Pesquisa | Portal de Pesquisa da BVS

1.

Genetics of Pediatric Immune-Mediated Diseases and Human Immunity.

Schmitt, Erica G; Cooper, Megan A.

Annu Rev Immunol ; 39: 227-249, 2021 04 26.

Artigo em Inglês | MEDLINE | ID: mdl-33534603

2.

STAT3 gain-of-function mutations connect leukemia with autoimmune disease by pathological NKG2D^hi CD8⁺ T cell dysregulation and accumulation.

Masle-Farquhar, Etienne; Jackson, Katherine J L; Peters, Timothy J; Al-Eryani, Ghamdan; Singh, Mandeep; Payne, Kathryn J; Rao, Geetha; Avery, Danielle T; Apps, Gabrielle; Kingham, Jennifer; Jara, Christopher J; Skvortsova, Ksenia; Swarbrick, Alexander; Ma, Cindy S; Suan, Daniel; Uzel, Gulbu; Chua, Ignatius; Leiding, Jennifer W; Heiskanen, Kaarina; Preece, Kahn; Kainulainen, Leena; O'Sullivan, Michael; Cooper, Megan A; Seppänen, Mikko R J; Mustjoki, Satu; Brothers, Shannon; Vogel, Tiphanie P; Brink, Robert; Tangye, Stuart G; Reed, Joanne H; Goodnow, Christopher C.

Immunity ; 55(12): 2386-2404.e8, 2022 12 13.

Artigo em Inglês | MEDLINE | ID: mdl-36446385

3.

MicroRNA-142 Is Critical for the Homeostasis and Function of Type 1 Innate Lymphoid Cells.

Berrien-Elliott, Melissa M; Sun, Yaping; Neal, Carly; Ireland, Aaron; Trissal, Maria C; Sullivan, Ryan P; Wagner, Julia A; Leong, Jeffrey W; Wong, Pamela; Mah-Som, Annelise Y; Wong, Terrence N; Schappe, Timothy; Keppel, Catherine R; Cortez, Victor S; Stamatiades, Efstathios G; Li, Ming O; Colonna, Marco; Link, Daniel C; French, Anthony R; Cooper, Megan A; Wang, Wei-Le; Boldin, Mark P; Reddy, Pavan; Fehniger, Todd A.

Immunity ; 51(3): 479-490.e6, 2019 09 17.

Artigo em Inglês | MEDLINE | ID: mdl-31402259

4.

Somatic mosaicism in inborn errors of immunity: Current knowledge, challenges, and future perspectives.

Aluri, Jahnavi; Cooper, Megan A.

Semin Immunol ; 67: 101761, 2023 05.

Artigo em Inglês | MEDLINE | ID: mdl-37062181

5.

Comment on: Evidence of innate lymphoid cell redundancy in humans.

Orange, Jordan S; Mace, Emily M; French, Anthony R; Yokoyama, Wayne M; Fehniger, Todd A; Cooper, Megan A.

Nat Immunol ; 19(8): 788-789, 2018 08.

Artigo em Inglês | MEDLINE | ID: mdl-30026477

6.

Teach Your NK Cells Well.

Cooper, Megan A.

Immunity ; 45(2): 229-31, 2016 08 16.

Artigo em Inglês | MEDLINE | ID: mdl-27533007

7.

Deficiencies and Dysregulation of STAT Pathways That Drive Inborn Errors of Immunity: Lessons from Patients and Mouse Models of Disease.

Toth, Kelsey A; Schmitt, Erica G; Cooper, Megan A.

J Immunol ; 210(10): 1463-1472, 2023 05 15.

Artigo em Inglês | MEDLINE | ID: mdl-37126806

8.

IL-15 Priming Alters IFN-Î³ Regulation in Murine NK Cells.

Cimpean, Maria; Keppel, Molly P; Gainullina, Anastasiia; Fan, Changxu; Sohn, Hyogon; Schedler, Nathan C; Swain, Amanda; Kolicheski, Ana; Shapiro, Hannah; Young, Howard A; Wang, Ting; Artyomov, Maxim N; Cooper, Megan A.

J Immunol ; 211(10): 1481-1493, 2023 11 15.

Artigo em Inglês | MEDLINE | ID: mdl-37747317

9.

MYSM1 attenuates DNA damage signals triggered by physiologic and genotoxic DNA breaks.

