Novel mechanisms control the folding and assembly of λ5/14.1 and VpreB to produce an intact surrogate light chain

por Minegishi, Yoshiyuki, Hendershot, Linda M., Conley, Mary Ellen
Publicado 1999

Mutations in Igα (CD79a) result in a complete block in B-cell development

por Minegishi, Yoshiyuki, Coustan-Smith, Elaine, Rapalus, Lisa, Ersoy, Fügen, Campana, Dario, Conley, Mary Ellen
Publicado 1999

Mutations in the Human λ5/14.1 Gene Result in B Cell Deficiency and Agammaglobulinemia

por Minegishi, Yoshiyuki, Coustan-Smith, Elaine, Wang, Yui-Hsi, Cooper, Max D., Campana, Dario, Conley, Mary Ellen
Publicado 1998

Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development

por Mitsui, Silvia Naomi, Yasue, Akihiro, Masuda, Kiyoshi, Naruto, Takuya, Minegishi, Yoshiyuki, Oyadomari, Seiichi, Noji, Sumihare, Imoto, Issei, Tanaka, Eiji
Publicado en Sci Rep (2016)

The skin is an important bulwark of acquired immunity against intestinal helminths

por Obata-Ninomiya, Kazushige, Ishiwata, Kenji, Tsutsui, Hidemitsu, Nei, Yuichiro, Yoshikawa, Soichiro, Kawano, Yohei, Minegishi, Yoshiyuki, Ohta, Nobuo, Watanabe, Naohiro, Kanuka, Hirotaka, Karasuyama, Hajime
Publicado 2013

Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome

por Minegishi, Yoshiyuki, Saito, Masako, Nagasawa, Masayuki, Takada, Hidetoshi, Hara, Toshiro, Tsuchiya, Shigeru, Agematsu, Kazunaga, Yamada, Masafumi, Kawamura, Nobuaki, Ariga, Tadashi, Tsuge, Ikuya, Karasuyama, Hajime
Publicado 2009

Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cells

por Saito, Masako, Nagasawa, Masayuki, Takada, Hidetoshi, Hara, Toshiro, Tsuchiya, Shigeru, Agematsu, Kazunaga, Yamada, Masafumi, Kawamura, Nobuaki, Ariga, Tadashi, Tsuge, Ikuya, Nonoyama, Shigeaki, Karasuyama, Hajime, Minegishi, Yoshiyuki
Publicado 2011

Selective ablation of basophils in mice reveals their nonredundant role in acquired immunity against ticks

por Wada, Takeshi, Ishiwata, Kenji, Koseki, Haruhiko, Ishikura, Tomoyuki, Ugajin, Tsukasa, Ohnuma, Naotsugu, Obata, Kazushige, Ishikawa, Ryosuke, Yoshikawa, Soichiro, Mukai, Kaori, Kawano, Yohei, Minegishi, Yoshiyuki, Yokozeki, Hiroo, Watanabe, Naohiro, Karasuyama, Hajime
Publicado 2010

Functional STAT3 deficiency compromises the generation of human T follicular helper cells

por Ma, Cindy S., Avery, Danielle T., Chan, Anna, Batten, Marcel, Bustamante, Jacinta, Boisson-Dupuis, Stephanie, Arkwright, Peter D., Kreins, Alexandra Y., Averbuch, Diana, Engelhard, Dan, Magdorf, Klaus, Kilic, Sara S., Minegishi, Yoshiyuki, Nonoyama, Shigeaki, French, Martyn A., Choo, Sharon, Smart, Joanne M., Peake, Jane, Wong, Melanie, Gray, Paul, Cook, Matthew C., Fulcher, David A., Casanova, Jean-Laurent, Deenick, Elissa K., Tangye, Stuart G.
Publicado 2012

Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4(+) T cells into distinct effector subsets

por Ma, Cindy S., Wong, Natalie, Rao, Geetha, Nguyen, Akira, Avery, Danielle T., Payne, Kathryn, Torpy, James, O’Young, Patrick, Deenick, Elissa, Bustamante, Jacinta, Puel, Anne, Okada, Satoshi, Kobayashi, Masao, Martinez-Barricarte, Ruben, Elliott, Michael, Sebnem Kilic, Sara, El Baghdadi, Jamila, Minegishi, Yoshiyuki, Bousfiha, Aziz, Robertson, Nic, Hambleton, Sophie, Arkwright, Peter D., French, Martyn, Blincoe, Annaliesse K., Hsu, Peter, Campbell, Dianne E., Stormon, Michael O., Wong, Melanie, Adelstein, Stephen, Fulcher, David A., Cook, Matthew C., Stepensky, Polina, Boztug, Kaan, Beier, Rita, Ikincioğullari, Aydan, Ziegler, John B., Gray, Paul, Picard, Capucine, Boisson-Dupuis, Stéphanie, Phan, Tri Giang, Grimbacher, Bodo, Warnatz, Klaus, Holland, Steven M., Uzel, Gulbu, Casanova, Jean-Laurent, Tangye, Stuart G.
Publicado en J Exp Med (2016)

Monogenic mutations differentially impact the quantity and quality of T follicular helper cells in human primary immunodeficiencies

por Ma, Cindy S, Wong, Natalie, Rao, Geetha, Avery, Danielle T, Torpy, James, Hambridge, Thomas, Bustamante, Jacinta, Okada, Satoshi, Stoddard, Jennifer L, Deenick, Elissa K, Pelham, Simon J, Payne, Katherine, Boisson-Dupuis, Stéphanie, Puel, Anne, Kobayashi, Masao, Arkwright, Peter D, Kilic, Sara Sebnem, Baghdadi, Jamila El, Nonoyama, Shigeaki, Minegishi, Yoshiyuki, Mahdaviani, Seyed Alireza, Mansouri, Davood, Bousfiha, Aziz, Blincoe, Annaliesse K, French, Martyn A, Hsu, Peter, Campbell, Dianne E., Stormon, Michael O, Wong, Melanie, Adelstein, Stephen, Smart, Joanne M, Fulcher, David A, Cook, Matthew C, Phan, Tri G, Stepensky, Polina, Boztug, Kaan, Kansu, Aydan, Ikincioğullari, Aydan, Baumann, Ulrich, Beier, Rita, Roscioli, Tony, Ziegler, John B, Gray, Paul, Picard, Capucine, Grimbacher, Bodo, Warnatz, Klaus, Holland, Steven M, Casanova, Jean-Laurent, Uzel, Gulbu, Tangye, Stuart G
Publicado en J Allergy Clin Immunol (2015)

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

por Kreins, Alexandra Y., Ciancanelli, Michael J., Okada, Satoshi, Kong, Xiao-Fei, Ramírez-Alejo, Noé, Kilic, Sara Sebnem, El Baghdadi, Jamila, Nonoyama, Shigeaki, Mahdaviani, Seyed Alireza, Ailal, Fatima, Bousfiha, Aziz, Mansouri, Davood, Nievas, Elma, Ma, Cindy S., Rao, Geetha, Bernasconi, Andrea, Sun Kuehn, Hye, Niemela, Julie, Stoddard, Jennifer, Deveau, Paul, Cobat, Aurelie, El Azbaoui, Safa, Sabri, Ayoub, Lim, Che Kang, Sundin, Mikael, Avery, Danielle T., Halwani, Rabih, Grant, Audrey V., Boisson, Bertrand, Bogunovic, Dusan, Itan, Yuval, Moncada-Velez, Marcela, Martinez-Barricarte, Ruben, Migaud, Melanie, Deswarte, Caroline, Alsina, Laia, Kotlarz, Daniel, Klein, Christoph, Muller-Fleckenstein, Ingrid, Fleckenstein, Bernhard, Cormier-Daire, Valerie, Rose-John, Stefan, Picard, Capucine, Hammarstrom, Lennart, Puel, Anne, Al-Muhsen, Saleh, Abel, Laurent, Chaussabel, Damien, Rosenzweig, Sergio D., Minegishi, Yoshiyuki, Tangye, Stuart G., Bustamante, Jacinta, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie
Publicado en J Exp Med (2015)