Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Whitney S. Thompson"'
1
Akademický článek
Risk reduction for small cell cancer of the ovary, hypercalcemic type in prepubertal patient: A clinical and bioethical perspective
Autor: John A. Vu, Whitney S. Thompson, Denise B. Klinkner, Asma Chattha, Myra Wick, Ellen J. Case, Christopher Collura, Amanika Kumar
Publikováno v: Gynecologic Oncology Reports, Vol 49, Iss , Pp 101261- (2023)
Loss of heterozygosity in the SMARCA4 gene is a hallmark feature of small cell carcinoma of the ovary, hypercalcemic type (SCCOHT), an aggressive ovarian cancer occurring in young adults and adolescents with an average age of 23 years and a median su
Externí odkaz: https://doaj.org/article/89d3e62dadfb4c018b8f32a0a14d8356
Zobrazit plný text záznamu
2
Neonatal Diagnosis of Alveolar Capillary Dysplasia via Rapid Genomic Sequencing: A New Gold Standard?
Autor: Whitney S. Thompson, Ellen M. Bendel-Stenzel, Brendan C. Lanpher, Grace M. Arteaga, Raymond C. Stetson, Stephanie C. Mavis
Publikováno v: Neonatology. :1-5
Classic alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a rare congenital lung disorder presenting in the early neonatal period with refractory hypoxemic respiratory failure and pulmonary hypertension. No curative treatm
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f39c301f76af39d0582cc5f622b9614f
https://doi.org/10.1159/000529439
Zobrazit plný text záznamu
7
The future of gene-targeted therapy for hereditary tyrosinemia type 1 as a lead indication among the inborn errors of metabolism
Autor: Robert A. Kaiser, Joseph B. Lillegard, Caitlin J. VanLith, Gourish Mondal, Whitney S. Thompson
Publikováno v: Expert opinion on orphan drugs
Introduction: Inborn errors of metabolism (IEMs) often result from single-gene mutations and collectively cause liver dysfunction in neonates leading to chronic liver and systemic disease. Current treatments for many IEMs are limited to maintenance t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::653ea72a552753774304906e5a6a1272
https://pubmed.ncbi.nlm.nih.gov/33224636
Zobrazit plný text záznamu
8
Cells with Treg-specific FOXP3 demethylation but low CD25 are prevalent in autoimmunity
Autor: Xin Yang, Xaquin Castro Dopico, Henry Z. Simons, Whitney S. Thompson, Linda S. Wicker, Natalia Savinykh, Antony J. Cutler, João J. Oliveira, Ricardo C. Ferreira, Helen Baxendale, Deborah J. Smyth, David B. Dunger, Meghavi Mashar, John A. Todd, Timothy J. Vyse, Marcin L. Pekalski, Chris Wallace, Daniel B. Rainbow, Anita Chandra
Publikováno v: Ferreira, R C, Simons, H Z, Thompson, W S, Rainbow, D B, Yang, X, Cutler, A J, Oliveira, J, Castro Dopico, X, Smyth, D J, Savinykh, N, Mashar, M, Vyse, T J, Dunger, D B, Baxendale, H, Chandra, A, Wallace, C, Todd, J A, Wicker, L S & Pekalski, M L 2017, ' Cells with Treg-specific FOXP3 demethylation but low CD25 are prevalent in autoimmunity ', Journal of Autoimmunity . https://doi.org/10.1016/j.jaut.2017.07.009
Journal of Autoimmunity
Identification of alterations in the cellular composition of the human immune system is key to understanding the autoimmune process. Recently, a subset of FOXP3+ cells with low CD25 expression was found to be increased in peripheral blood from system
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adac702b206c46f970d488f2044c11f8
http://ora.ox.ac.uk/objects/uuid:
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje