The T-box transcription factor, TBX3, is a key substrate of AKT3 in melanomagenesis

por Peres, Jade, Mowla, Shaheen, Prince, Sharon
Publicado 2014

Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease

por Pule, Gift Dineo, Mowla, Shaheen, Novitzky, Nicolas, Wonkam, Ambroise
Publicado 2016

Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon

por Wonkam, Ambroise, Lebeko, Kamogelo, Mowla, Shaheen, Noubiap, Jean Jacques, Chong, Mike, Pare, Guillaume
Publicado 2021

HIV-1 Transactivator of Transcription (Tat) Co-operates With AP-1 Factors to Enhance c-MYC Transcription

por Alves de Souza Rios, Leonardo, Mapekula, Lungile, Mdletshe, Nontlantla, Chetty, Dharshnee, Mowla, Shaheen
Publicado 2021

Modulation of Cellular MicroRNA by HIV-1 in Burkitt Lymphoma Cells—A Pathway to Promoting Oncogenesis

por Ramorola, Beatrice Relebogile, Goolam-Hoosen, Taahira, Alves de Souza Rios, Leonardo, Mowla, Shaheen
Publicado 2021

Chemoresistance to Cancer Treatment: Benzo-α-Pyrene as Friend or Foe?

por Dzobo, Kevin, Hassen, Naseeha, Senthebane, Dimakatso Alice, Thomford, Nicholas Ekow, Rowe, Arielle, Shipanga, Hendrina, Wonkam, Ambroise, Parker, M. Iqbal, Mowla, Shaheen, Dandara, Collet
Publicado 2018

Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment

por Wonkam-Tingang, Edmond, Schrauwen, Isabelle, Esoh, Kevin K., Bharadwaj, Thashi, Nouel-Saied, Liz M., Acharya, Anushree, Nasir, Abdul, Adadey, Samuel M., Mowla, Shaheen, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2020

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Alves de Souza Rios, Leonardo, Aboagye, Elvis Twumasi, Esoh, Kevin, Manyisa, Noluthando, De Kock, Carmen, Awandare, Gordon A., Mowla, Shaheen, Wonkam, Ambroise
Publicado 2022

Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

por Adadey, Samuel M., Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Bharadwaj, Thashi, Esoh, Kevin K., Basit, Sulman, Acharya, Anushree, Nouel-Saied, Liz M., Liaqat, Khurram, Wonkam-Tingang, Edmond, Mowla, Shaheen, Awandare, Gordon A., Ahmad, Wasim, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2021

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

por Manyisa, Noluthando, Schrauwen, Isabelle, de Souza Rios, Leonardo Alves, Mowla, Shaheen, Tekendo-Ngongang, Cedrik, Popel, Kalinka, Esoh, Kevin, Bharadwaj, Thashi, Nouel-Saied, Liz M., Acharya, Anushree, Nasir, Abdul, Wonkam-Tingang, Edmond, de Kock, Carmen, Dandara, Collet, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2021