Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Shilpa M. Hattangadi"'
Autor:
Susree Modepalli, Shilpa M. Hattangadi
Publikováno v:
Haematologica, Vol 105, Iss 9 (2020)
Externí odkaz:
https://doaj.org/article/76c802c4c0284507995bb502af8cde5d
Autor:
Amalia Avila Figueroa, James D. Fasano, Sandra Martinez-Morilla, Srividhya Venkatesan, Gary Kupfer, Shilpa M. Hattangadi
Publikováno v:
Haematologica, Vol 103, Iss 8 (2018)
Externí odkaz:
https://doaj.org/article/66f2683d54e64685b5a8fb6154c5e7c6
Autor:
Nathan Brinkman, Andrea Zamperone, Tenzin Choesang, Ronald Hoffman, Christopher E. Mason, Marc Ruiz Martinez, Carla Casu, Matthew MacKay, Mansour Djedaini, Jose Javier Bravo-Cordero, Dechen Lama, Luena Papa, Yelena Ginzburg, Paul Zumbo, Daniel Moskop, Peng Ji, Julie Di Martino, Stefano Rivella, Maria Feola, Shilpa M. Hattangadi, Huiyong Chen, Charles S. Abrams, Antonia Follenzi
Publikováno v:
Communications Biology
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Erythropoiesis involves complex interrelated molecular signals influencing cell survival, differentiation, and enucleation. Diseases associated with ineffective erythropoiesis, such as β-thalassemias, exhibit erythroid expansion and defective enucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9133d58181c41c673c499a42311b7cf
https://doi.org/10.1038/s42003-021-02046-9
https://doi.org/10.1038/s42003-021-02046-9
Autor:
Shilpa M. Hattangadi, Susree Modepalli
Publikováno v:
Haematologica
β-thalassemia major (β-TM) is an inherited hemoglobinopathy caused by a quantitative defect in the synthesis of β-globin chains of hemoglobin, leading to the accumulation of free a-globin chains that aggregate and cause ineffective erythropoiesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5f160f98e0b1ba5186ac70610def34
https://pubmed.ncbi.nlm.nih.gov/33054049
https://pubmed.ncbi.nlm.nih.gov/33054049
Autor:
Shilpa M. Hattangadi, Srividhya Venkatesan, Gary M. Kupfer, Amalia A Figueroa, James D. Fasano, Sandra Martinez-Morilla
Publikováno v:
Haematologica. 103:e341-e344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8afd005ae78558012b8988ad9e8b0840
https://doi.org/10.3324/haematol.2017.171785
https://doi.org/10.3324/haematol.2017.171785
Autor:
Chloe Shaw, Shilpa M. Hattangadi, Gary M. Kupfer, Susree Modepalli, Shangqin Guo, Anna E. Eastman
Publikováno v:
Blood. 136:27-28
Erythropoietic proliferation and differentiation are coordinated and regulated by a complex compendium of molecular components and networks. Understanding the underlying mechanisms and the dependence of erythroid maturation on cell-cycle behavior can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9014ab8b1ab47b0d3e3b456ce8f61485
https://doi.org/10.1182/blood-2020-141666
https://doi.org/10.1182/blood-2020-141666
Autor:
Alexander Koral, Ben Freiberg, Brian Dillon, Raffaella A. Morotti, Pamela L. Valentino, Shilpa M. Hattangadi, Sukru Emre
Publikováno v:
The Journal of pediatrics. 218
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd908ec96d0133197509263940d12c47
https://pubmed.ncbi.nlm.nih.gov/31870607
https://pubmed.ncbi.nlm.nih.gov/31870607
Autor:
Shangqin Guo, Shilpa M. Hattangadi, Chloe Shaw, Susree Modepalli, Anna E. Eastman, Gary Kupfer
Publikováno v:
Experimental Hematology. 88:S32
Aberrant cell cycle speed during hematopoiesis defines pathologic conditions, such as the inability to compensate for anemia in diseases of ineffective erythropoiesis like hemolysis or thalassemia. We utilized a unique live-cell reporter of cell cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dddc0ca19c3bf8028278e6817a25b1e1
https://doi.org/10.1016/j.exphem.2020.09.176
https://doi.org/10.1016/j.exphem.2020.09.176
Publikováno v:
Pediatric Oncology ISBN: 9783319614205
Diamond-Blackfan anemia (DBA) is a rare inherited bone marrow failure syndrome (IBMFS) that presents in early infancy and is characterized by severe anemia with mild macrocytosis, reticulocytopenia, and a normocellular bone marrow with a paucity of e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab1ff058a7c835bb0a2b186b8ec27465
https://doi.org/10.1007/978-3-319-61421-2_7
https://doi.org/10.1007/978-3-319-61421-2_7
Autor:
Anupama Narla, Jeffrey D. Cooney, Nika N. Danial, Carlo Brugnara, Guillaume Vogin, Tamara A. Dailey, Diane M. Ward, Shilpa M. Hattangadi, Barry H. Paw, Slater N. Hurst, Danilo Faccenda, Jessica Wiwczar, Naoko Takahashi-Makise, Caiyong Chen, Dean R. Campagna, Yi Zhou, Amy E. Medlock, Jerry Kaplan, Harry A. Dailey, Benjamin L. Ebert, Liangtao Li, Nathaniel B. Langer, Eric L. Pierce, Dhvanit I. Shah, Iman J. Schultz, Michelangelo Campanella, Mark D. Fleming, Spencer K. Heggers, Wen Chen, Alexandra Seguin
Publikováno v:
Nature
Defects in the availability of haem substrates or the catalytic activity of the terminal enzyme in haem biosynthesis, ferrochelatase (Fech), impair haem synthesis and thus cause human congenital anaemias1,2. The interdependent functions of regulators
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c327e500dd919829aba8d52ae2c0e12d
http://europepmc.org/articles/PMC3504625
http://europepmc.org/articles/PMC3504625