Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Science of the Total Environment|July 23, 2023
Plastics in an endemic fish species (Alburnus sellal) and its parasite (Ligula intestinalis) in the Upper Tigris River, TürkiyeÜlgen Aytan, F Basak Esensoy, Esra Arifoğlu, et al.
European Journal of Trauma and Emergency Surgery : Official Publication of the European Trauma Society|January 28, 2016
Evolution-based algorithm for the management of penetrating abdominal stab injuryO Alimoglu, M Yucel, I E Subasi, et al.
Annals of the Royal College of Surgeons of England|March 1, 2016
Incidental findings during routine pathological evaluation of gallbladder specimens: review of 1,747 elective laparoscopic cholecystectomy casesF Basak, M Hasbahceci, T Canbak, et al.
Annals of the Royal College of Surgeons of England|June 30, 2017
Glisson's capsule cauterisation is associated with increased postoperative pain after laparoscopic cholecystectomy: a prospective case-control studyF Basak, M Hasbahceci, A Sisik, et al.
Genetic Testing and Molecular Biomarkers|July 21, 2010
Recurrent and private MYO15A mutations are associated with deafness in the Turkish populationF Basak Cengiz, Duygu Duman, Asli Sirmaci, et al.
Annals of Human Genetics|November 22, 2016
Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern BrazilGabrielle N Manzoli, Guney Bademci, Angelina X Acosta, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2016
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and miceOscar Diaz-Horta, Clemer Abad, Levent Sennaroglu, et al.
The Journal of Clinical Investigation|April 2, 2013
SLITRK6 mutations cause myopia and deafness in humans and miceMustafa Tekin, Barry A Chioza, Yoshifumi Matsumoto, et al.
Human Genetics|June 27, 2016
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continentsDenise Yan, Demet Tekin, Guney Bademci, et al.
Pageof 3