日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Clinical, immunologic, and genetic characteristics of 148 patients with natural killer cell deficiency

148例自然杀伤细胞缺陷患者的临床、免疫学和遗传学特征

Abdalgani, Manar; Hernandez, Evelyn R; Pedroza, Luis A; Chinn, Ivan K; Forbes Satter, Lisa R; Rider, Nicholas L; Banerjee, Pinaki P; Poli, M Cecilia; Mahapatra, Sanjana; Canter, Debra; Cao, Tram; Shawver, Linda M; Nandiwada, Sarada L; Lupski, James R; Posey, Jennifer E; Ramakrishnan, Rajasekhar; Mace, Emily M; Orange, Jordan S

Inborn errors of immunity reveal molecular requirements for generation and maintenance of human CD4(+) IL-9-expressing cells

先天性免疫缺陷揭示了人类CD4(+)IL-9表达细胞生成和维持的分子需求

Rao, Geetha; Mack, Corinne D; Nguyen, Tina; Wong, Natalie; Payne, Kathryn; Worley, Lisa; Gray, Paul E; Wong, Melanie; Hsu, Peter; Stormon, Michael O; Preece, Kahn; Suan, Daniel; O'Sullivan, Michael; Blincoe, Annaliesse K; Sinclair, Jan; Okada, Satoshi; Hambleton, Sophie; Arkwright, Peter D; Boztug, Kaan; Stepensky, Polina; Cooper, Megan A; Bezrodnik, Liliana; Nadeau, Kari C; Abolhassani, Hassan; Abraham, Roshini S; Seppänen, Mikko R J; Béziat, Vivien; Bustamante, Jacinta; Forbes Satter, Lisa R; Leiding, Jennifer W; Meyts, Isabelle; Jouanguy, Emmanuelle; Boisson-Dupuis, Stéphanie; Uzel, Gulbu; Puel, Anne; Casanova, Jean-Laurent; Tangye, Stuart G; Ma, Cindy S

Posttransplantation late complications increase over time for patients with SCID: A Primary Immune Deficiency Treatment Consortium (PIDTC) landmark study

移植后晚期并发症在重症联合免疫缺陷病(SCID)患者中随时间推移而增加:一项原发性免疫缺陷治疗联盟(PIDTC)里程碑式研究

Eissa, Hesham; Thakar, Monica S; Shah, Ami J; Logan, Brent R; Griffith, Linda M; Dong, Huaying; Parrott, Roberta E; O'Reilly, Richard J; Dara, Jasmeen; Kapoor, Neena; Forbes Satter, Lisa; Chandra, Sharat; Kapadia, Malika; Chandrakasan, Shanmuganathan; Knutsen, Alan; Jyonouchi, Soma C; Molinari, Lyndsay; Rayes, Ahmad; Ebens, Christen L; Teira, Pierre; Dávila Saldaña, Blachy J; Burroughs, Lauri M; Chaudhury, Sonali; Chellapandian, Deepak; Gillio, Alfred P; Goldman, Fredrick; Malech, Harry L; DeSantes, Kenneth; Cuvelier, Geoff D E; Rozmus, Jacob; Quinones, Ralph; Yu, Lolie C; Broglie, Larisa; Aquino, Victor; Shereck, Evan; Moore, Theodore B; Vander Lugt, Mark T; Mousallem, Talal I; Oved, Joeseph H; Dorsey, Morna; Abdel-Azim, Hisham; Martinez, Caridad; Bleesing, Jacob H; Prockop, Susan; Kohn, Donald B; Bednarski, Jeffrey J; Leiding, Jennifer; Marsh, Rebecca A; Torgerson, Troy; Notarangelo, Luigi D; Pai, Sung-Yun; Pulsipher, Michael A; Puck, Jennifer M; Dvorak, Christopher C; Haddad, Elie; Buckley, Rebecca H; Cowan, Morton J; Heimall, Jennifer

Genotype, oxidase status, and preceding infection or autoinflammation do not affect allogeneic HCT outcomes for CGD

