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

DOCK8 in T cells promotes Th17 and Treg cell functionality to restrain mucosal mast cells and limit susceptibility to oral anaphylaxis

T细胞中的DOCK8促进Th17和Treg细胞的功能,从而抑制黏膜肥大细胞并降低对口服过敏反应的易感性。

Erin Janssen ,Mrinmoy Das ,Jordan Butts ,Mohammed Alasharee ,Saikat Mukherjee ,Gabriel L Lozano ,Chitong Rao ,Andrew F Livingston ,Brian Woods ,Emma Smith ,Zachary Peters ,Elena Milin ,Maria A Beamer ,Hazel Wilkie ,Juan-Manuel Leyva-Castillo ,Christy Kam ,Ali Sobh ,Majed Dasouki ,Rima Hanna Wakim ,Ghassan Dbaibo ,Waleed Al-Herz ,Talal A Chatila ,Fred D Finkelman ,Seth Rakoff-Nahoum ,Raif S Geha

CIROZ is dispensable in ancestral vertebrates but essential for left-right patterning in humans

CIROZ在脊椎动物祖先中并非必需,但对人类的左右模式形成至关重要。

Emmanuelle Szenker-Ravi ,Tim Ott ,Amirah Yusof ,Maya Chopra ,Muznah Khatoo ,Beatrice Pak ,Wei Xuan Goh ,Anja Beckers ,Angela F Brady ,Lisa J Ewans ,Nabila Djaziri ,Naif A M Almontashiri ,Malak Ali Alghamdi ,Essa Alharby ,Majed Dasouki ,Lindsay Romo ,Wen-Hann Tan ,Sateesh Maddirevula ,Fowzan S Alkuraya ,Jessica L Giordano ,Anna Alkelai ,Ronald J Wapner ,Karen Stals ,Majid Alfadhel ,Abdulrahman Faiz Alswaid ,Susanne Bogusch ,Anna Schafer-Kosulya ,Sebastian Vogel ,Philipp Vick ,Axel Schweickert ,Matthew Wakeling ,Anne Moreau de Bellaing ,Aisha M Alshamsi ,Damien Sanlaville ,Hamdi Mbarek ,Chadi Saad ,Sian Ellard ,Frank Eisenhaber ,Kornelia Tripolszki ,Christian Beetz ,Peter Bauer ,Achim Gossler ,Birgit Eisenhaber ,Martin Blum ,Patrice Bouvagnet ,Aida Bertoli-Avella ,Jeanne Amiel ,Christopher T Gordon ,Bruno Reversade

HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell Models.

HCN2 相关神经发育障碍:来自患者和非洲爪蟾细胞模型的数据

Houdayer Clara, Phillips A Marie, Chabbert Marie, Bourreau Jennifer, Maroofian Reza, Houlden Henry, Richards Kay, Saadi Nebal Waill, Dad'ová Eliška, Van Bogaert Patrick, Rupin Mailys, Keren Boris, Charles Perrine, Smol Thomas, Riquet Audrey, Pais Lynn, O'Donnell-Luria Anne, VanNoy Grace E, Bayat Allan, Møller Rikke S, Olofsson Kern, Jamra Rami Abou, Syrbe Steffen, Dasouki Majed, Seaver Laurie H, Sullivan Jennifer A, Shashi Vandana, Alkuraya Fowzan S, Poss Alexis F, Spence J Edward, Schnur Rhonda E, Forster Ian C, Mckenzie Chaseley E, Simons Cas, Wang Min, Snell Penny, Kothur Kavitha, Buckley Michael, Roscioli Tony, Elserafy Noha, Dauriat Benjamin, Procaccio Vincent, Henrion Daniel, Lenaers Guy, Colin Estelle, Verbeek Nienke E, Van Gassen Koen L, Legendre Claire, Bonneau Dominique, Reid Christopher A, Howell Katherine B, Ziegler Alban, Legros Christian

Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizures

干扰活动依赖性 CELF2 转运的基因变异会导致神经元过度兴奋、学习障碍和癫痫发作。

Hua, Michelle; Aghanoori, Mohamad-Reza; MacPherson, Melissa; Ren, Yi; Yang, Yifan; Or, Yan Yan; Williams, Laura; Gafuik, Christopher J; Quelin, Chloe; Keren, Boris; Schuhmann, Sarah; Vasileiou, Georgia; Bourgois, Alexia; Vitobello, Antonio; Philippe, Christophe; Stark, Zornitza; Leventer, Richard J; Tran-Mau-Them, Frederic; Tessarech, Marine; Prouteau, Clément; Lakeman, Phillis; Motazacker, Mahdi; Latner, Donald R; Caylor, Raymond; Prijoles, Eloise; Lichty, Angie; van Ierland, Yvette; Sweetser, David; Steel, Edward; Cobben, Jan; Dasouki, Majed J; Calame, Daniel; Wang, Gengyi; Rackel, Brooke; Ellis, James; He, Guiqiong; Mahoney, Douglas J; Innes, Micheil; Epp, Jonathan; Yang, Guang

Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome

扩大双糖链相关 Meester-Loeys 综合征的临床谱

Josephina A N Meester #, Anne Hebert #, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx, Kathryn Ashcroft, Paldeep S Atwal, Antoine Benichou, Clarisse Billon, Jan D Blankensteijn, Paul Brennan, Stephanie A Bucks, Ian M Campbell, Solène Conrad, Stephanie L Curtis, Majed Dasouki, Carolyn

Updates on the Surgical Approach to Fibroids: The Importance of Radiofrequency Ablation

子宫肌瘤外科治疗方法的最新进展:射频消融的重要性

Kwon, Caroline S; Abu-Alnadi, Noor Dasouki

A Non-Pharmacological Cough Therapy for People with Interstitial Lung Diseases: A Case Report

间质性肺病患者非药物止咳疗法:病例报告

Dasouki, Sabrina; Quach, Shirley; Mancopes, Renata; Mitchell, Sarah Chamberlain; Goldstein, Roger; Brooks, Dina; Oliveira, Ana

Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis

FOCAD 的缺失(通过 SKI 信使 RNA 监视通路发挥作用)会导致一种伴有肝硬化的儿童综合征。

Ricardo Moreno Traspas,Tze Shin Teoh,Pui-Mun Wong,Michael Maier,Crystal Y Chia,Kenneth Lay,Nur Ain Ali,Austin Larson,Fuad Al Mutairi,Nouriya Abbas Al-Sannaa,Eissa Ali Faqeih,Majid Alfadhel,Huma Arshad Cheema,Juliette Dupont,Stéphane Bézieau,Bertrand Isidor,Dorrain Yanwen Low,Yulan Wang,Grace Tan,Poh San Lai,Hugues Piloquet,Madeleine Joubert,Hulya Kayserili,Kimberly A Kripps,Shareef A Nahas,Eric P Wartchow,Mikako Warren,Gandham SriLakshmi Bhavani,Majed Dasouki,Renata Sandoval,Elisa Carvalho,Luiza Ramos,Gilda Porta,Bin Wu,Harsha Prasada Lashkari,Badr AlSaleem,Raeda M BaAbbad,Anabela Natália Abreu Ferrão,Vasiliki Karageorgou,Natalia Ordonez-Herrera,Suliman Khan,Peter Bauer,Benjamin Cogne,Aida M Bertoli-Avella,Marie Vincent,Katta Mohan Girisha,Bruno Reversade

Molecular classification of blood and bleeding disorder genes

血液和出血性疾病基因的分子分类

Baz, Batoul; Abouelhoda, Mohamed; Owaidah, Tarek; Dasouki, Majed; Monies, Dorota; Al Tassan, Nada

Comprehensive multi-omics analysis of G6PC3 deficiency-related congenital neutropenia with inflammatory bowel disease

对伴有炎症性肠病的G6PC3缺乏相关先天性中性粒细胞减少症进行全面的多组学分析

Dasouki, Majed; Alaiya, Ayodeele; ElAmin, Tanziel; Shinwari, Zakia; Monies, Dorota; Abouelhoda, Mohamed; Jabaan, Amjad; Almourfi, Feras; Rahbeeni, Zuhair; Alsohaibani, Fahad; Almohareb, Fahad; Al-Zahrani, Hazzaa; Guzmán Vega, Francisco J; Arold, Stefan T; Aljurf, Mahmoud; Ahmed, Syed Osman