Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sivan Koka"'
Autor:
Sari Lieberman, Ariela Tomer, Avi Ben-Chetrit, Oded Olsha, Shalom Strano, Rachel Beeri, Sivan Koka, Hila Fridman, Karen Djemal, Itzhak Glick, Todd Zalut, Shlomo Segev, Miri Sklair, Bella Kaufman, Amnon Lahad, Aviad Raz, Ephrat Levy-Lahad
Publikováno v:
Genetics in Medicine. 19:754-762
Population screening of three common BRCA1/BRCA2 mutations in Ashkenazi Jews (AJ) apparently fulfills screening criteria. We compared streamlined BRCA screening via self-referral with proactive recruitment in medical settings.Unaffected AJ, age ≥25
Autor:
Sari Lieberman, Bella Kaufman, Aviad E. Raz, Ephrat Levy-Lahad, Itzhak Glick, Oded Olsha, Avi Ben-Chetrit, Karen Djemal, Miri Sklair, Ariela Tomer, Sivan Koka, Todd Zalut, Rachel Beeri, Shalom Strano, Hila Fridman, Shlomo Segev, Amnon Lahad
Publikováno v:
Genetics in Medicine. 22:672
Population screening of three common BRCA1/BRCA2 mutations in Ashkenazi Jews (AJ) apparently fulfills screening criteria. We compared streamlined BRCA screening via self-referral with proactive recruitment in medical settings. Unaffected AJ, age ≥2
Familial communication and cascade testing among relatives of BRCA population screening participants
Autor:
Aviad E. Raz, Malka BenUziyahu, Ariela Tomer, Amnon Lahad, Sivan Koka, Sari Lieberman, Ephrat Levy-Lahad
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 20(11)
Population BRCA1/BRCA2 screening identifies carriers irrespective of family history, yet this information is actionable for relatives. We examined familial communication rates and cascade testing in the screening setting and assessed sociodemographic
Autor:
Graciela Spivak, Reut Erel-Segal, Limor Kalfon, Zvi Segal, Sivan Koka, Bella Gross, Shlomi Orgal, Zohar Keren, Ora Bitterman-Deutsch, Sara Chaim, Yishay Shoval, Hanoch Slor, Tzipora C Falik-Zaccai, Liran Horev, Philip C. Hanawalt
Publikováno v:
Environmental and Molecular Mutagenesis. 53:505-514
The XPD protein plays a pivotal role in basal transcription and in nucleotide excision repair (NER) as one of the ten known components of the transcription factor TFIIH. Mutations in XPD can result in the DNA repair-deficient diseases xeroderma pigme