Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Shruti Bagla"'
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, Daniela Cukovic, Eishi Asano, Sandeep Sood, Aimee Luat, Harry T. Chugani, Diane C. Chugani, Alan A. Dombkowski
Publikováno v:
Neurobiology of Disease, Vol 109, Iss , Pp 76-87 (2018)
Tuberous sclerosis complex (TSC) is characterized by hamartomatous lesions in various organs and arises due to mutations in the TSC1 or TSC2 genes. TSC mutations lead to a range of neurological manifestations including epilepsy, cognitive impairment,
Externí odkaz:
https://doaj.org/article/94db65309d3c464e81b9a9b243d13543
Autor:
Daniela Cukovic, Shruti Bagla, Dylan Ukasik, Paul M. Stemmer, Bhanu P. Jena, Akshata R. Naik, Sandeep Sood, Eishi Asano, Aimee Luat, Diane C. Chugani, Alan A. Dombkowski
Publikováno v:
Non-Coding RNA, Vol 7, Iss 3, p 40 (2021)
Exosomes are a class of small, secreted extracellular vesicles (EV) that have recently gained considerable attention for their role in normal cellular function, disease processes and potential as biomarkers. Exosomes serve as intercellular messengers
Externí odkaz:
https://doaj.org/article/23e20f1469964a0c82388b1a05e4dd68
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:
PLoS ONE, Vol 13, Iss 4, p e0195639 (2018)
Epilepsy is a common neurological disorder, which is not well understood at the molecular level. Exactly why some brain regions produce epileptic discharges and others do not is not known. Patients who fail to respond to antiseizure medication (refra
Externí odkaz:
https://doaj.org/article/cdb1ba50efc94342a3802e18dc8039e7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1957c08ca4204299fdfc5df30535355
https://doi.org/10.1080/08880018.2020.1814463
https://doi.org/10.1080/08880018.2020.1814463
Autor:
Manisha Gadgeel, Yaddanapudi Ravindranath, Jian Ping Jin, Steven Buck, Kanta Bhambhani, Shruti Bagla
Publikováno v:
Haematologica. 104:e428-e431
Pyruvate kinase deficiency (PKD) is the most common glycolytic enzyme deficiency causing congenital nonspherocytic hemolytic anemia with a variable clinical severity.[1][1] Approximately 200 mutational variants have been described in the PKLR gene wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9d5f5d388d92090e6173992229bff6f
https://doi.org/10.3324/haematol.2018.214692
https://doi.org/10.3324/haematol.2018.214692
Autor:
Richard Wlodarski, Biswajit Maharathi, Jeffrey A. Loeb, James L. Patton, Jing Hua, Shruti Bagla, Eishi Asano
Publikováno v:
Clin Neurophysiol
Objective Interictal spikes are a biomarker of epilepsy, yet their precise roles are poorly understood. Using long-term neocortical recordings from epileptic patients, we investigated the spatial-temporal propagation patterns of interictal spiking. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4526e8953092c01d55a0cd3116f181e
Autor:
Yogindra Persaud, Shruti Bagla, Yaddanapudi Ravindranath, Christina Shanti, Hamza S Gorsi, Bahig M. Shehata
Publikováno v:
Pediatric Blood & Cancer. 68
Non Rhabdomyosarcoma Soft Tissue Sarcomas (NRSTS) are rare in the pediatric age group, accounting for 1-7% of all pediatric tumors. Leiomyosarcoma, a subtype of NRSTS, is exceedingly rare in pediatric population. Due to the rarity of this condition,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::500e29a1c2576d621e0fbe882296a0c5
https://doi.org/10.1002/pbc.28805
https://doi.org/10.1002/pbc.28805
Autor:
Araathi Mohan, Robert M. Johnson, Shruti Bagla, Manisha Gadgeel, Yaddanapudi Ravindranath, Kenya Johnson, Ahmar U. Zaidi, Steven Buck, Miguel Herrera-Martinez
Publikováno v:
Frontiers in Physiology
Frontiers in Physiology, Vol 11 (2020)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::bffb37ca475bfd765b95847cc8704807