Mutations within the putative protease domain of the human FAM111B gene may predict disease severity and poor prognosis: A review of POIKTMP cases

por Arowolo, Afolake, Rhoda, Cenza, Khumalo, Nonhlanhla
Publicado 2022

“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”

por Arowolo, Afolake T., Adeola, Henry A., Khumalo, Nonhlanhla P.
Publicado 2017

Proposed Cellular Function of the Human FAM111B Protein and Dysregulation in Fibrosis and Cancer

por Arowolo, Afolake, Malebana, Moses, Sunda, Falone, Rhoda, Cenza
Publicado 2022

Androgenetic alopecia: An update

por Ntshingila, Sincengile, Oputu, Ogheneochuko, Arowolo, Afolake T., Khumalo, Nonhlanhla P.
Publicado 2023

Apoferritin and Apoferritin-Capped Metal Nanoparticles Inhibit Arginine Kinase of Trypanosoma brucei

por Adeyemi, Oluyomi Stephen, Arowolo, Afolake T., Hetta, Helal F., Al-Rejaie, Salim, Rotimi, Damilare, Batiha, Gaber El-Saber
Publicado 2020

Hypoxia and the Kynurenine Pathway: Implications and Therapeutic Prospects in Alzheimer's Disease

por Adeyemi, Oluyomi Stephen, Awakan, Oluwakemi Josephine, Afolabi, Lawrence Boluwatife, Rotimi, Damilare Emmanuel, Oluwayemi, Elizabeth, Otuechere, Chiagoziem A., Ibraheem, Omodele, Elebiyo, Tobiloba Chritiana, Alejolowo, Omokolade, Arowolo, Afolake T.
Publicado 2021