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

Disruption of the human cystin-1 myristoyl-electrostatic switch causes polycystic kidney disease that phenocopies autosomal recessive polycystic kidney disease

人类胱氨酸-1肉豆蔻酰静电开关的破坏会导致多囊肾病,其表型与常染色体隐性多囊肾病相似。

Yang, Chaozhe; Harafuji, Naoe; Watts, Jacob A; Tao, Binli; Moran, Claire; Clements, Jenna; Price, Kalyn; Laucevicius, Anthony; Burrill, Natalie; Gebb, Juliana; Soni, Shelly; Oliver, Edward; Savla, Jill J; Christ, Lori; Moldenhauer, Julie; Hartung, Erum A; Didier, Ryne; Santani, Avni; Sandford, Richard N; Selkirk, Lisa; Radley, Jessica A; Mann, Kathy; Simonicova, Ingrid; Karl, Rudolfo; Kariat Ashraf, Arsila Palliyulla; Wachten, Dagmar; Wilson, Landon; Bebok, Zsuzsanna; Caldovic, Ljubica; Guay-Woodford, Lisa M

Distribution of capsule and O types in Klebsiella pneumoniae causing neonatal sepsis in Africa and South Asia: A meta-analysis of genome-predicted serotype prevalence to inform potential vaccine coverage

非洲和南亚新生儿败血症致病肺炎克雷伯菌荚膜和O型分布:基于基因组预测血清型流行率的荟萃分析,旨在为潜在疫苗覆盖率提供信息

Stanton, Thomas D; Keegan, Shaun P; Abdulahi, Jabir A; Amulele, Anne V; Bates, Matthew; Heinz, Eva; Hooda, Yogesh; Hu, Weiming; Jain, Kajal; Kanwar, Samiah; Magobo, Rindidzani; Olwagen, Courtney P; Tembo, John M; Sonda, Tolbert; Strysko, Jonathan; Tigoi, Caroline C; Amin, Sameen Ahmad; Bittinger, Kyle; Cornick, Jennifer; Foster-Nyarko, Ebenezer; Gumbi, Wilson; Hotwani, Aneeta; Iqbal, Naveed; Jones, Steven M; Kabir, Furqan; Khan, Waqasuddin; Musyani, Chileshe L; McGann, Carolyn M; Mittal, Varsha; Moustafa, Ahmed M; Musicha, Patrick; Mwansa, James C L; Ndumba, Moreka L; Odih, Erkison E; Omuoyo, Donwilliams O; Pearse, Oliver; Phillips, Laura T; Planet, Paul J; Rasool, Aniqa Abdul; Rodrigues, Charlene M C; Sands, Kirsty; Tanmoy, Arif M; Theiller, Erin; Zuza, Allan M; Basu, Sulagna; Chan, Grace J; Iregbu, Kenneth C; Mazarati, Jean-Baptiste; Alemayehu, Semaria Solomon; Walsh, Timothy R; Zahra, Rabaab; Dramowski, Angela; Fwoloshi, Sombo; Labi, Appiah-Korang; Madrid, Lola; Obeng-Nkrumah, Noah; Ojok, David; Wadugu, Boaz D; Whitelaw, Andrew C; Bethou, Adhisivam; Bhargava, Anudita; Jindal, Atul; Nanavati, Ruchi N; Prasad, Priyanka S; Sastry, Apurba; Farooqi, Joveria Q; Ghanchi, Najia; Jehan, Fyezah; Khan, Erum; Agarwal, Ramesh K; Aiken, Alexander M; Berkley, James A; Coffin, Susan E; Feasey, Nicholas A; Govender, Nelesh P; Hamer, Davidson H; Madhi, Shabir A; Nisar, Muhammad Imran; Saha, Samir K; Saha, Senjuti; Sankar, Mari Jeeva; Wyres, Kelly L; Holt, Kathryn E

Safety and Efficacy of Obinutuzumab in Treating Lupus Nephritis: A Systematic Review

奥妥珠单抗治疗狼疮性肾炎的安全性和有效性:系统评价

Arif, Zainab; Ali, Hafsa; Siddiqui, Erum; Naeem, Shorrem; Amin, Mohammed Hammad Jaber

Progress, challenges, and pragmatic concessions in predicting relative risk of kidney survival in ARPKD

