Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nathaly Marcoux"'
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:
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:
Sharon Noy-Lotan, Orly Dgany, Roxane Lahmi, Nathaly Marcoux, Tanya Krasnov, Nissan Yissachar, Doron Ginsberg, Benny Motro, Peretz Resnitzky, Isaac Yaniv, Gary M. Kupfer, Hannah Tamary
Publikováno v:
Haematologica, Vol 94, Iss 5 (2009)
Background Congenital dyserythropoietic anemia type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. Distinct erythroid precursors with internuclear c
Externí odkaz:
https://doaj.org/article/53d77ab182cb4ac887fb5899e36c705e
Autor:
Nathaly Marcoux, Simon Cloutier, Ewa Zakrzewska, Yves Bourbonnais, Dominick Pallotta, Pierre-Mathieu Charest
Publikováno v:
Scopus-Elsevier
Profilin plays an important role in actin organization in all eukaryotic cells through mechanisms that are still poorly understood. We had previously shown that Mid2p, a transmembrane protein and a potential cell wall sensor, is an effective multicop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fd9ecc050f5a13c0a7e00875c79f99f
https://doi.org/10.1093/genetics/156.2.579
https://doi.org/10.1093/genetics/156.2.579
Publikováno v:
Protoplasma. 210:45-51
Profilin is a ubiquitous actin-monomer-binding protein. The protistPhysarum polycephalum contains two profilins, ProA and ProP, present in amoebae and plasmodia, respectively. We have used mutantSaccharomyces cerevisiae cells in an attempt to observe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2407b70520923e800bcb4226c6ae046
https://doi.org/10.1007/bf01314954
https://doi.org/10.1007/bf01314954
Publikováno v:
Molecular Microbiology. 29:515-526
Profilin-deficient Saccharomyces cerevisiae cells show abnormal growth, actin localization, chitin deposition, bud formation and cytokinesis. Previous studies have also revealed a synthetic lethality between pfy1 and late secretory mutants, suggestin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58abdb03e66bdbe96b434bc9524be716
https://doi.org/10.1046/j.1365-2958.1998.00944.x
https://doi.org/10.1046/j.1365-2958.1998.00944.x
Autor:
Orly Dgany, Isaac Yaniv, Benny Motro, Nissan Yissachar, Hannah Tamary, Nathaly Marcoux, Doron Ginsberg, Sharon Noy-Lotan, Gary M. Kupfer, Tanya Krasnov, Roxane Lahmi, Peretz Resnitzky
Background Congenital dyserythropoietic anemia type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. Distinct erythroid precursors with internuclear c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6857f3445a603c99d491b44a35748294
https://europepmc.org/articles/PMC2675674/
https://europepmc.org/articles/PMC2675674/
Autor:
Kristiina Vuori, Nathaly Marcoux
Publikováno v:
Oncogene. 22(38)
Organization of the actin cytoskeleton in eucaryotic cells is controlled by small GTPases of the Rho family. Rac becomes activated by growth factor stimulation and integrin-mediated cell adhesion to extracellular matrix and is known to have a crucial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc2cf401ba8d673fb43bdd5eeff726ad
https://pubmed.ncbi.nlm.nih.gov/12955089
https://pubmed.ncbi.nlm.nih.gov/12955089
Publikováno v:
Blood. 116:1004-1004
Abstract 1004 Congenital dyserythropoietic anemia type I (CDA1) is an inherited recessive macrocytic anemia associated with ineffective erythropoiesis. The disorder is characterized by the accumulation of erythroid precursors containing spongy hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ee8a649836f7a46f11ba3b84a6b196c
https://doi.org/10.1182/blood.v116.21.1004.1004
https://doi.org/10.1182/blood.v116.21.1004.1004
Autor:
Orly Dgany, Nathaly Marcoux, Sharon Noy-Lotan, Doron Ginsberg, Benny Motro, Nissan Yissachar, Isaac Yaniv, Hannah Tamary, Gary M. Kupfer, Tanya Krasnov, Peretz Resnitzky, Roxane Lahmi
Publikováno v:
Blood. 112:483-483
Congenital dyserythropoietic anemia (CDA) type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. Distinct erythroid precursors with inter-nuclear chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::035d6c677675e428870100909dcdf758
https://doi.org/10.1182/blood.v112.11.483.483
https://doi.org/10.1182/blood.v112.11.483.483