Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alvin P. Jogasuria"'
Autor:
Julianne N.P. Smith, Dawn M. Dawson, Kelsey F. Christo, Alvin P. Jogasuria, Mark J. Cameron, Monika I. Antczak, Joseph M. Ready, Stanton L. Gerson, Sanford D. Markowitz, Amar B. Desai
Publikováno v:
JCI Insight, Vol 6, Iss 6 (2021)
The splenic microenvironment regulates hematopoietic stem and progenitor cell (HSPC) function, particularly during demand-adapted hematopoiesis; however, practical strategies to enhance splenic support of transplanted HSPCs have proved elusive. We ha
Externí odkaz:
https://doaj.org/article/6ee60674db1947ed9c4037c1257d9dd7
Autor:
Kelsey F. Christo, Sanford D. Markowitz, Alvin P. Jogasuria, Amar Desai, Folashade Otegbeye, Joseph M. Ready, Stanton L. Gerson, Julianne N.P. Smith, Monika I. Antczak
Publikováno v:
Biol Blood Marrow Transplant
Aplastic anemia (AA) is a human immune-mediated bone marrow failure syndrome that is treated by stem cell transplantation for patients who have a matched related donor and by immunosuppressive therapy (IST) for those who do not. Responses to IST are
Autor:
Lakshmi Kasturi, Yongyou Zhang, Julianne N.P. Smith, Young Soo Park, Won Jin Ho, Matthew Hadiono, Kelsey F. Christo, Amar Desai, Alvin P. Jogasuria, Sanford D. Markowitz, Dawn M. Dawson, Stanton L. Gerson, Alyssia V. Broncano
Emerging evidence implicates the eicosanoid molecule prostaglandin E2 (PGE2) in conferring a regenerative phenotype to multiple organ systems following tissue injury. As aging is in part characterized by loss of tissue stem cells’ regenerative capa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a423772524a11b5201e77aef12572a3a
https://doi.org/10.1101/2020.12.22.424017
https://doi.org/10.1101/2020.12.22.424017
Autor:
Sanford D. Markowitz, Dawn M. Dawson, Julianne N.P. Smith, Kelsey F. Christo, Amar Desai, Joseph M. Ready, Stanton L. Gerson, Alvin P. Jogasuria, Monika I. Antczak, Mark J. Cameron
Publikováno v:
JCI Insight
JCI Insight, Vol 6, Iss 6 (2021)
JCI Insight, Vol 6, Iss 6 (2021)
The splenic microenvironment regulates hematopoietic stem and progenitor cell (HSPC) function, particularly during demand-adapted hematopoiesis, however practical strategies to enhance splenic support of transplanted HSPCs have proven elusive. We hav
Autor:
Julianne N.P. Smith, Alvin P. Jogasuria, Matthew D Witkin, Thomas M. Raffay, Kelsey F. Christo, Sanford D. Markowitz, Amar Desai
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterized by interstitial remodeling and pulmonary dysfunction. The etiology of IPF is not completely understood but involves pathologic inflammation and subsequent failure to resolve f
Autor:
Folashade Otegbeye, Kelsey F. Christo, Alvin P. Jogasuria, Amar Desai, Sanford D. Markowitz, Stanton L. Gerson, Julianne N.P. Smith
Aplastic anemia (AA) is a human immune mediated bone-marrow failure syndrome that is treated by stem cell transplantation for patients who have a matched related donor or immunosuppressive therapy (IST) for those who do not. Responses to IST are vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b394c5bdcd56d66017b3f73179c178ae
https://doi.org/10.1101/2020.04.07.030312
https://doi.org/10.1101/2020.04.07.030312
Autor:
Thomas M. Raffay, Alvin P. Jogasuria, Julianne N.P. Smith, Witkin, Sanford D. Markowitz, Kelsey F. Christo, Amar Desai
Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterized by interstitial remodeling and pulmonary dysfunction. The etiology of IPF is not completely understood but involves pathologic inflammation and subsequent failure to resolve f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9728a31e02be7d5aff1a88f6229723b4
https://doi.org/10.1101/2019.12.16.878215
https://doi.org/10.1101/2019.12.16.878215
Autor:
Julianne N.P. Smith, Folashade Otegbeye, Alvin P. Jogasuria, Amar Desai, Sanford D. Markowitz
Publikováno v:
Blood. 134:1220-1220
Acquired aplastic anemia (AA) is a primary bone marrow (BM) failure syndrome in which hematopoietic stem cells (HSC) are depleted in an immune-mediated fashion. AA is rare, with an estimated 900 new cases per year in the U.S., and onset is typically