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Mustafa Dogan

Showing results (71-80 of 96) with videos related to

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International Journal of Molecular Sciences|January 28, 2026
Biallelic Truncating <i>DNAH14</i> Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature ReviewSavas Baris, Mustafa Dogan, Kerem Terali, et al.
The Tohoku Journal of Experimental Medicine|December 2, 2004
Plasma leptin levels in rats with pancreatitisNihat Yavuz, Ethem Unal, Kemal Memisoglu, et al.
Molecular Syndromology|February 15, 2024
A Deeper Insight into <i>COL4A3</i>, <i>COL4A4</i>, and <i>COL4A5</i> Variants and Genotype-Phenotype Correlation of a Turkish Cohort with Alport SyndromeCuneyd Yavas, Nehir Ozdemir Ozgenturk, Mustafa Dogan, et al.
Clinical Nephrology|April 23, 2026
Evaluation of epicardial adipose tissue in children with chronic kidney diseaseMehmet Baha Aytac, Mustafa Dogan, Sule Ayas Ergul, et al.
Brain & Development|July 9, 2025
Biallelic novel CCDC186 loss-of-function variant disrupting the gene function causes neurodevelopmental phenotype and review of the literatureAlper Gezdirici, Sultan Buse Turk, Tuna Eren Esen, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 7, 2014
Evaluation of ovarian reserve in Hashimoto's thyroiditisAbdullah Tuten, Esra Hatipoglu, Mahmut Oncul, et al.
Molecular Syndromology|January 7, 2026
Molecular and Clinical Profiles of Patients with RASopathies: Targeted Next-Generation Sequencing Panel Results and Identification of 14 Novel Disease-Causing VariantsKubra Ates, Murat Ozturk, Zeynep Esener, et al.
Forensic Science International. Genetics|May 21, 2021
Genetic relationships of Southwest Asian and Mediterranean populationsKenneth K Kidd, Ozlem Bulbul, Cemal Gurkan, et al.
Life (Basel, Switzerland)|March 28, 2026
Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney DiseasesSavas Baris, Kerem Terali, Serdar Bozlak, et al.
SAGE Open Medicine|April 25, 2022
A 5-year surveillance of healthcare-associated infections in a university hospital: A retrospective analysisIlknur Erdem, Ilker Yıldırım, Birol Safak, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
International Journal of Molecular Sciences|January 28, 2026
Biallelic Truncating <i>DNAH14</i> Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature ReviewSavas Baris, Mustafa Dogan, Kerem Terali, et al.
The Tohoku Journal of Experimental Medicine|December 2, 2004
Plasma leptin levels in rats with pancreatitisNihat Yavuz, Ethem Unal, Kemal Memisoglu, et al.
Molecular Syndromology|February 15, 2024
A Deeper Insight into <i>COL4A3</i>, <i>COL4A4</i>, and <i>COL4A5</i> Variants and Genotype-Phenotype Correlation of a Turkish Cohort with Alport SyndromeCuneyd Yavas, Nehir Ozdemir Ozgenturk, Mustafa Dogan, et al.
Clinical Nephrology|April 23, 2026
Evaluation of epicardial adipose tissue in children with chronic kidney diseaseMehmet Baha Aytac, Mustafa Dogan, Sule Ayas Ergul, et al.
Brain & Development|July 9, 2025
Biallelic novel CCDC186 loss-of-function variant disrupting the gene function causes neurodevelopmental phenotype and review of the literatureAlper Gezdirici, Sultan Buse Turk, Tuna Eren Esen, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 7, 2014
Evaluation of ovarian reserve in Hashimoto's thyroiditisAbdullah Tuten, Esra Hatipoglu, Mahmut Oncul, et al.
Molecular Syndromology|January 7, 2026
Molecular and Clinical Profiles of Patients with RASopathies: Targeted Next-Generation Sequencing Panel Results and Identification of 14 Novel Disease-Causing VariantsKubra Ates, Murat Ozturk, Zeynep Esener, et al.
Forensic Science International. Genetics|May 21, 2021
Genetic relationships of Southwest Asian and Mediterranean populationsKenneth K Kidd, Ozlem Bulbul, Cemal Gurkan, et al.
Life (Basel, Switzerland)|March 28, 2026
Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney DiseasesSavas Baris, Kerem Terali, Serdar Bozlak, et al.
SAGE Open Medicine|April 25, 2022
A 5-year surveillance of healthcare-associated infections in a university hospital: A retrospective analysisIlknur Erdem, Ilker Yıldırım, Birol Safak, et al.
Pageof 10