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Ebrahim Sakhinia

Showing results (1-10 of 89) with videos related to

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Clinical Case Reports|January 30, 2018
Rare 48, XYYY syndrome: case report and review of the literatureMaryam Abedi, Arash Salmaninejad, Ebrahim Sakhinia
Laboratory Medicine|November 29, 2017
Pharmacogenetics-Based Warfarin Dosing in Patients With Cardiac Valve Replacement: The Effects of CYP2C9 and VKORC1 Gene PolymorphismsNegin Farzamikia, Ebrahim Sakhinia, Abbas Afrasiabirad
Iranian Journal of Pediatrics|December 24, 2014
Holoprosencephaly and klinefelter syndromeShahin Abdollahifakhim, Ebrahim Sakhinia, Mehrnoosh Mousaviagdas
Laboratory Medicine|May 4, 2019
MicroRNA-221 and MicroRNA-222 in Common Human Cancers: Expression, Function, and Triggering of Tumor Progression as a Key ModulatorSima Amini, Atefe Abak, Ebrahim Sakhinia, et al.
EXCLI Journal|May 11, 2018
Microsatellite instability in colorectal cancerJafar Nouri Nojadeh, Shahin Behrouz Sharif, Ebrahim Sakhinia
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 24, 2004
PolyA PCR amplification of cDNA from RNA extracted from formalin-fixed paraffin-embedded tissueRichard Byers, Jamie Roebuck, Ebrahim Sakhinia, et al.
Hematology/Oncology and Stem Cell Therapy|October 30, 2016
A novel TNFRSF1A gene mutation in a patient with tumor necrosis factor receptor-associated periodic syndromeAlireza Khabazi, Mahafarin Maralani, Sasan Andalib, et al.
Hematology (Amsterdam, Netherlands)|July 18, 2015
Evaluation of IGK and IGL molecular gene rearrangements according to the BIOMED-2 protocols for clinical diagnosis of Hodgkin lymphomaSaeid Ghorbian, Issa Jahanzad, Gholam Reza Javadi, et al.
Cancer Genetics|October 26, 2022
Partial tandem duplication of KMT2A gene in patient afflicted with hypereosinophilic syndrome: A case reportFaramarz Ghasemian Sorbeni, Atefeh Ansarin, Ebrahim Sakhinia, et al.
Gene|January 1, 2018
Variants in GNPTAB, GNPTG and NAGPA genes are associated with stutterersNima Kazemi, Mehrdad Asghari Estiar, Hassan Fazilaty, et al.
Pageof 9

Showing results (1-10 of 89) with videos related to

Sort By:
Pageof 9
Clinical Case Reports|January 30, 2018
Rare 48, XYYY syndrome: case report and review of the literatureMaryam Abedi, Arash Salmaninejad, Ebrahim Sakhinia
Laboratory Medicine|November 29, 2017
Pharmacogenetics-Based Warfarin Dosing in Patients With Cardiac Valve Replacement: The Effects of CYP2C9 and VKORC1 Gene PolymorphismsNegin Farzamikia, Ebrahim Sakhinia, Abbas Afrasiabirad
Iranian Journal of Pediatrics|December 24, 2014
Holoprosencephaly and klinefelter syndromeShahin Abdollahifakhim, Ebrahim Sakhinia, Mehrnoosh Mousaviagdas
Laboratory Medicine|May 4, 2019
MicroRNA-221 and MicroRNA-222 in Common Human Cancers: Expression, Function, and Triggering of Tumor Progression as a Key ModulatorSima Amini, Atefe Abak, Ebrahim Sakhinia, et al.
EXCLI Journal|May 11, 2018
Microsatellite instability in colorectal cancerJafar Nouri Nojadeh, Shahin Behrouz Sharif, Ebrahim Sakhinia
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 24, 2004
PolyA PCR amplification of cDNA from RNA extracted from formalin-fixed paraffin-embedded tissueRichard Byers, Jamie Roebuck, Ebrahim Sakhinia, et al.
Hematology/Oncology and Stem Cell Therapy|October 30, 2016
A novel TNFRSF1A gene mutation in a patient with tumor necrosis factor receptor-associated periodic syndromeAlireza Khabazi, Mahafarin Maralani, Sasan Andalib, et al.
Hematology (Amsterdam, Netherlands)|July 18, 2015
Evaluation of IGK and IGL molecular gene rearrangements according to the BIOMED-2 protocols for clinical diagnosis of Hodgkin lymphomaSaeid Ghorbian, Issa Jahanzad, Gholam Reza Javadi, et al.
Cancer Genetics|October 26, 2022
Partial tandem duplication of KMT2A gene in patient afflicted with hypereosinophilic syndrome: A case reportFaramarz Ghasemian Sorbeni, Atefeh Ansarin, Ebrahim Sakhinia, et al.
Gene|January 1, 2018
Variants in GNPTAB, GNPTG and NAGPA genes are associated with stutterersNima Kazemi, Mehrdad Asghari Estiar, Hassan Fazilaty, et al.
Pageof 9