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Serdar Coskun

Showing results (51-60 of 59) with videos related to

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Pharmaceuticals (Basel, Switzerland)|June 1, 2023
Antigen Unmasking Is Required to Clinically Assess Levels and Localisation Patterns of Phospholipase C Zeta in Human SpermJunaid Kashir, Bhavesh V Mistry, Lujain BuSaleh, et al.
European Journal of Medical Genetics|September 16, 2008
Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemiaNamik Kaya, Mohammad Al-Owain, Albandary Albakheet, et al.
Andrology|April 17, 2020
Phospholipase C zeta profiles are indicative of optimal sperm parameters and fertilisation success in patients undergoing fertility treatmentJunaid Kashir, Bhavesh V Mistry, Lujain BuSaleh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2008
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan diseaseNamik Kaya, Faiqa Imtiaz, Dilek Colak, et al.
Journal of Experimental & Clinical Assisted Reproduction|August 30, 2007
Regional clinical practice patterns in reproductive endocrinology: a collaborative transnational pilot survey of in vitro fertilization programs in the Middle EastEric Scott Sills, Hussein S Qublan, Zeev Blumenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
A genomics approach to male infertilityNaif Alhathal, Sateesh Maddirevula, Serdar Coskun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitroSenthilkumar A Natesan, Alex J Bladon, Serdar Coskun, et al.
Med (New York, N.Y.)|November 6, 2024
Arab founder variants: Contributions to clinical genomics and precision medicineLama AlAbdi, Sateesh Maddirevula, Bayan Aljamal, et al.
Acta Neuropathologica|December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseasesElena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Pharmaceuticals (Basel, Switzerland)|June 1, 2023
Antigen Unmasking Is Required to Clinically Assess Levels and Localisation Patterns of Phospholipase C Zeta in Human SpermJunaid Kashir, Bhavesh V Mistry, Lujain BuSaleh, et al.
European Journal of Medical Genetics|September 16, 2008
Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemiaNamik Kaya, Mohammad Al-Owain, Albandary Albakheet, et al.
Andrology|April 17, 2020
Phospholipase C zeta profiles are indicative of optimal sperm parameters and fertilisation success in patients undergoing fertility treatmentJunaid Kashir, Bhavesh V Mistry, Lujain BuSaleh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2008
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan diseaseNamik Kaya, Faiqa Imtiaz, Dilek Colak, et al.
Journal of Experimental & Clinical Assisted Reproduction|August 30, 2007
Regional clinical practice patterns in reproductive endocrinology: a collaborative transnational pilot survey of in vitro fertilization programs in the Middle EastEric Scott Sills, Hussein S Qublan, Zeev Blumenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
A genomics approach to male infertilityNaif Alhathal, Sateesh Maddirevula, Serdar Coskun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitroSenthilkumar A Natesan, Alex J Bladon, Serdar Coskun, et al.
Med (New York, N.Y.)|November 6, 2024
Arab founder variants: Contributions to clinical genomics and precision medicineLama AlAbdi, Sateesh Maddirevula, Bayan Aljamal, et al.
Acta Neuropathologica|December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseasesElena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
Pageof 6