檢索結果 - Ehlayel, Mohammed

A Novel STAT3 Mutation in a Qatari Patient With Hyper-IgE Syndrome 由 Chaimowitz, Natalia S., Branch, Justin, Reyes, Anaid, Vargas-Hernández, Alexander, Orange, Jordan S., Forbes, Lisa R., Ehlayel, Mohammed, Purayil, Saleema C., Al-Nesf, Maryam Ali, Vogel, Tiphanie P.

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Novel aspects of Kindlin-3 function in humans based on a new case of Leukocyte Adhesion Deficiency III (LAD-III) 由 Meller, Julia, Malinin, Nikolay L., Panigrahi, Soumya, Kerr, Bethany A., Patil, Arohi, Ma, Yi, Venkateswaran, Lakshmi, Rogozin, Igor B., Mohandas, Narla, Ehlayel, Mohammed S., Podrez, Eugene A., Chinen, Javier, Byzova, Tatiana V.

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Mutations in PI3K110δ cause impaired NK cell function partially rescued by rapamycin treatment 由 Ruiz-García, Raquel, Vargas-Hernandez, Alexander, Chinn, Ivan K., Angelo, Laura S., Cao, Tram N., Coban-Akdemir, Zeynep, Jhangiani, Shalini N., Meng, Qingchang, Forbes, Lisa R., Muzny, Donna M., Allende, Luis M., Ehlayel, Mohammed S., Gibbs, Richard A., Lupski, James R., Uzel, Gulbu, Orange, Jordan S., Mace, Emily M.

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