在预测ARPKD患者肾脏存活率相对风险方面取得的进展、面临的挑战和务实的妥协

Ng, Derek K; Matheson, Matthew B; Hartung, Erum A

Polycystic Kidney Disease in Children: The Current Status and the Next Horizon

儿童多囊肾病:现状与展望

Cadnapaphornchai, Melissa A; Dell, Katherine M; Gimpel, Charlotte; Guay-Woodford, Lisa M; Gulati, Ashima; Hartung, Erum A; Liebau, Max C; Mallett, Andrew J; Marlais, Matko; Mekahli, Djalila; Piccirilli, Alixandra; Seeman, Tomas; Tindal, Kristin; Winyard, Paul J D

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

TRMT1基因的双等位致病变异会破坏tRNA修饰并诱发神经发育障碍。

Efthymiou, Stephanie; Leo, Cailyn P; Deng, Chenghong; Lin, Sheng-Jia; Maroofian, Reza; Lin, Renee; Karagoz, Irem; Zhang, Kejia; Kaiyrzhanov, Rauan; Scardamaglia, Annarita; Owrang, Daniel; Turchetti, Valentina; Jahnke, Friederike; Huang, Kevin; Petree, Cassidy; Derrick, Anna V; Rees, Mark I; Alvi, Javeria Raza; Sultan, Tipu; Li, Chumei; Jacquemont, Marie-Line; Tran-Mau-Them, Frederic; Valenzuela-Palafoll, Maria; Sidlow, Rich; Yoon, Grace; Morrow, Michelle M; Carere, Deanna Alexis; O'Connor, Mary; Fleischer, Julie; Gerkes, Erica H; Phornphutkul, Chanika; Isidor, Bertrand; Rivier-Ringenbach, Clotilde; Philippe, Christophe; Kurul, Semra Hiz; Soydemir, Didem; Kara, Bulent; Sunnetci-Akkoyunlu, Deniz; Bothe, Viktoria; Platzer, Konrad; Wieczorek, Dagmar; Koch-Hogrebe, Margarete; Rahner, Nils; Thuresson, Ann-Charlotte; Matsson, Hans; Frykholm, Carina; Bozdoğan, Sevcan Tuğ; Bisgin, Atil; Chatron, Nicolas; Lesca, Gaetan; Cabet, Sara; Tümer, Zeynep; Hjortshøj, Tina D; Rønde, Gitte; Marquardt, Thorsten; Reunert, Janine; Afzal, Erum; Zamani, Mina; Azizimalamiri, Reza; Galehdari, Hamid; Nourbakhsh, Pardis; Chamanrou, Niloofar; Chung, Seo-Kyung; Suri, Mohnish; Benke, Paul J; Zaki, Maha S; Gleeson, Joseph G; Calame, Daniel G; Pehlivan, Davut; Yilmaz, Halil I; Gezdirici, Alper; Rad, Aboulfazl; Abumansour, Iman Sabri; Oprea, Gabriela; Bereketoğlu, Muhammed Burak; Banneau, Guillaume; Julia, Sophie; Zeighami, Jawaher; Ashoori, Saeed; Shariati, Gholamreza; Sedaghat, Alireza; Sabri, Alihossein; Hamid, Mohammad; Parvas, Sahere; Tajudin, Tajul Arifin; Abdullah, Uzma; Baig, Shahid Mahmood; Chung, Wendy K; Glazunova, Olga O; Sabine, Sigaudy; Cheema, Huma Arshad; Zifarelli, Giovanni; Bauer, Peter; Sidpra, Jai; Mankad, Kshitij; Vona, Barbara; Fry, Andrew E; Varshney, Gaurav K; Houlden, Henry; Fu, Dragony

Bi-allelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency

MRPL49基因的双等位基因变异会导致不同的临床表现,包括感觉神经性听力损失、脑白质营养不良和卵巢功能不全。

Thomas, Huw B; Demain, Leigh A M; Cabrera-Orefice, Alfredo; Schrauwen, Isabelle; Shamseldin, Hanan E; Rea, Alessandro; Bharadwaj, Thashi; Smith, Thomas B; Oláhová, Monika; Thompson, Kyle; He, Langping; Kaur, Namanpreet; Shukla, Anju; Abukhalid, Musaad; Ansar, