channel is involved in the aggravation of cognitive impairment and down regulation of epilepsy threshold in pentylenetetrazole-induced kindling mice. Epilepsy is one of the most common neuro 1.98 KB 2020-12-03 1 125
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PubMed 31800874 Evaluation of the effect of topical and systemic ozone application in periodontitis: an experimental study in rats. OBJECTIVE: The goal of the present study was to determine the effect of systemic and 1.66 KB 2020-12-03 1 51
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PubMed 31808946 Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models. Since the first description of galactosemia in 1908 and despite decades of rese 2.12 KB 2020-07-28 1 105
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PubMed 31825161 A novel homozygous nonsense mutation of VPS13B associated with previously unreported features of Cohen syndrome. Cohen syndrome (CS) is a rare autosomal recessive disorder associated with mutations in 1.37 KB 2020-11-23 2 96
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PubMed 31843680 Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding osteopontin: The first digenic SIB 2.23 KB 2020-11-17 2 283
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PubMed 31936901 Unveiling the Molecular Basis of the Noonan Syndrome-Causing Mutation T42A of SHP2. Noonan syndrome (NS) is a genetic disorder caused by the hyperactivation of the RAS-MAPK molecular pathway. About 50 1.34 KB 2020-10-19 1 87
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PubMed 31981797 Cyclin-dependent kinase 1-mediated phosphorylation of protein kinase N1 promotes anchorage-independent growth and migration. Protein kinase N1 (PKN1) is a member of the protein kinase C superfamily. A 1.22 KB 2020-11-09 1 46
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