Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sana Farooki"'
Autor:
Mohamed Alalem, Mrinalini Bhosale, Atul Ranjan, Satomi Yamamoto, Atsushi Kaida, Shigeto Nishikawa, Alejandro Parrales, Sana Farooki, Shrikant Anant, Subhash Padhye, Tomoo Iwakuma
Publikováno v:
Cancers; Volume 14; Issue 17; Pages: 4187
Accumulation of missense mutant p53 (mutp53) in cancers promotes malignant progression. DNAJA1, a member of HSP40 (also known as J-domain proteins: JDPs), is shown to prevent misfolded or conformational mutp53 from proteasomal degradation. Given freq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::898b66dc2c519c5459f7a575358bf25d
Autor:
Ellen Fraint, Sana Farooki, Elizabeth Klein, Audrey Mauguen, Susan E Prockop, Andromachi Scaradavou, Kevin Curran, Maria Cancio, Barbara Spitzer, Jaap Jan Boelens, Joseph Oved, Andrew Harris, Richard J O'Reilly, Nancy A. Kernan
Publikováno v:
Transplantation and Cellular Therapy. 29:46.e1-46.e6
Poor graft function (PGF) is a life-threatening complication after allogeneic stem cell transplantation (alloSCT). Historically, outcomes of patients with PGF have been very poor, and there are no standardized approaches to treatment. Furthermore, fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dafd30ba0996e405282f7d9e52a2eab3
https://doi.org/10.1016/j.jtct.2022.09.027
https://doi.org/10.1016/j.jtct.2022.09.027
Autor:
Karishma Rao, Melissa Gener, Sana Farooki, Gangaram Akangire, Katherine Chastain, Erin M. Guest
Publikováno v:
Journal of pediatric hematology/oncology. 43(4)
Inflammatory myofibroblastic tumors (IMTs) are rare in neonates. IMTs of the tongue are also very rare in infancy, with only 1 case reported in this age group. The mainstay of therapy has traditionally been surgery, which can be devastating to surrou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d9491bb647473188fb4e3adc352753
https://pubmed.ncbi.nlm.nih.gov/32769570
https://pubmed.ncbi.nlm.nih.gov/32769570
Autor:
Kevin Ginn, Shivarajan Manickavasagam Amudhavalli, Binu Porath, Linda D. Cooley, Sana Farooki, Midhat S. Farooqi, Lauren Grote, Melissa Gener
Publikováno v:
Clinical Genetics. 97:670-671
Medulloblastoma in a Patient with Curry-Jones Syndrome with a mosaic variant, c.1234C > T (p.Leu412Phe), in SMO.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42d02ed065b4c84c0256bc749a568bd1
https://doi.org/10.1111/cge.13681
https://doi.org/10.1111/cge.13681
Autor:
Binu Porath, Lauren Grote, Linda D. Cooley, Kevin Ginn, Melissa Gener, Shivarajan M. Amudhavalli, Midhat S. Farooqi, Sana Farooki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0203f1c58decca66f8decd7b5c201e9
https://doi.org/10.1111/cge.13681/v2/response1
https://doi.org/10.1111/cge.13681/v2/response1
Autor:
Erin M. Guest, Keith J. August, Joy M. Fulbright, Michael J. Burke, Jay M. Portnoy, Lauren Pommert, Sana Farooki, Amanda August
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(1)
Hypersensitivity to pegaspargase is associated with inferior survival in pediatric patients with acute lymphoblastic leukemia and lymphoblastic lymphoma. In the past year, drug-supply shortages have led to the lack of an available alternative to pega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8affa23eb1c33188702e976c5b35310
https://pubmed.ncbi.nlm.nih.gov/31571395
https://pubmed.ncbi.nlm.nih.gov/31571395
Autor:
Oluwaseun Olaiya, Kelstan Ellis, Lisa Tarbell, Nicholas Clark, John Stroh, Sana Farooki, Karen Lewing, Jennifer Linebarger
Publikováno v:
Pediatrics. 147:535-535
Background: Palliative care involvement with pediatric oncology patients improves quality of life and the likelihood of receiving goal-concordant end-of-life care. However, barriers to involvement exist. Between Jan 1, 2017 and Dec 31, 2018, the pedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e6719979e58ebe91252c11c24e668f9
https://doi.org/10.1542/peds.147.3ma6.535a
https://doi.org/10.1542/peds.147.3ma6.535a
Publikováno v:
West Virginia Medical Journal. 2016
Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma. RMS of the ear usually involves the middle ear cavity. Treatment usually involves surgery, multi drug chemotherapy regimen, and high dose external beam radiotherapy (EBRT). We p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::940e6f956539b84a41ca6a0b280c632d
https://doi.org/10.21885/wvmj.2016.20
https://doi.org/10.21885/wvmj.2016.20
Publikováno v:
Blood. 132:5009-5009
BACKGROUND Hemophilia A is an X-linked inherited disorder which affects 1 in 5,000 males and is caused by mutations in the factor VIII (FVIII) gene. Hemophilia is typically diagnosed by measurement of FVIII procoagulant (FVIII:C) activity. Molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78f996ff5e5a5ff07ca9d7589ebaf8ad
https://doi.org/10.1182/blood-2018-99-117614
https://doi.org/10.1182/blood-2018-99-117614