Search Results - "Kehinde, Elijah"
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Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract
Published in Kidney international (01-06-2014)“…Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately half of children with chronic kidney disease. CAKUT can be caused by…”
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Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract
Published in Journal of the American Society of Nephrology (01-01-2017)“…Congenital anomalies of the kidneys and urinary tract (CAKUT) are the leading cause of CKD in children, featuring a broad variety of malformations. A monogenic…”
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Combined ciprofloxacin and amikacin prophylaxis in the prevention of septicemia after transrectal ultrasound guided biopsy of the prostate
Published in The Journal of urology (01-03-2013)“…A steady increase in the incidence of septicemia after prostate biopsy in our unit between 2001 and 2005 prompted us to review our prophylactic antibiotic…”
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4
Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract
Published in Journal of the American Society of Nephrology (01-09-2014)“…Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately 40% of children with ESRD in the United States. Hitherto, mutations in…”
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5
Selenium Is Significantly Depleted Among Morbidly Obese Female Patients Seeking Bariatric Surgery
Published in Obesity surgery (01-11-2011)“…Background The aim of this study was to compare serum levels of trace elements in morbidly obese female patients seeking bariatric surgery with those of…”
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Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract
Published in Human genetics (01-08-2015)“…Congenital anomalies of the kidney and urinary tract (CAKUT) account for 40–50 % of chronic kidney disease that manifests in the first two decades of life…”
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7
Detection of Trichomonas vaginalis in prostate tissue and serostatus in patients with asymptomatic benign prostatic hyperplasia
Published in BMC infectious diseases (23-09-2016)“…Despite a worldwide common and progressive nature of benign prostate hyperplasia (BPH) in older men, no association has been observed between a causative…”
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Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis
Published in Kidney international (01-01-2012)“…Congenital abnormalities of the kidney and urinary tract (CAKUT) are the most frequent cause of chronic kidney disease in children, accounting for about half…”
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A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux
Published in PloS one (19-01-2018)“…Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause (40-50%) of chronic kidney disease (CKD) in children. About 40 monogenic…”
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10
They See a Rat, We Seek a Cure for Diseases: The Current Status of Animal Experimentation in Medical Practice
Published in Medical principles and practice (01-01-2013)“…The objective of this review article was to examine current and prospective developments in the scientific use of laboratory animals, and to find out whether…”
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Molecular basis for the effects of zinc deficiency on spermatogenesis: An experimental study in the Sprague-dawley rat model
Published in Indian journal of urology (01-01-2015)“…Introduction: The objective of this study is to investigate the molecular mechanisms underlying the effects of zinc deficiency on spermatogenesis in the…”
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A validated UPLC–MS/MS method for the analysis of linezolid and a novel oxazolidinone derivative (PH027) in plasma and its application to tissue distribution study in rabbits
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (01-01-2017)“…•UPLC–MS/MS method validation for two oxazolidinone antibiotics in plasma and tissues is reported.•Comparative study of the matrix effect during the analysis…”
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13
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Published in American journal of human genetics (06-08-2015)“…Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease in the first three decades of life…”
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14
Long term testicular ischemia–reperfusion injury-induced apoptosis: Involvement of survivin down-regulation
Published in Biochemical and biophysical research communications (07-05-2010)“…Testicular torsion is associated with damage to the testicular tissue as a result of ischemia–reperfusion injury (IRI) and induction of apoptosis leading to…”
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15
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract
Published in Nephrology, dialysis, transplantation (01-08-2016)“…Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney diseases in children and young adults, accounting for…”
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Comparative Pharmacokinetic Study for Linezolid and Two Novel Antibacterial Oxazolidinone Derivatives in Rabbits: Can Differences in the Pharmacokinetic Properties Explain the Discrepancies between Their In Vivo and In Vitro Antibacterial Activities?
Published in Pharmaceutics (07-09-2017)“…This is a comparative pharmacokinetics study of linezolid (Lzd), and two novel oxazolidinone antibacterial agents-PH027 and PH051-in rabbits to determine if…”
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17
Prostate cancer in Asia: A collaborative report
Published in Asian journal of urology (01-10-2014)“…The incidence of prostate cancer (PCa) within Asian population used to be much lower than in the Western population; however, in recent years the incidence and…”
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Response to the letter by Shailendra Kapoor: AMACR is an emerging diagnostic and prognostic tool in systemic malignancies
Published in International urology and nephrology (01-06-2013)Get full text
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Bone Healing and Hormonal Bioassay in Patients with Long-Bone Fractures and Concomitant Head Injury
Published in Medical principles and practice (01-01-2016)“…Objective: The aim of this study is to investigate healing of fractures in patients with concomitant head injuries and to measure blood hormone levels to…”
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A novel PKD1 variant demonstrates a disease-modifying role in trans with a truncating PKD1 mutation in patients with autosomal dominant polycystic kidney disease
Published in BMC nephrology (01-03-2015)“…Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common form of Polycystic Kidney Disease (PKD) and occurs at a frequency of 1/800 to 1/1000…”
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