Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Sharon Noy Lotan"'
Autor:
Orna Steinberg-Shemer, Naama Orenstein, Tanya Krasnov, Sharon Noy-Lotan, Nathaly Marcoux, Orly Dgany, Joanne Yacobovich, Oded Gilad, Evelyn Shabad, Lina Basel-Salmon, Hannah Tamary
Publikováno v:
Platelets, Vol 33, Iss 4, Pp 645-648 (2022)
The transcription factor MEIS1 (myeloid ectotrophic insertion site 1) is crucial for the maintenance of hematopoietic stem cells and for megakaryopoiesis. Germline variants in MEIS1 are associated with restless-leg syndrome, but were not previously s
Externí odkaz:
https://doaj.org/article/a0653529476b4a479f065e4aeeccb2e1
Autor:
Oded Gilad, Orly Dgany, Sharon Noy-Lotan, Tanya Krasnov, Joanne Yacobovich, Ron Rabinowicz, Tracie Goldberg, Amir A. Kuperman, Abed Abu-Quider, Hagit Miskin, Noa Kapelushnik, Noa Mandel-Shorer, Shai Shimony, Dan Harlev, Tal Ben-Ami, Etai Adam, Carina Levin, Shraga Aviner, Ronit Elhasid, Sivan Berger-Achituv, Lilach Chaitman-Yerushalmi, Yona Kodman, Nino Oniashvilli, Michal Hameiri-Grosman, Shai Izraeli, Hannah Tamary, Orna Steinberg-Shemer
Publikováno v:
Haematologica, Vol 107, Iss 9 (2022)
Prolonged cytopenias are a non-specific sign with a wide differential diagnosis. Among inherited disorders, cytopenias predisposing to leukemia require a timely and accurate diagnosis to ensure appropriate medical management, including adequate monit
Externí odkaz:
https://doaj.org/article/2af097b8e32e424dbac3cc84f018611c
Autor:
Grace Swickley, Yehoshua Bloch, Lidor Malka, Adi Meiri, Sharon Noy-Lotan, Amiel Yanai, Hannah Tamary, Benny Motro
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which erythroid precursors in the bone marrow exhibit pathognomonic abnormalities including spongy heterochromatin and
Externí odkaz:
https://doaj.org/article/6e117771ef5c441294be37568e85ff4e
Autor:
Sharon Noy-Lotan, Orly Dgany, Nathaly Marcoux, Ayelet Atkins, Gary M. Kupfer, Linette Bosques, Christine Gottschalk, Orna Steinberg-Shemer, Benny Motro, Hannah Tamary
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Congenital dyserythropoietic anemia type I (CDA I) is an autosomal recessive disease characterized by moderate to severe macrocytic anemia and pathognomonic morphologic abnormalities of the erythroid precursors, including spongy heterochromatin. The
Externí odkaz:
https://doaj.org/article/de2db599c3204c6095f47339336c7633
Autor:
Orna Steinberg-Shemer, Tracie A. Goldberg, Joanne Yacobovich, Carina Levin, Ariel Koren, Shoshana Revel-Vilk, Tal Ben-Ami, Amir A. Kuperman, Vered Shkalim Zemer, Amos Toren, Joseph Kapelushnik, Ayelet Ben-Barak, Hagit Miskin, Tanya Krasnov, Sharon Noy-Lotan, Orly Dgany, Hannah Tamary
Publikováno v:
Haematologica, Vol 105, Iss 7 (2020)
Fanconi anemia (FA), an inherited bone marrow failure (BMF) syndrome, caused by mutations in DNA repair genes, is characterized by congenital anomalies, aplastic anemia, high risk of malignancies and extreme sensitivity to alkylating agents. We aimed
Externí odkaz:
https://doaj.org/article/b3c169549a8b461cb724899e84217133
Autor:
Benny Motro, Lidor Malka, Adi Meiri, Yehoshua Bloch, Hannah Tamary, Amiel Yanai, Grace Swickley, Sharon Noy-Lotan
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-12 (2020)
BMC Molecular and Cell Biology
BMC Molecular and Cell Biology
