Gene Therapies for Primary Immune Deficiencies

por Kohn, Lisa A., Kohn, Donald B.
Publicado 2021

Novel Compound Heterozygote Variations in FADD Identified to Cause FAS-Associated Protein with Death Domain Deficiency

por Kohn, Lisa A., Long, Joseph D., Trope, Edward C., Kuo, Caroline Y.
Publicado 2020

Systematic screens of a Candida albicans homozygous deletion library decouple morphogenetic switching and pathogenicity

por Noble, Suzanne M., French, Sarah, Kohn, Lisa A., Chen, Victoria, Johnson, Alexander D.
Publicado 2010

Ocular findings associated with FADD deficiency resemble familial exudative vitreoretinopathy

por Meer, Elana, Solanes, Federica, Kohn, Lisa, Kuo, Caroline Y., Wong, Derek A., Pineles, Stacy, Tsui, Irena
Publicado 2022

Commercial immunoglobulin products contain cross-reactive but not neutralizing antibodies against SARS-CoV-2

por Ahn, Terrie S., Han, Brandon, Krogstad, Paul, Bun, Chantana, Kohn, Lisa A., Garcia-Lloret, Maria I., Damoiseaux, Robert, Butte, Manish J.
Publicado 2021

Lymphoid Priming in Human Bone Marrow Begins Prior to CD10 Expression with Up-Regulation of L-selectin

por Kohn, Lisa A., Hao, Qian-Lin, Sasidharan, Rajkumar, Parekh, Chintan, Ge, Shundi, Zhu, Yuhua, Mikkola, Hanna K.A., Crooks, Gay M.
Publicado 2012

Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

por Béziat, Vivien, Tavernier, Simon J., Chen, Yin-Huai, Ma, Cindy S., Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A., De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Luxman Maglorius Renkilaraj, Majistor Raj, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A., Dai, Hongzheng, Burrage, Lindsay C., Murdock, David R., Lambrecht, Bart N., Avettand-Fenoel, Véronique, Vogel, Tiphanie P., Network, Undiagnosed Diseases, Esther, Charles R., Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D., Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J., Freeman, Alexandra F., Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A., Tangye, Stuart G., Uhlig, Holm H., Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne
Publicado 2020

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

por Béziat, Vivien, Tavernier, Simon J., Chen, Yin-Huai, Ma, Cindy S., Materna, Marie, Laurence, Arian, Staal, Jens, Aschenbrenner, Dominik, Roels, Lisa, Worley, Lisa, Claes, Kathleen, Gartner, Lisa, Kohn, Lisa A., De Bruyne, Marieke, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Keles, Sevgi, Nammour, Justine, Vladikine, Natasha, Maglorius Renkilaraj, Majistor Raj Luxman, Seeleuthner, Yoann, Migaud, Mélanie, Rosain, Jérémie, Jeljeli, Mohamed, Boisson, Bertrand, Van Braeckel, Eva, Rosenfeld, Jill A., Dai, Hongzheng, Burrage, Lindsay C., Murdock, David R., Lambrecht, Bart N., Avettand-Fenoel, Véronique, Vogel, Tiphanie P., Esther, Charles R., Haskologlu, Sule, Dogu, Figen, Ciznar, Peter, Boutboul, David, Ouachée-Chardin, Marie, Amourette, Jean, Lebras, Marie-Noëlle, Gauvain, Clément, Tcherakian, Colas, Ikinciogullari, Aydan, Beyaert, Rudi, Abel, Laurent, Milner, Joshua D., Grimbacher, Bodo, Couderc, Louis-Jean, Butte, Manish J., Freeman, Alexandra F., Catherinot, Émilie, Fieschi, Claire, Chatila, Talal A., Tangye, Stuart G., Uhlig, Holm H., Haerynck, Filomeen, Casanova, Jean-Laurent, Puel, Anne
Publicado 2020