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Mehmet Bugrahan Duz

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Neurocase|October 22, 2021
A novel CLN5 mutation in Turkish patient with variant late-onset neuronal ceroid lipofuscinosis and recurrent fractures that causes severe morbidityMehmet Bugrahan Duz
Clinical Dysmorphology|July 9, 2020
Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature reviewMehmet Bugrahan Duz, Ali Topak
Molecular Biology Reports|January 28, 2021
Differential expression of ABCB1, ABCG2, and KLF4 as putative indicators for paclitaxel resistance in human epithelial type 2 cellsMehmet Bugrahan Duz, Omer Faruk Karatas
Journal of Human Genetics|October 23, 2020
Analysis of rearrangements of the CFTR gene in patients from Turkey with CFTR-related disorders: frequent exon 2 deletionMehmet Bugrahan Duz, Pelin Ozyavuz Cubuk
Pediatric Research|July 13, 2026
Perspectives on genomic newborn screening studies: design, implementation, and outcomesMehmet Bugrahan Duz, Wendy K Chung
Molecular Biology Reports|July 7, 2020
Expression profile of stem cell markers and ABC transporters in 5-fluorouracil resistant Hep-2 cellsMehmet Bugrahan Duz, Omer Faruk Karatas
European Journal of Medical Genetics|September 16, 2021
Acrocapitofemoral dysplasia: Novel mutation in IHH in two adult patients from the third family in the literature and progression of the diseasePelin Ozyavuz Cubuk, Mehmet Bugrahan Duz
Global Medical Genetics|February 16, 2022
Rare Findings in Cleidocranial Dysplasia Caused by RUNX MutationAysel Kalayci Yigin, Mehmet Bugrahan Duz, Mehmet Seven
Future Oncology (London, England)|June 20, 2014
The role of miRNAs in cancer: from pathogenesis to therapeutic implicationsMehmet Seven, Omer Faruk Karatas, Mehmet Bugrahan Duz, et al.
Molecular Syndromology|May 13, 2026
<i>CHAMP1</i>-Related Neurodevelopmental Disorder: Two Turkish Cases with Novel Truncating Variants and Literature ReviewZehra Manav Yigit, Pelin Ozyavuz Cubuk, Kamil Utku Bayrak, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Neurocase|October 22, 2021
A novel CLN5 mutation in Turkish patient with variant late-onset neuronal ceroid lipofuscinosis and recurrent fractures that causes severe morbidityMehmet Bugrahan Duz
Clinical Dysmorphology|July 9, 2020
Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature reviewMehmet Bugrahan Duz, Ali Topak
Molecular Biology Reports|January 28, 2021
Differential expression of ABCB1, ABCG2, and KLF4 as putative indicators for paclitaxel resistance in human epithelial type 2 cellsMehmet Bugrahan Duz, Omer Faruk Karatas
Journal of Human Genetics|October 23, 2020
Analysis of rearrangements of the CFTR gene in patients from Turkey with CFTR-related disorders: frequent exon 2 deletionMehmet Bugrahan Duz, Pelin Ozyavuz Cubuk
Pediatric Research|July 13, 2026
Perspectives on genomic newborn screening studies: design, implementation, and outcomesMehmet Bugrahan Duz, Wendy K Chung
Molecular Biology Reports|July 7, 2020
Expression profile of stem cell markers and ABC transporters in 5-fluorouracil resistant Hep-2 cellsMehmet Bugrahan Duz, Omer Faruk Karatas
European Journal of Medical Genetics|September 16, 2021
Acrocapitofemoral dysplasia: Novel mutation in IHH in two adult patients from the third family in the literature and progression of the diseasePelin Ozyavuz Cubuk, Mehmet Bugrahan Duz
Global Medical Genetics|February 16, 2022
Rare Findings in Cleidocranial Dysplasia Caused by RUNX MutationAysel Kalayci Yigin, Mehmet Bugrahan Duz, Mehmet Seven
Future Oncology (London, England)|June 20, 2014
The role of miRNAs in cancer: from pathogenesis to therapeutic implicationsMehmet Seven, Omer Faruk Karatas, Mehmet Bugrahan Duz, et al.
Molecular Syndromology|May 13, 2026
<i>CHAMP1</i>-Related Neurodevelopmental Disorder: Two Turkish Cases with Novel Truncating Variants and Literature ReviewZehra Manav Yigit, Pelin Ozyavuz Cubuk, Kamil Utku Bayrak, et al.
Pageof 2