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Nejat Akar

Showing results (171-180 of 229) with videos related to

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Pediatric Hematology and Oncology|August 7, 2009
Soluble endothelial protein C receptor level in children with sepsisTanil Kendirli, Erdal Ince, Ergin Ciftci, et al.
Molecular Biology Reports|August 12, 2009
Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemiaErkan Yilmaz, Rüçhan Akar, Serap Tiraş Eker, et al.
Immunity, Inflammation and Disease|April 27, 2023
Behçet syndrome: The disturbed balance between anti- (CLEC12A, CLC) and proinflammatory (IFI27) gene expressionsAli Kemal Oğuz, Çağdaş Şahap Oygür, Seda Taşır, et al.
Microbial Drug Resistance (Larchmont, N.Y.)|January 15, 2005
Sequence analysis of rpoB mutations in rifampin-resistant clinical Mycobacterium tuberculosis isolates from TurkeyZeynep Ceren Karahan, Figen Atalay, Meltem Uzun, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|December 17, 2009
Association of the tumor necrosis factor-alpha -308 G/A polymorphism with nasal polyposisHunkar Batikhan, Mustafa Kursat Gokcan, Esen Beder, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 8, 2008
Soluble endothelial protein C receptor levels in Behçet patients with and without ocular involvementF Nilüfer Yalçindağ, Figen Batioğlu, Ozden Ozdemir, et al.
Journal of Thrombosis and Thrombolysis|March 20, 2009
Soluble endothelial protein C receptor levels in healthy populationFiliz Simsek Orhon, Huseyin Ergun, Yonca Egin, et al.
Human Mutation|April 4, 2003
Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative matingMustafa Tekin, Türker Duman, Gönül Boğoçlu, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotypeMustafa Tekin, Asli Kavaz, Merih Berberoğlu, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 14, 2012
Prohemostatic and antithrombin activities of Ankaferd hemostat are linked to fibrinogen gamma chain and prothrombin by functional proteomic analysesDuygu Ozel-Demiralp, Nasit Igci, Beycan Ayhan, et al.
Pageof 23

Showing results (171-180 of 229) with videos related to

Sort By:
Pageof 23
Pediatric Hematology and Oncology|August 7, 2009
Soluble endothelial protein C receptor level in children with sepsisTanil Kendirli, Erdal Ince, Ergin Ciftci, et al.
Molecular Biology Reports|August 12, 2009
Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemiaErkan Yilmaz, Rüçhan Akar, Serap Tiraş Eker, et al.
Immunity, Inflammation and Disease|April 27, 2023
Behçet syndrome: The disturbed balance between anti- (CLEC12A, CLC) and proinflammatory (IFI27) gene expressionsAli Kemal Oğuz, Çağdaş Şahap Oygür, Seda Taşır, et al.
Microbial Drug Resistance (Larchmont, N.Y.)|January 15, 2005
Sequence analysis of rpoB mutations in rifampin-resistant clinical Mycobacterium tuberculosis isolates from TurkeyZeynep Ceren Karahan, Figen Atalay, Meltem Uzun, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|December 17, 2009
Association of the tumor necrosis factor-alpha -308 G/A polymorphism with nasal polyposisHunkar Batikhan, Mustafa Kursat Gokcan, Esen Beder, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 8, 2008
Soluble endothelial protein C receptor levels in Behçet patients with and without ocular involvementF Nilüfer Yalçindağ, Figen Batioğlu, Ozden Ozdemir, et al.
Journal of Thrombosis and Thrombolysis|March 20, 2009
Soluble endothelial protein C receptor levels in healthy populationFiliz Simsek Orhon, Huseyin Ergun, Yonca Egin, et al.
Human Mutation|April 4, 2003
Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative matingMustafa Tekin, Türker Duman, Gönül Boğoçlu, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotypeMustafa Tekin, Asli Kavaz, Merih Berberoğlu, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 14, 2012
Prohemostatic and antithrombin activities of Ankaferd hemostat are linked to fibrinogen gamma chain and prothrombin by functional proteomic analysesDuygu Ozel-Demiralp, Nasit Igci, Beycan Ayhan, et al.
Pageof 23