Mathias, Brendan; O'Leary, David; Saucier, Nermina; Ahmad, Faiz; White, Lynn S; Russell, Le'Mark; Shinawi, Marwan; Smith, Matthew J; Abraham, Roshini S; Cooper, Megan A; Kitcharoensakkul, Maleewan; Green, Abby M; Bednarski, Jeffrey J.

J Allergy Clin Immunol ; 153(4): 1113-1124.e7, 2024 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-38065233

10.

Human PLCG2 haploinsufficiency results in a novel natural killer cell immunodeficiency.

Alinger, Joshua B; Mace, Emily M; Porter, Justin R; Mah-Som, Annelise Y; Daugherty, Allyssa L; Li, Stephanie; Throm, Allison A; Pingel, Jeanette T; Saucier, Nermina; Yao, Albert; Chinn, Ivan K; Lupski, James R; Ehlayel, Mohammad; Keller, Michael; Bowman, Greg R; Cooper, Megan A; Orange, Jordan S; French, Anthony R.

J Allergy Clin Immunol ; 153(1): 216-229, 2024 01.

Artigo em Inglês | MEDLINE | ID: mdl-37714437

11.

Management of Atopy with Dupilumab and Omalizumab in CADINS Disease.

Diaz-Cabrera, Natalie M; Bauman, Bradly M; Iro, Mildred A; Dabbah-Krancher, Gina; Molho-Pessach, Vered; Zlotogorski, Abraham; Shamriz, Oded; Dinur-Schejter, Yael; Sharon, Tatyana Dubnikov; Stepensky, Polina; Tal, Yuval; Eisenstein, Eli M; Pietzsch, Leonora; Schuetz, Catharina; Abreu, Damien; Coughlin, Carrie C; Cooper, Megan A; Milner, Joshua D; Williams, Anthony; Armoni-Weiss, Gil; Snow, Andrew L; Leiding, Jennifer W.

J Clin Immunol ; 44(2): 48, 2024 Jan 17.

Artigo em Inglês | MEDLINE | ID: mdl-38231347

12.

Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue.

Sharma, Richa; Sahoo, Sushree S; Honda, Masayoshi; Granger, Sophie L; Goodings, Charnise; Sanchez, Louis; Künstner, Axel; Busch, Hauke; Beier, Fabian; Pruett-Miller, Shondra M; Valentine, Marcus B; Fernandez, Alfonso G; Chang, Ti-Cheng; Géli, Vincent; Churikov, Dmitri; Hirschi, Sandrine; Pastor, Victor B; Boerries, Melanie; Lauten, Melchior; Kelaidi, Charikleia; Cooper, Megan A; Nicholas, Sarah; Rosenfeld, Jill A; Polychronopoulou, Sophia; Kannengiesser, Caroline; Saintomé, Carole; Niemeyer, Charlotte M; Revy, Patrick; Wold, Marc S; Spies, Maria; Erlacher, Miriam; Coulon, Stéphane; Wlodarski, Marcin W.

Blood ; 139(7): 1039-1051, 2022 02 17.

Artigo em Inglês | MEDLINE | ID: mdl-34767620

13.

Multiplexed Functional Assessment of Genetic Variants in CARD11.

Meitlis, Iana; Allenspach, Eric J; Bauman, Bradly M; Phan, Isabelle Q; Dabbah, Gina; Schmitt, Erica G; Camp, Nathan D; Torgerson, Troy R; Nickerson, Deborah A; Bamshad, Michael J; Hagin, David; Luthers, Christopher R; Stinson, Jeffrey R; Gray, Jessica; Lundgren, Ingrid; Church, Joseph A; Butte, Manish J; Jordan, Mike B; Aceves, Seema S; Schwartz, Daniella M; Milner, Joshua D; Schuval, Susan; Skoda-Smith, Suzanne; Cooper, Megan A; Starita, Lea M; Rawlings, David J; Snow, Andrew L; James, Richard G.

Am J Hum Genet ; 107(6): 1029-1043, 2020 12 03.

Artigo em Inglês | MEDLINE | ID: mdl-33202260

14.

Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function.

