Search Results - "Basak, F"
-
1
Microplastic ingestion and egestion by copepods in the Black Sea
Published in The Science of the total environment (01-02-2022)“…Ingestion and egestion of microplastics by copepods in the Black Sea was assessed for the first time. Composition and concentration of microplastics in the…”
Get full text
Journal Article -
2
Plastic occurrence in fish caught in the highly industrialized Gulf of İzmit (Eastern Sea of Marmara, Türkiye)
Published in Chemosphere (Oxford) (01-05-2023)“…Occurrence of micro- (<5 mm) and mesoplastics (5–25 mm) in twelve fish species caught off Gulf of İzmit in the Sea of Marmara was investigated. Plastics were…”
Get full text
Journal Article -
3
Addition of a general surgeon without addition of appropriate support is inadequate to improve outcomes of trauma patients in a rural setting: a cohort study of 1962 consecutive patients
Published in European journal of trauma and emergency surgery (Munich : 2007) (01-12-2017)“…Purpose Trauma care poses many challenges in small hospitals in rural settings. This report was designed to assess the role of a rural general surgeon with…”
Get full text
Journal Article -
4
Plastics in an endemic fish species (Alburnus sellal) and its parasite (Ligula intestinalis) in the Upper Tigris River, Türkiye
Published in The Science of the total environment (20-11-2023)“…Occurrence of micro-, meso- and macroplastics in Alburnus sellal and its parasite Ligula intestinalis is reported for the first time in the Tigris River, one…”
Get full text
Journal Article -
5
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents
Published in Human genetics (01-08-2016)“…Hearing loss is the most common sensory deficit in humans with causative variants in over 140 genes. With few exceptions, however, the population-specific…”
Get full text
Journal Article -
6
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice
Published in Proceedings of the National Academy of Sciences - PNAS (24-05-2016)“…Hair cells of the inner ear, the mechanosensory receptors, convert sound waves into neural signals that are passed to the brain via the auditory nerve. Little…”
Get full text
Journal Article -
7
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing
Published in Proceedings of the National Academy of Sciences - PNAS (08-07-2014)“…In a large consanguineous Turkish kindred with recessive nonsyndromic, prelingual, profound hearing loss, we identified in the gene FAM65B (MIM611410) a splice…”
Get full text
Journal Article -
8
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort
Published in Genetics in medicine (01-04-2016)“…Autosomal recessive nonsyndromic deafness (ARNSD) is characterized by a high degree of genetic heterogeneity, with reported mutations in 58 different genes…”
Get full text
Journal Article -
9
SLITRK6 mutations cause myopia and deafness in humans and mice
Published in The Journal of clinical investigation (01-05-2013)“…Myopia is by far the most common human eye disorder that is known to have a clear, albeit poorly defined, heritable component. In this study, we describe an…”
Get full text
Journal Article -
10
Antimicrobial Effect of Toothpastes Containing Fluoride, Xylitol, or Xylitol-Probiotic on Salivary Streptococcus mutans and Lactobacillus in Children
Published in Nigerian journal of clinical practice (01-02-2018)“…Aim: This in vivo study was designed to compare the antimicrobial effect of toothpastes containing fluoride, xylitol, or xylitol-probiotic on Streptococcus…”
Get full text
Journal Article -
11
Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey
Published in Genetic testing and molecular biomarkers (01-01-2011)“…More than 60% of prelingual deafness is genetic in origin, and of these up to 95% are monogenic autosomal recessive traits. Causal mutations have been…”
Get more information
Journal Article -
12
Incidental findings during routine pathological evaluation of gallbladder specimens: review of 1,747 elective laparoscopic cholecystectomy cases
Published in Annals of the Royal College of Surgeons of England (01-04-2016)“…Introduction Cholecystectomy for benign gallbladder diseases can lead to previously undiagnosed gallbladder cancer during histopathological evaluation. Despite…”
Get full text
Journal Article -
13
Glisson's capsule cauterisation is associated with increased postoperative pain after laparoscopic cholecystectomy: a prospective case-control study
Published in Annals of the Royal College of Surgeons of England (01-07-2017)“…INTRODUCTION Postoperative pain after laparoscopic cholecystectomy has three components: parietal, visceral and referred pain felt at the shoulder. Visceral…”
Get full text
Journal Article -
14
The In vitro Evaluation of the effect of xyliwhite, probiotic, and the conventional toothpastes on the enamel roughness and microhardness
Published in Nigerian journal of clinical practice (01-03-2018)“…Aim: The aim of this study was to evaluate the effect of fluoride, Xylitol, Probiotic, and Whitening toothpastes on the permanent teeth enamel roughness and…”
Get full text
Journal Article -
15
Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil
Published in Annals of human genetics (01-11-2016)“…Summary Identifying the genetic etiology in a person with hearing loss (HL) is challenging due to the extreme genetic heterogeneity in HL and the…”
Get full text
Journal Article -
16
Recurrent and private MYO15A mutations are associated with deafness in the Turkish population
Published in Genetic testing and molecular biomarkers (01-08-2010)“…The identities and frequencies of MYO15A mutations associated with hearing loss in different populations remained largely unknown. We screened the MYO15A gene…”
Get more information
Journal Article -
17
Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients
Published in Pediatric nephrology (Berlin, West) (01-08-2006)“…Mutations in the NPHS2 gene are a frequent cause of familial and sporadic steroid-resistant nephrotic syndrome (SRNS). Inter-ethnic differences have also been…”
Get full text
Journal Article -
18
Evolution-based algorithm for the management of penetrating abdominal stab injury
Published in European journal of trauma and emergency surgery (Munich : 2007) (01-10-2012)“…Purpose As an increasing amount of penetrating abdominal stab injuries has been observed in the last few decades, it is important to evaluate the adequacy of…”
Get full text
Journal Article -
19
Multiple Intestinal Intussusceptions in Peutz-Jeghers' Syndrome: a Case Report
Published in Acta chirurgica belgica (2010)“…Peutz-Jeghers' syndrome (PJS) is an autosomal dominant inherited disease, which is characterized by mucocutaneus pigmentation and hamartomatous…”
Get full text
Journal Article -
20
Treatment of space loss caused by submerged maxillary second primary molar
Published in Journal of the Indian Society of Pedodontics and Preventive Dentistry (01-03-2007)“…Submersion is a clinical term describing a tooth depressed below the occlusal plane. In this case report, we present the treatment of a patient who had totally…”
Get full text
Journal Article