Background Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which erythroid precursors in the bone marrow exhibit pathognomonic abnormalities including spongy heterochromatin and chromati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b3a34d8112ecd34b06d4148bd206fd0
http://link.springer.com/article/10.1186/s12860-020-00258-1
http://link.springer.com/article/10.1186/s12860-020-00258-1
Autor:
Orna Steinberg-Shemer, Tanya Krasnov, Oded Gilad, Sharon Noy-Lotan, Hannah Tamary, Orly Dgany, Joanne Yacobovich
Publikováno v:
Acta Haematologica. 143:432-437
Background/Objective: Alpha-thalassemia is one of the most prevalent genetic diseases, with the –α3.7 deletion being the most common mutation. Molecular studies have suggested mechanisms to explain the mild phenotype of “silent carrier” hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f2a3bc58454ab3153f09578974e406
https://doi.org/10.1159/000503023
https://doi.org/10.1159/000503023
Autor:
Oded Gilad, Orly Dgany, Sharon Noy-Lotan, Tanya Krasnov, Joanne Yacobovich, Ron Rabinowicz, Tracie Goldberg, Amir A. Kuperman, Abed Abu-Quider, Hagit Miskin, Noa Kapelushnik, Noa Mandel-Shorer, Shai Shimony, Dan Harlev, Tal Ben-Ami, Etai Adam, Carina Levin, Shraga Aviner, Ronit Elhasid, Sivan Berger-Achituv, Lilach Chaitman-Yerushalmi, Yona Kodman, Nino Oniashvilli, Michal Hameiri-Grosman, Shai Izraeli, Hannah Tamary, Orna Steinberg-Shemer
Publikováno v:
Haematologica. 107(9)
Prolonged cytopenias are a non-specific sign with a wide differential diagnosis. Among inherited disorders, cytopenias predisposing to leukemia require a timely and accurate diagnosis to ensure appropriate medical management, including adequate monit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a8b7befaa189011fac46dd0a3c5731
https://pubmed.ncbi.nlm.nih.gov/35295078
https://pubmed.ncbi.nlm.nih.gov/35295078
Autor:
Amir A. Kuperman, Tracie A. Goldberg, Carina Levin, Hannah Tamary, Orly Dgany, Tanya Krasnov, Orna Steinberg-Shemer, Joseph Kapelushnik, Hagit Miskin, Vered Shkalim Zemer, Ariel Koren, Ayelet Ben-Barak, Tal Ben-Ami, Sharon Noy-Lotan, Joanne Yacobovich, Shoshana Revel-Vilk, Amos Toren
Publikováno v:
Haematologica
Fanconi anemia (FA), an inherited bone marrow failure (BMF) syndrome, caused by mutations in DNA repair genes, is characterized by congenital anomalies, aplastic anemia, high risk of malignancies and extreme sensitivity to alkylating agents. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96a3f37a4c55fac889e18c424d8d6aef
https://doi.org/10.3324/haematol.2019.222877
https://doi.org/10.3324/haematol.2019.222877
Autor:
Jerry Stein, Shlomit Barzilai Birenboim, Ifat Geron, Asaf D Yanir, Hila Fishman, Orna Steinberg-Shemer, Galia Avrahami, Yona Kodman, Sharon Noy Lotan, Jacques Mardoukh, Tatyana Krasnov, Yehudit Birger, Aviva Krauss, Shai Izraeli, Tamar Feuerstein, Joanne Yacobovich, Hannah Tamary, Orly Dgany, Oded Gilad
Publikováno v:
Pediatric bloodcancerREFERENCES. 68(10)
BACKGROUND Inflammatory manifestations (IM) are well described in adult patients with myelodysplastic syndrome (MDS), but the presentation is highly variable and no standardized treatment exists. This phenomenon is rarely reported in children. As mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6b75be265579250adcf5d7c74f42ac
https://pubmed.ncbi.nlm.nih.gov/34019335
https://pubmed.ncbi.nlm.nih.gov/34019335