Aluri, Jahnavi; Bach, Alicia; Kaviany, Saara; Chiquetto Paracatu, Luana; Kitcharoensakkul, Maleewan; Walkiewicz, Magdalena A; Putnam, Christopher D; Shinawi, Marwan; Saucier, Nermina; Rizzi, Elise M; Harmon, Michael T; Keppel, Molly P; Ritter, Michelle; Similuk, Morgan; Kulm, Elaine; Joyce, Michael; de Jesus, Adriana A; Goldbach-Mansky, Raphaela; Lee, Yi-Shan; Cella, Marina; Kendall, Peggy L; Dinauer, Mary C; Bednarski, Jeffrey J; Bemrich-Stolz, Christina; Canna, Scott W; Abraham, Shirley M; Demczko, Matthew M; Powell, Jonathan; Jones, Stacie M; Scurlock, Amy M; De Ravin, Suk See; Bleesing, Jack J; Connelly, James A; Rao, V Koneti; Schuettpelz, Laura G; Cooper, Megan A.

Blood ; 137(18): 2450-2462, 2021 05 06.

Artigo em Inglês | MEDLINE | ID: mdl-33512449

15.

Descriptive analysis evaluating the use of direct oral anticoagulation therapy in heart and lung transplant recipients.

Rubido, Eric D; Cooper, Megan H; Donahue, Kevin R; Krisl, Jill.

Clin Transplant ; 37(2): e14897, 2023 02.

Artigo em Inglês | MEDLINE | ID: mdl-36585934

16.

STAT3 Gain-of-Function Mutations Underlie Deficiency in Human Nonclassical CD16⁺ Monocytes and CD141⁺ Dendritic Cells.

Korenfeld, Daniel; Roussak, Kate; Dinkel, Sabrina; Vogel, Tiphanie P; Pollack, Henry; Levy, Joseph; Leiding, Jennifer W; Milner, Joshua; Cooper, Megan; Klechevsky, Eynav.

J Immunol ; 207(10): 2423-2432, 2021 11 15.

Artigo em Inglês | MEDLINE | ID: mdl-34654687

17.

Understanding the barriers and facilitators related to birthing pool use from organisational and multi-professional perspectives: a mixed-methods systematic review.

Cooper, Megan; Madeley, Anna-Marie; Burns, Ethel; Feeley, Claire.

Reprod Health ; 20(1): 147, 2023 Oct 04.

Artigo em Inglês | MEDLINE | ID: mdl-37794365

18.

Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.

Bosticardo, Marita; Yamazaki, Yasuhiro; Cowan, Jennifer; Giardino, Giuliana; Corsino, Cristina; Scalia, Giulia; Prencipe, Rosaria; Ruffner, Melanie; Hill, David A; Sakovich, Inga; Yemialyanava, Irma; Tam, Jonathan S; Padem, Nurcicek; Elder, Melissa E; Sleasman, John W; Perez, Elena; Niebur, Hana; Seroogy, Christine M; Sharapova, Svetlana; Gebbia, Jennifer; Kleiner, Gary Ira; Peake, Jane; Abbott, Jordan K; Gelfand, Erwin W; Crestani, Elena; Biggs, Catherine; Butte, Manish J; Hartog, Nicholas; Hayward, Anthony; Chen, Karin; Heimall, Jennifer; Seeborg, Filiz; Bartnikas, Lisa M; Cooper, Megan A; Pignata, Claudio; Bhandoola, Avinash; Notarangelo, Luigi D.

Am J Hum Genet ; 105(3): 549-561, 2019 09 05.

Artigo em Inglês | MEDLINE | ID: mdl-31447097

19.

TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins.

Fejtkova, Martina; Sukova, Martina; Hlozkova, Katerina; Skvarova Kramarzova, Karolina; Rackova, Marketa; Jakubec, David; Bakardjieva, Marina; Bloomfield, Marketa; Klocperk, Adam; Parackova, Zuzana; Sediva, Anna; Aluri, Jahnavi; Novakova, Michaela; Kalina, Tomas; Fronkova, Eva; Hrusak, Ondrej; Malcova, Hana; Sedlacek, Petr; Liba, Zuzana; Kudr, Martin; Stary, Jan; Cooper, Megan A; Svaton, Michael; Kanderova, Veronika.

Am J Hematol ; 97(3): 338-351, 2022 03 01.

Artigo em Inglês | MEDLINE | ID: mdl-34981838

20.

Genetic Mosaicism as a Cause of Inborn Errors of Immunity.