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Autor:
Shiran Bar, Dan Vershkov, Gal Keshet, Elyad Lezmi, Naama Meller, Atilgan Yilmaz, Ofra Yanuka, Malka Nissim-Rafinia, Eran Meshorer, Talia Eldar-Geva, Nissim Benvenisty
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
Genetic imprinting ensures monoallelic gene expression critical for normal embryonic development. Here the authors take advantage of human haploid parthenogenic embryonic stem cells lacking paternal alleles to identify, by genome-wide screening, fact
Externí odkaz:
https://doaj.org/article/207e85234f0e4fce91d514642b759697
Publikováno v:
Stem Cell Reports. 18:817-828
Autor:
Jennia Michaeli, Riham Smoom, Noa Serruya, Hosniyah El Ayoubi, Keren Rotshenker-Olshinka, Naama Srebnik, Ofir Michaeli, Talia Eldar-Geva, Yehuda Tzfati
Publikováno v:
Cells, Vol 11, Iss 3, p 513 (2022)
Current social trends of delayed reproduction to the fourth and fifth decade of life call for a better understanding of reproductive aging. Demographic studies correlated late reproduction with general health and longevity. Telomeres, the protective
Externí odkaz:
https://doaj.org/article/eec49e523b264a3685689a4eac819cbc
Publikováno v:
Cell Reports, Vol 19, Iss 5, Pp 957-968 (2017)
Summary: The parent-specific monoallelic expression of imprinted genes is controlled by DNA methylation marks that are established differentially in the germline. Perturbation of these marks leads to loss of imprinting (LOI), which is associated with
Externí odkaz:
https://doaj.org/article/9ef5d5da1af64df0b072642210dae62c
Autor:
Ibrahim Knani, Brian J. Earley, Shiran Udi, Alina Nemirovski, Rivka Hadar, Asaad Gammal, Resat Cinar, Harry J. Hirsch, Yehuda Pollak, Itai Gross, Talia Eldar-Geva, Daniela P. Reyes-Capo, Joan C. Han, Andrea M. Haqq, Varda Gross-Tsur, Rachel Wevrick, Joseph Tam
Publikováno v:
Molecular Metabolism, Vol 5, Iss 12, Pp 1187-1199 (2016)
Objective: Extreme obesity is a core phenotypic feature of Prader–Willi syndrome (PWS). Among numerous metabolic regulators, the endocannabinoid (eCB) system is critically involved in controlling feeding, body weight, and energy metabolism, and a g
Externí odkaz:
https://doaj.org/article/0514992d71c34dd994565af16272ceea
Autor:
Yaara Cohen-Hadad, Gheona Altarescu, Talia Eldar-Geva, Ephrat Levi-Lahad, Ming Zhang, Ekaterina Rogaeva, Marc Gotkine, Osnat Bartok, Reut Ashwal-Fluss, Sebastian Kadener, Silvina Epsztejn-Litman, Rachel Eiges
Publikováno v:
Stem Cell Reports, Vol 7, Iss 5, Pp 927-940 (2016)
We established two human embryonic stem cell (hESC) lines with a GGGGCC expansion in the C9orf72 gene (C9), and compared them with haploidentical and unrelated C9 induced pluripotent stem cells (iPSCs). We found a marked difference in C9 methylation
Externí odkaz:
https://doaj.org/article/9f14e07fd920475989781574b056d061
Publikováno v:
Cell Reports, Vol 27, Iss 1, Pp 20-29.e3 (2019)
Summary: Dosage compensation of sex-chromosome gene expression between male and female mammals is achieved via X chromosome inactivation (XCI) by employing epigenetic modifications to randomly silence one X chromosome during early embryogenesis. Huma
Externí odkaz:
https://doaj.org/article/867655b9223647f8a1749369769f0e9c
Autor:
Hananel Holzer, A. Weintruab, Michael Gal, Oshrat Schonberger, Talya Miron-Shatz, Avi Tsafrir, Naama Srebnik, D. Goldberg, J. Hyman, I. Ben Ami, Talia Eldar-Geva, N. Dekel
Publikováno v:
Reproductive BioMedicine Online. 43:1137-1145
Research question What are the reproductive choices and retrospective reflections of women at least 4 years after planned oocyte cryopreservation (POC)? Design This was an internet survey, using the REDCap application, of women who underwent POC, at
Autor:
Pauline Megalli, Talia Eldar-Geva, Rachel Eiges, Silvina Epsztejn-Litman, Gheona Altarescu, Oshrat Schonberger, Shira Yanovsky-Dagan, Eliora Cohen
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, In press, ⟨10.1038/s41431-021-00999-3⟩
European Journal of Human Genetics, Nature Publishing Group, In press, ⟨10.1038/s41431-021-00999-3⟩
European Journal of Human Genetics, In press, ⟨10.1038/s41431-021-00999-3⟩
European Journal of Human Genetics, Nature Publishing Group, In press, ⟨10.1038/s41431-021-00999-3⟩
Myotonic dystrophy type 1 (DM1) is an autosomal dominant muscular dystrophy that results from a CTG expansion (50–4000 copies) in the 3′ UTR of the DMPK gene. The disease is classified into four or five somewhat overlapping forms, which incomplet