基因型、氧化酶状态以及既往感染或自身炎症均不影响慢性肉芽肿病(CGD)患者的异基因造血干细胞移植(HCT)预后。

Leiding, Jennifer W; Arnold, Danielle E; Parikh, Suhag; Logan, Brent; Marsh, Rebecca A; Griffith, Linda M; Wu, Ruizhe; Kidd, Sharon; Mallhi, Kanwaldeep; Chellapandian, Deepak; Si Lim, Stephanie J; Grunebaum, Eyal; Falcone, E Liana; Murguia-Favela, Luis; Grossman, Debbi; Prasad, Vinod K; Heimall, Jennifer R; Touzot, Fabien; Burroughs, Lauri M; Bleesing, Jack; Kapoor, Neena; Dara, Jasmeen; Williams, Olatundun; Kapadia, Malika; Oshrine, Benjamin R; Bednarski, Jeffrey J; Rayes, Ahmad; Chong, Hey; Cuvelier, Geoffrey D E; Forbes Satter, Lisa R; Martinez, Caridad; Vander Lugt, Mark T; Yu, Lolie C; Chandrakasan, Shanmuganathan; Joshi, Avni; Prockop, Susan E; Dávila Saldaña, Blachy J; Aquino, Victor; Broglie, Larisa A; Ebens, Christen L; Madden, Lisa M; DeSantes, Kenneth; Milner, Jordan; Rangarajan, Hemalatha G; Shah, Ami J; Gillio, Alfred P; Knutsen, Alan P; Miller, Holly K; Moore, Theodore B; Graham, Pamela; Bauchat, Andrea; Bunin, Nancy J; Teira, Pierre; Petrovic, Aleksandra; Chandra, Sharat; Abdel-Azim, Hisham; Dorsey, Morna J; Birbrayer, Olga; Cowan, Morton J; Dvorak, Christopher C; Haddad, Elie; Kohn, Donald B; Notarangelo, Luigi D; Pai, Sung-Yun; Puck, Jennifer M; Pulsipher, Michael A; Torgerson, Troy R; Malech, Harry L; Kang, Elizabeth M

Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome

造血干细胞基因治疗Wiskott-Aldrich综合征的疗效

Labrosse, Roxane; Chu, Julia I; Armant, Myriam A; Everett, John K; Pellin, Danilo; Kareddy, Niharika; Frelinger, Andrew L; Henderson, Lauren A; O'Connell, Amy E; Biswas, Amlan; Coenen-van der Spek, Jet; Miggelbrink, Alexandra; Fiorini, Claudia; Adhikari, Hriju; Berry, Charles C; Cantu, Vito Adrian; Fong, Johnson; Jaroslavsky, Jason; Karadeniz, Derin F; Li, Quan-Zhen; Reddy, Shantan; Roche, Aoife M; Zhu, Chengsong; Whangbo, Jennifer S; Dansereau, Colleen; Mackinnon, Brenda; Morris, Emily; Koo, Stephanie M; London, Wendy B; Baris, Safa; Ozen, Ahmet; Karakoc-Aydiner, Elif; Despotovic, Jenny M; Forbes Satter, Lisa R; Saitoh, Akihiko; Aizawa, Yuta; King, Alejandra; Nguyen, Mai Anh Thi; Vu, Vy Do Uyen; Snapper, Scott B; Galy, Anne; Notarangelo, Luigi D; Bushman, Frederic D; Williams, David A; Pai, Sung-Yun

Interplay between epigenetic and genetic alterations in inborn errors of immunity

先天性免疫缺陷中表观遗传和遗传改变的相互作用

Rodríguez-Ubreva, Javier; Calvillo, Celia L; Forbes Satter, Lisa R; Ballestar, Esteban

Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

单基因早发性淋巴增殖和自身免疫:STAT3功能获得综合征的自然史

Leiding, Jennifer W; Vogel, Tiphanie P; Santarlas, Valentine G J; Mhaskar, Rahul; Smith, Madison R; Carisey, Alexandre; Vargas-Hernández, Alexander; Silva-Carmona, Manuel; Heeg, Maximilian; Rensing-Ehl, Anne; Neven, Bénédicte; Hadjadj, Jérôme; Hambleton, Sophie; Ronan Leahy, Timothy; Meesilpavikai, Kornvalee; Cunningham-Rundles, Charlotte; Dutmer, Cullen M; Sharapova, Svetlana O; Taskinen, Mervi; Chua, Ignatius; Hague, Rosie; Klemann, Christian; Kostyuchenko, Larysa; Morio, Tomohiro; Thatayatikom, Akaluck; Ozen, Ahmet; Scherbina, Anna; Bauer, Cindy S; Flanagan, Sarah E; Gambineri, Eleonora; Giovannini-Chami, Lisa; Heimall, Jennifer; Sullivan, Kathleen E; Allenspach, Eric; Romberg, Neil; Deane, Sean G; Prince, Benjamin T; Rose, Melissa J; Bohnsack, John; Mousallem, Talal; Jesudas, Rohith; Santos Vilela, Maria Marluce Dos; O'Sullivan, Michael; Pachlopnik Schmid, Jana; Průhová, Štěpánka; Klocperk, Adam; Rees, Matthew; Su, Helen; Bahna, Sami; Baris, Safa; Bartnikas, Lisa M; Chang Berger, Amy; Briggs, Tracy A; Brothers, Shannon; Bundy, Vanessa; Chan, Alice Y; Chandrakasan, Shanmuganathan; Christiansen, Mette; Cole, Theresa; Cook, Matthew C; Desai, Mukesh M; Fischer, Ute; Fulcher, David A; Gallo, Silvanna; Gauthier, Amelie; Gennery, Andrew R; Gonçalo Marques, José; Gottrand, Frédéric; Grimbacher, Bodo; Grunebaum, Eyal; Haapaniemi, Emma; Hämäläinen, Sari; Heiskanen, Kaarina; Heiskanen-Kosma, Tarja; Hoffman, Hal M; Gonzalez-Granado, Luis Ignacio; Guerrerio, Anthony L; Kainulainen, Leena; Kumar, Ashish; Lawrence, Monica G; Levin, Carina; Martelius, Timi; Neth, Olaf; Olbrich, Peter; Palma, Alejandro; Patel, Niraj C; Pozos, Tamara; Preece, Kahn; Lugo Reyes, Saúl Oswaldo; Russell, Mark A; Schejter, Yael; Seroogy, Christine; Sinclair, Jan; Skevofilax, Effie; Suan, Daniel; Suez, Daniel; Szabolcs, Paul; Velasco, Helena; Warnatz, Klaus; Walkovich, Kelly; Worth, Austen; Seppänen, Mikko R J; Torgerson, Troy R; Sogkas, Georgios; Ehl, Stephan; Tangye, Stuart G; Cooper, Megan A; Milner, Joshua D; Forbes Satter, Lisa R

Standardizing Anaphylaxis Treatment in Pediatric Care Settings

在儿科护理机构中规范过敏性休克治疗

Anvari, Sara; Szafron, Vibha; Hilliard, Tanya J; Forbes-Satter, Lisa; Shah, Mona D

Outcomes following treatment for ADA-deficient severe combined immunodeficiency: a report from the PIDTC

ADA缺陷型重症联合免疫缺陷治疗后的结局:来自PIDTC的报告

Cuvelier, Geoffrey D E; Logan, Brent R; Prockop, Susan E; Buckley, Rebecca H; Kuo, Caroline Y; Griffith, Linda M; Liu, Xuerong; Yip, Alison; Hershfield, Michael S; Ayoub, Paul G; Moore, Theodore B; Dorsey, Morna J; O'Reilly, Richard J; Kapoor, Neena; Pai, Sung-Yun; Kapadia, Malika; Ebens, Christen L; Forbes Satter, Lisa R; Burroughs, Lauri M; Petrovic, Aleksandra; Chellapandian, Deepak; Heimall, Jennifer; Shyr, David C; Rayes, Ahmad; Bednarski, Jeffrey J; Chandra, Sharat; Chandrakasan, Shanmuganathan; Gillio, Alfred P; Madden, Lisa; Quigg, Troy C; Caywood, Emi H; Dávila Saldaña, Blachy J; DeSantes, Kenneth; Eissa, Hesham; Goldman, Frederick D; Rozmus, Jacob; Shah, Ami J; Vander Lugt, Mark T; Thakar, Monica S; Parrott, Roberta E; Martinez, Caridad; Leiding, Jennifer W; Torgerson, Troy R; Pulsipher, Michael A; Notarangelo, Luigi D; Cowan, Morton J; Dvorak, Christopher C; Haddad, Elie; Puck, Jennifer M; Kohn, Donald B

An ELF4 hypomorphic variant results in NK cell deficiency

ELF4 亚等位基因变异导致 NK 细胞缺陷

Sandra Andrea Salinas, Emily M Mace, Matilde I Conte, Chun Shik Park, Yu Li, Joshua I Rosario-Sepulveda, Sanjana Mahapatra, Emily K Moore, Evelyn R Hernandez, Ivan K Chinn, Abigail E Reed, Barclay J Lee, Alexander Frumovitz, Richard A Gibbs, Jennifer E Posey, Lisa R Forbes Satter, Akaluck Thatayatik