Adam Underwood
Overview
Explore the profile of Adam Underwood including associated specialties, affiliations and a list of published articles.
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12
Citations
140
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0
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Recent Articles
1.
Prokop J, Alberta S, Witteveen-Lane M, Pell S, Farag H, Bhargava D, et al.
Microorganisms
. 2024 Sep;
12(9).
PMID: 39338537
As of 2024, SARS-CoV-2 continues to propagate and drift as an endemic virus, impacting healthcare for years. The largest sequencing initiative for any species was initiated to combat the virus,...
2.
Del Puerto H, Miranda A, Qutob D, Ferreira E, Silva F, Lima B, et al.
Genes (Basel)
. 2024 Jun;
15(6).
PMID: 38927713
Members of the SOX (SRY-related HMG box) family of transcription factors are crucial for embryonic development and cell fate determination. This review investigates the role of SOX3 in cancer, as...
3.
Underwood A, Rasicci D, Hinds D, Mitchell J, Zieba J, Mills J, et al.
Genes (Basel)
. 2023 Jan;
14(1).
PMID: 36672963
The SOX transcription factor family is pivotal in controlling aspects of development. To identify genotype-phenotype relationships of SOX proteins, we performed a non-biased study of SOX using 1890 open-reading frame...
4.
de Souza Silva F, Underwood A, Almeida C, Ribeiro T, Souza-Fagundes E, Martins A, et al.
Med Oncol
. 2022 Sep;
39(12):212.
PMID: 36175695
Background: Sex-determining region Y-box 3 (SOX3) protein, a SOX transcriptions factors group, has been identified as a key regulator in several diseases, including cancer. Downregulation of transcriptions factors in invasive...
5.
Nascimento D, Balaniuc S, Palhares D, Underwood A, Palhares M, Alves F, et al.
Intractable Rare Dis Res
. 2021 Sep;
10(3):179-189.
PMID: 34466340
Fibrodysplasia Ossificans Progressiva (FOP) is a rare congenital intractable disease associated with a mutation in gene, characterized by skeleton malformations. Ascorbic acid (AA) and propranolol (PP) in combination is reported...
6.
Afrin A, Prokop J, Underwood A, Uhl K, VanSickle E, Baruwal R, et al.
Cold Spring Harb Mol Case Stud
. 2020 Dec;
6(6).
PMID: 33335012
We present a male patient born at 38-wk gestation with rhizomelic shortening of extremities, hepatomegaly, ventriculomegaly, heart failure, severely depressed left ventricular function, biventricular hypertrophy, and biatrial enlargement. Additional physical...
7.
Sirpilla O, Bauss J, Gupta R, Underwood A, Qutob D, Freeland T, et al.
J Proteome Res
. 2020 Jul;
19(11):4275-4290.
PMID: 32686937
SARS-CoV-2 (COVID-19) has infected millions of people worldwide, with lethality in hundreds of thousands. The rapid publication of information, both regarding the clinical course and the viral biology, has yielded...
8.
Gupta R, Charron J, Stenger C, Painter J, Steward H, Cook T, et al.
J Biol Chem
. 2020 Jun;
295(33):11742-11753.
PMID: 32587094
The pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has challenged the speed at which laboratories can discover the viral composition and study health outcomes. The small ∼30-kb...
9.
Gupta R, Charron J, Stenger C, Painter J, Steward H, Cook T, et al.
bioRxiv
. 2020 Jun;
PMID: 32511397
The SARS-CoV-2 pandemic, starting in 2019, has challenged the speed at which labs perform science, ranging from discoveries of the viral composition to handling health outcomes in humans. The small...
10.
Palhares D, Nascimento D, Palhares M, Lopes S, de L, Cristhina P, et al.
Intractable Rare Dis Res
. 2019 Mar;
8(1):24-28.
PMID: 30881854
Fibrodysplasia ossificans progressiva (FOP) is a rare, intractable and devastating genetic connective tissue disorder characterized by progressive ectopic ossification in the soft tissues and skeleton. Three patients, one teenage girl...