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Bekir Erguner

Showing results (1-10 of 6) with videos related to

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Performance comparison of Next Generation sequencing platformsBekir Erguner, Duran Ustek, Mahmut S Sagiroglu
Genome Informatics. International Conference on Genome Informatics|November 15, 2011
Characterizing common substructures of ligands for GPCR protein subfamiliesBekir Erguner, Masahiro Hattori, Susumu Goto, et al.
European Journal of Medical Genetics|September 18, 2016
A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetusMehmet Burak Mutlu, Arda Cetinkaya, Nermin Koc, et al.
Genome Announcements|June 11, 2016
Draft Genome Sequences of Two Heat-Resistant Mutant Strains (A52 and B41) of the Photosynthetic Hydrogen-Producing Bacterium Rhodobacter capsulatusAbdulmecit Gokce, Zeynep Petek Cakar, Meral Yucel, et al.
BMC Genetics|October 1, 2013
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtypeFatih Bayrakli, Bulent Guclu, Cengiz Yakicier, et al.
Journal of Human Genetics|October 2, 2015
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 geneFatih Bayrakli, Hatice Gamze Poyrazoglu, Sirin Yuksel, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Performance comparison of Next Generation sequencing platformsBekir Erguner, Duran Ustek, Mahmut S Sagiroglu
Genome Informatics. International Conference on Genome Informatics|November 15, 2011
Characterizing common substructures of ligands for GPCR protein subfamiliesBekir Erguner, Masahiro Hattori, Susumu Goto, et al.
European Journal of Medical Genetics|September 18, 2016
A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetusMehmet Burak Mutlu, Arda Cetinkaya, Nermin Koc, et al.
Genome Announcements|June 11, 2016
Draft Genome Sequences of Two Heat-Resistant Mutant Strains (A52 and B41) of the Photosynthetic Hydrogen-Producing Bacterium Rhodobacter capsulatusAbdulmecit Gokce, Zeynep Petek Cakar, Meral Yucel, et al.
BMC Genetics|October 1, 2013
Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtypeFatih Bayrakli, Bulent Guclu, Cengiz Yakicier, et al.
Journal of Human Genetics|October 2, 2015
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 geneFatih Bayrakli, Hatice Gamze Poyrazoglu, Sirin Yuksel, et al.
Pageof 1