X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase

por Agrebi, Nourhen, Gentilcore, Giusy, Grivel, Jean-Charles, Alkhayer, Ghroob, Hassoun, Jihad, Hassan, Amel, Adeli, Mehdi, Lo, Bernice
Publicado 2021

Novel ORAI1 Mutation Disrupts Channel Trafficking Resulting in Combined Immunodeficiency

por Yu, Fang, Agrebi, Nourhen, Mackeh, Rafah, Abouhazima, Khaled, KhudaBakhsh, Khadija, Adeli, Mehdi, Lo, Bernice, Hassan, Amel, Machaca, Khaled
Publicado 2021

Case Report: FOXP3 Mutation in a Patient Presenting With ALPS

por Rais, Afef, Mekki, Najla, Fedhila, Faten, Alosaimi, Mohammed Faraj, Ben Khaled, Monia, Zameli, Amal, Agrebi, Nourhen, Sellami, Maryam Kallel, Geha, Raif, Ben-Mustapha, Imen, Barbouche, Mohamed-Ridha
Publicado 2021

In vitro Interleukin-7 treatment partially rescues MAIT cell dysfunction caused by SARS-CoV-2 infection

por Hubrack, Satanay, Al-Nesf, Maryam Ali, Agrebi, Nourhen, Raynaud, Christophe, Khattab, Mohammed Abu, Thomas, Merlin, Ibrahim, Tayseer, Taha, Salma, Dermime, Said, Merhi, Maysaloun, Kulinski, Michal, Steinhoff, Martin, Tang, Patrick, Lo, Bernice
Publicado 2021

Human AGR2 Deficiency Causes Mucus Barrier Dysfunction and Infantile Inflammatory Bowel Disease

por Al-Shaibi, Ahmad A., Abdel-Motal, Ussama M., Hubrack, Satanay Z., Bullock, Alex N., Al-Marri, Amna A., Agrebi, Nourhen, Al-Subaiey, Abdulrahman A., Ibrahim, Nazira A., Charles, Adrian K., Elawad, Mamoun, Uhlig, Holm H., Lo, Bernice
Publicado 2021