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Deniz Torun

Showing results (11-20 of 24) with videos related to

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Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|January 4, 2014
Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/ThrombocythemiaDeniz Torun, Oral Nevruz, Mesut Akyol, et al.
Ophthalmic Genetics|November 28, 2009
A new syndrome associated with absence of lower lid lacrimal punctum, ptosis, elevation deficiency of both eyes and mild facial dysmorphismSefik Guran, Deniz Torun, Fatih Mehmet Mutlu, et al.
Journal of Molecular Psychiatry|February 26, 2015
Mitochondrial complex I and III gene mRNA levels in schizophrenia, and their relationship with clinical featuresSüleyman Akarsu, Deniz Torun, Abdullah Bolu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 19, 2020
Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathyAsburce Olgac, Cigdem Seher Kasapkara, Mustafa Kilic, et al.
Ophthalmic Genetics|January 14, 2017
Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control studyMehmet Talay Koylu, Murat Kucukevcilioglu, Fazil Cuneyt Erdurman, et al.
The Korean Journal of Internal Medicine|September 7, 2013
The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgerySedat Yilmaz, Hakan Erdem, Servet Tunay, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|February 23, 2018
Increased Endothelial Dysfunction and Insulin Resistance in Patients with Klinefelter SyndromeCem Haymana, Aydogan Aydogdu, Ibrahim Demirci, et al.
International Journal of Hematology|May 4, 2010
High frequency of MEFV gene mutations in patients with myeloid neoplasmCagatay Oktenli, Ozkan Sayan, Serkan Celik, et al.
Journal of Human Genetics|October 10, 2014
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in TurkeyAyşegül Ozantürk, Jan D Marshall, Gayle B Collin, et al.
The Journal of Clinical Investigation|January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish originYavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|January 4, 2014
Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/ThrombocythemiaDeniz Torun, Oral Nevruz, Mesut Akyol, et al.
Ophthalmic Genetics|November 28, 2009
A new syndrome associated with absence of lower lid lacrimal punctum, ptosis, elevation deficiency of both eyes and mild facial dysmorphismSefik Guran, Deniz Torun, Fatih Mehmet Mutlu, et al.
Journal of Molecular Psychiatry|February 26, 2015
Mitochondrial complex I and III gene mRNA levels in schizophrenia, and their relationship with clinical featuresSüleyman Akarsu, Deniz Torun, Abdullah Bolu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 19, 2020
Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathyAsburce Olgac, Cigdem Seher Kasapkara, Mustafa Kilic, et al.
Ophthalmic Genetics|January 14, 2017
Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control studyMehmet Talay Koylu, Murat Kucukevcilioglu, Fazil Cuneyt Erdurman, et al.
The Korean Journal of Internal Medicine|September 7, 2013
The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgerySedat Yilmaz, Hakan Erdem, Servet Tunay, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|February 23, 2018
Increased Endothelial Dysfunction and Insulin Resistance in Patients with Klinefelter SyndromeCem Haymana, Aydogan Aydogdu, Ibrahim Demirci, et al.
International Journal of Hematology|May 4, 2010
High frequency of MEFV gene mutations in patients with myeloid neoplasmCagatay Oktenli, Ozkan Sayan, Serkan Celik, et al.
Journal of Human Genetics|October 10, 2014
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in TurkeyAyşegül Ozantürk, Jan D Marshall, Gayle B Collin, et al.
The Journal of Clinical Investigation|January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish originYavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
Pageof 3