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Dalit Ben-Yosef

Showing results (21-30 of 70) with videos related to

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Journal of Assisted Reproduction and Genetics|April 18, 2002
The mitochondrial DNA mutation (deltamtDNA5286) in human oocytes: correlation with age and IVF outcomeVered Yesodi, Yuval Yaron, Joseph B Lessing, et al.
International Journal of Molecular Sciences|August 26, 2022
Transcriptomic Analysis of Human Fragile X Syndrome Neurons Reveals Neurite Outgrowth Modulation by the TGFβ/BMP PathwayLiron Kuznitsov-Yanovsky, Guy Shapira, Lital Gildin, et al.
Reproductive Biomedicine Online|August 29, 2009
First live birth following IVF-embryo transfer and use of GnRHa alone for ovarian stimulationFoad Azem, Beni Almog, Dalit Ben-Yosef, et al.
Prenatal Diagnosis|December 20, 2008
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?Adi Reches, Mira Malcov, Dalit Ben-Yosef, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|December 10, 2022
Cleavage stage at compaction-a good predictor for IVF outcomeRan Matot, Yael Kalma, Roni Rahav, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Clocks and Dominoes: Timing Mechanisms of EmbryogenesisYonghyun Song, Brian D Leahy, Hanspeter Pfister, et al.
Iscience|November 21, 2022
Stabilization of hESCs in two distinct substates along the continuum of pluripotencyChen Dekel, Robert Morey, Jacob Hanna, et al.
Frontiers in Endocrinology|November 12, 2019
The Effect of Advanced Maternal Age on Embryo MorphokineticsMiriam Warshaviak, Yael Kalma, Ariela Carmon, et al.
Fertility and Sterility|December 27, 2008
Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysisMira Malcov, Tsvia Frumkin, Tamar Shwartz, et al.
Cell Reports|September 17, 2013
Genomic analysis of hESC pedigrees identifies de novo mutations and enables determination of the timing and origin of mutational eventsDalit Ben-Yosef, Francesca S Boscolo, Hadar Amir, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Journal of Assisted Reproduction and Genetics|April 18, 2002
The mitochondrial DNA mutation (deltamtDNA5286) in human oocytes: correlation with age and IVF outcomeVered Yesodi, Yuval Yaron, Joseph B Lessing, et al.
International Journal of Molecular Sciences|August 26, 2022
Transcriptomic Analysis of Human Fragile X Syndrome Neurons Reveals Neurite Outgrowth Modulation by the TGFβ/BMP PathwayLiron Kuznitsov-Yanovsky, Guy Shapira, Lital Gildin, et al.
Reproductive Biomedicine Online|August 29, 2009
First live birth following IVF-embryo transfer and use of GnRHa alone for ovarian stimulationFoad Azem, Beni Almog, Dalit Ben-Yosef, et al.
Prenatal Diagnosis|December 20, 2008
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?Adi Reches, Mira Malcov, Dalit Ben-Yosef, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|December 10, 2022
Cleavage stage at compaction-a good predictor for IVF outcomeRan Matot, Yael Kalma, Roni Rahav, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Clocks and Dominoes: Timing Mechanisms of EmbryogenesisYonghyun Song, Brian D Leahy, Hanspeter Pfister, et al.
Iscience|November 21, 2022
Stabilization of hESCs in two distinct substates along the continuum of pluripotencyChen Dekel, Robert Morey, Jacob Hanna, et al.
Frontiers in Endocrinology|November 12, 2019
The Effect of Advanced Maternal Age on Embryo MorphokineticsMiriam Warshaviak, Yael Kalma, Ariela Carmon, et al.
Fertility and Sterility|December 27, 2008
Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysisMira Malcov, Tsvia Frumkin, Tamar Shwartz, et al.
Cell Reports|September 17, 2013
Genomic analysis of hESC pedigrees identifies de novo mutations and enables determination of the timing and origin of mutational eventsDalit Ben-Yosef, Francesca S Boscolo, Hadar Amir, et al.
Pageof 7