Lysosomal Interaction of Akt with Phafin2: A Critical Step in the Induction of Autophagy

od Matsuda-Lennikov, Mami, Suizu, Futoshi, Hirata, Noriyuki, Hashimoto, Manabu, Kimura, Kohki, Nagamine, Tadashi, Fujioka, Yoichiro, Ohba, Yusuke, Iwanaga, Toshihiko, Noguchi, Masayuki
Wydane 2014

Functional characterization of lysosomal interaction of Akt with VRK2

od Hirata, Noriyuki, Suizu, Futoshi, Matsuda-Lennikov, Mami, Tanaka, Tsutomu, Edamura, Tatsuma, Ishigaki, Satoko, Donia, Thoria, Lithanatudom, Pathrapol, Obuse, Chikashi, Iwanaga, Toshihiko, Noguchi, Masayuki
Wydane w Oncogene (2018)

Magnesium transporter 1 (MAGT1) deficiency causes selective defects in N-linked glycosylation and expression of immune-response genes

od Matsuda-Lennikov, Mami, Biancalana, Matthew, Zou, Juan, Ravell, Juan C., Zheng, Lixin, Kanellopoulou, Chrysi, Jiang, Ping, Notarangelo, Giulia, Jing, Huie, Masutani, Evan, Oler, Andrew J., Olano, Lisa Renee, Schulz, Benjamin L., Lenardo, Michael J.
Wydane w J Biol Chem (2019)

Mg(2+) regulation of kinase signaling and immune function

od Kanellopoulou, Chryssa, George, Alex B., Masutani, Evan, Cannons, Jennifer L., Ravell, Juan C., Yamamoto, Tori N., Smelkinson, Margery G., Jiang, Ping Du, Matsuda-Lennikov, Mami, Reilley, Julie, Handon, Robin, Lee, Ping-Hsien, Miller, J. Richard, Restifo, Nicholas P., Zheng, Lixin, Schwartzberg, Pamela L., Young, Matthew, Lenardo, Michael J.
Wydane w J Exp Med (2019)

Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency

od Abolhassani, Hassan, Edwards, Emily S.J., Ikinciogullari, Aydan, Jing, Huie, Borte, Stephan, Buggert, Marcus, Du, Likun, Matsuda-Lennikov, Mami, Romano, Rosa, Caridha, Rozina, Bade, Sangeeta, Zhang, Yu, Frederiksen, Juliet, Fang, Mingyan, Bal, Sevgi Kostel, Haskologlu, Sule, Dogu, Figen, Tacyildiz, Nurdan, Matthews, Helen F., McElwee, Joshua J., Gostick, Emma, Price, David A., Palendira, Umaimainthan, Aghamohammadi, Asghar, Boisson, Bertrand, Rezaei, Nima, Karlsson, Annika C., Lenardo, Michael J., Casanova, Jean-Laurent, Hammarström, Lennart, Tangye, Stuart G., Su, Helen C., Pan-Hammarström, Qiang
Wydane w J Exp Med (2017)

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

od Ravell, Juan C., Matsuda-Lennikov, Mami, Chauvin, Samuel D., Zou, Juan, Biancalana, Matthew, Deeb, Sally J., Price, Susan, Su, Helen C., Notarangelo, Giulia, Jiang, Ping, Morawski, Aaron, Kanellopoulou, Chrysi, Binder, Kyle, Mukherjee, Ratnadeep, Anibal, James T., Sellers, Brian, Zheng, Lixin, He, Tingyan, George, Alex B., Pittaluga, Stefania, Powers, Astin, Kleiner, David E., Kapuria, Devika, Ghany, Marc, Hunsberger, Sally, Cohen, Jeffrey I., Uzel, Gulbu, Bergerson, Jenna, Wolfe, Lynne, Toro, Camilo, Gahl, William, Folio, Les R., Matthews, Helen, Angelus, Pam, Chinn, Ivan K., Orange, Jordan S., Trujillo-Vargas, Claudia M., Franco, Jose Luis, Orrego-Arango, Julio, Gutiérrez-Hincapié, Sebastian, Patel, Niraj Chandrakant, Raymond, Kimiyo, Patiroglu, Turkan, Unal, Ekrem, Karakukcu, Musa, Day, Alexandre G.R., Mehta, Pankaj, Masutani, Evan, De Ravin, Suk S., Malech, Harry L., Altan-Bonnet, Grégoire, Rao, V. Koneti, Mann, Matthias, Lenardo, Michael J.
Wydane w J Clin Invest (2019)