Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Liat Ben-Avi"'
Autor:
Eran Goldin, Yael Goldberg, Ephrat Levy-Lahad, Nitzan Sharon, Tomer Adar, Liat Ben Avi, Rachel Beeri, Colin Pritchard, Hagit N. Baris, Tom Walsh, Mary Claire King, Elizabeth E. Half, Ian Tomlinson, Israela Lerer, Menachem Schechter, Brian H. Shirts, Sari Lieberman, Tamar Peretz
Hereditary mixed polyposis syndrome is a rare colon cancer predisposition syndrome caused by a duplication of a non-coding sequence near the gremlin 1, DAN family BMP antagonist gene (GREM1) originally described in Ashkenazi Jews. Few families with G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3daee138313fef313f29e471fa934350
https://ora.ox.ac.uk/objects/uuid:2c10a178-5823-4f62-8ce8-e2291edd70d0
https://ora.ox.ac.uk/objects/uuid:2c10a178-5823-4f62-8ce8-e2291edd70d0
Autor:
Yael Goldberg, Tamar Peretz, Avital Eilat, Michal Sagi, Tamar Hamburger, Dani Bercovich, Israela Lerer, Liat Ben Avi
Publikováno v:
Familial Cancer. 10:59-63
Founder mutations in BRCA1/2 genes have been detected in several Jewish communities in Israel, including in Ashkenazi Jews and Jews who immigrated to Israel from Iraq, Yemen, Iran and Afghanistan. We analyzed DNA samples of patients of Sephardic orig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::104fe2de10612e2b5b224c7d05e5314a
https://doi.org/10.1007/s10689-010-9395-9
https://doi.org/10.1007/s10689-010-9395-9
Autor:
Nir Sharon, Haim D. Danenberg, Vardiella Meiner, Yechiel Friedlander, Eran Leitersdorf, Liat Ben-Avi, Ronen Durst, Arthur Polak, Chaim Lotan, Yehuda Neumark, Shoshi Spitzen, Ronen Beeri, Gilli Erez
Publikováno v:
Genetic Testing and Molecular Biomarkers. 13:583-587
Macrophage scavenger receptor 1 (MSR1) mediates the uptake of modified low density lipoprotein (LDL)-cholesterol. The significance of MSR1 in atherosclerosis development in animal models is uncertain. In this study we sought to determine the signific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e7f8e429096eec3ec654c56af2a438c
https://doi.org/10.1089/gtmb.2009.0048
https://doi.org/10.1089/gtmb.2009.0048
Autor:
Daliah Galinsky, Chen Shochat, Moran Savion, Yael Goldberg, Dvorah Abeliovich, Revital Kariiv, Dani Bercovich, Tamar Hamburger, Tamar Peretz, Liat Ben-Avi, Rinnat M. Porat, Hana Strul, Eli Pikarsky, Israela Lerer, Ayala Hubert, Inbal Kedar
Publikováno v:
Familial cancer. 9(2)
Mutations in DNA mismatch repair genes underlie lynch syndrome (HNPCC). Lynch syndrome resulting from mutations in MSH6 is considered to be attenuated in comparison to that caused by mutations in MLH1 and MSH2, thus more likely to be under diagnosed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::767e14459d9dbe4d7ce27f19b982d929
https://pubmed.ncbi.nlm.nih.gov/19851887
https://pubmed.ncbi.nlm.nih.gov/19851887
Publikováno v:
Journal of Alzheimer's disease : JAD. 6(5)
Apolipoprotein E (apo E) is an essential constituent of several plasma lipoproteins, and plays an important role in lipoprotein metabolism. The apo E gene exhibits two common functional polymorphisms, producing 3 isoforms known to be associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3688d783fca971ed5e460f2deb55fea5
https://pubmed.ncbi.nlm.nih.gov/15505371
https://pubmed.ncbi.nlm.nih.gov/15505371
Autor:
Ronen, Durst, Deborah, Rund, Daniel, Schurr, Osnat, Eliav, Dina, Ben-Yehuda, Shoshi, Shpizen, Liat, Ben-Avi, Tova, Schaap, Inna, Pelz, Eran, Leitersdorf
Publikováno v:
The Israel Medical Association journal : IMAJ. 4(9)
Low density lipoprotein apheresis is used as a complementary method for treating hypercholesterolemic patients who cannot reach target LDL-cholesterol levels on conventional dietary and drug treatment. The DALI system (direct absorption of lipoprotei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::698d4a87aaef3c8a5423499d8e98899d
https://pubmed.ncbi.nlm.nih.gov/12440228
https://pubmed.ncbi.nlm.nih.gov/12440228
Autor:
Karen, Meir, Daniel, Kitsberg, Irit, Alkalay, Fanny, Szafer, Haim, Rosen, Shoshanna, Shpitzen, Liat Ben, Avi, Bart, Staels, Catherine, Fievet, Vardiella, Meiner, Ingemar, Björkhem, Eran, Leitersdorf
Publikováno v:
The Journal of biological chemistry. 277(37)
CYP27-overexpressed transgenic mice were generated with the use of a human full-length CYP27 coding region cloned into a ubiquitous expression vector. Positive transgenic mice were identified by tail DNA genotyping and high fecal 27-hydroxycholestero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::caa5578c75818ce9ba0a7bf73c52d991
https://pubmed.ncbi.nlm.nih.gov/12119285
https://pubmed.ncbi.nlm.nih.gov/12119285
Autor:
Andreas Busjahn, Simon Heath, Hans-Dieter Faulhaber, Hans Knoblauch, Adam Lowe, Evi Jeschke, Ayeleth Reshef, Heike Baron, Magda Rosenthal, Liat Ben Avi, Bertram Müller-Myhsok, Osnat Eliav, Herbert Schuster, Dror Harats, Astrid Mühl, Sylvia Bähring, Danny Schurr, Friedrich C. Luft, Regina Uhlmann, Shoshi Shpitzen, Atakan Aydin, Eran Leitersdorf, Yechiel Friedlander
Publikováno v:
The American Journal of Human Genetics. (1):157-166
SummaryA cholesterol-lowering gene has been postulated from familial hypercholesterolemia (FH) families having heterozygous persons with normal LDL levels and homozygous individuals with LDL levels similar to those in persons with heterozygous FH. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::546a258c130ea3af02d1ba41d236f174
Autor:
Vardiella Meiner, Maritha J. Kotze, Yechiel Friedlander, Roberto Colombo, Shoshi Shpitzen, Joep C. Defesche, Liat Ben Avi, Frederick J. Raal, Eran Leitersdorf, Roni Wexler, Michail Y. Mandelshtam, David Marais, Ronen Durst
Publikováno v:
American journal of human genetics, 68(5), 1172-1188. Cell Press
G197del is the most prevalent LDL receptor (LDLR) mutation causing familial hypercholesterolemia (FH) in Ashkenazi Jew (AJ) individuals. The purpose of this study was to determine the origin, age, and population distribution of G197del, as well as to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2061212fe5456c16ccf80078e81d342f