Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Manisha Gadgeel"'
Publikováno v:
Cells, Vol 13, Iss 11, p 963 (2024)
Primary Epstein–Barr virus (EBV) infection which can manifest as infectious mononucleosis (IM) is commonly acquired during childhood. EBV primarily invades B cells leading to a lytic reaction; the control of the infection is handled by natural kill
Externí odkaz:
https://doaj.org/article/6cf30065bfbb4642af60d3173fa2b65e
Publikováno v:
Haematologica, Vol 107, Iss 11 (2022)
Externí odkaz:
https://doaj.org/article/88f5a64a1a784493be8ebf8f84be988e
Autor:
Ahmar Urooj Zaidi, Steven Buck, Manisha Gadgeel, Miguel Herrera-Martinez, Araathi Mohan, Kenya Johnson, Shruti Bagla, Robert M. Johnson, Yaddanapudi Ravindranath
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
The measurement of band 3 (AE1, SLC4A1, CD233) content of red cells by eosin-5- maleimide (EMA) staining is swiftly replacing conventional osmotic fragility (OF) test as a tool for laboratory confirmation of hereditary spherocytosis across the globe.
Externí odkaz:
https://doaj.org/article/bdac5d7b497d4c2b84330df110beb8d8
Autor:
Shruti Bagla, Kanta Bhambhani, Manisha Gadgeel, Steven Buck, Jian-Ping Jin, Yaddanapudi Ravindranath
Publikováno v:
Haematologica, Vol 104, Iss 9 (2019)
Externí odkaz:
https://doaj.org/article/998d791c3e134ea5b36faa0ebfd19ce8
Publikováno v:
Leukemia & Lymphoma. 63:1331-1338
The interactions between Hodgkin and Reed Sternberg cells and tumor microenvironment, the changes that occur with therapy and, in particular, checkpoint inhibition are not fully understood. Understanding these is key to optimizing outcomes for patien
Autor:
Jeffrey W. Taub, Batool Al‐Qanber, Süreyya Savaşan, Yaddanapudi Ravindranath, Steven Buck, Manisha Gadgeel
Publikováno v:
Annals of Hematology. 100:1695-1700
Children with Down syndrome (DS) are at an increased risk of developing transient abnormal myelopoiesis (TAM) and acute leukemia. Aberrant expression of CD56 has been observed on myeloid leukemic blasts in DS patients. In general, CD56 expression in
Autor:
Ahmar U. Zaidi, Steven Buck, Michael Chicka, Katherine Regling, Yaddanapudi Ravindranath, Meera Chitlur, Shruti Bagla, Leigh Anne Flore, Erin Wakeling, Manisha Gadgeel, Charles A. Schiffer
Publikováno v:
Pediatric Hematology and Oncology. 38:65-79
RUNX1 associated familial platelet disorder (FPD) is a rare autosomal dominant hematologic disorder characterized by thrombocytopenia and/or altered platelet function. There is an increased propensity to develop myeloid malignancy (MM) - acute myeloi
Publikováno v:
Annals of Hematology. 100:2661-2663
Publikováno v:
Journal of Clinical Pathology. 73:176-179
AimsTo compare immunological microenvironments in local and distant lymphoid tissues in Hodgkin’s lymphoma (HL) in children.MethodsWe have analysed diagnostic bone marrow (BM) samples in 22 and corresponding involved lymph node (LN) in eight and pe
Autor:
Tristan Knight, Manisha Gadgeel, Shengnan Wu, Yaddanapudi Ravindranath, Ahmar U. Zaidi, Steven Buck
Publikováno v:
Pediatric Hematology and Oncology. 36:317-326
Piezo1, encoded by the gene PIEZO1, is an erythrocytic cellular membrane mechanoactivated cation channel. Mutations have been implicated in erythrocyte volume disorders (EVDs)—especially hereditary...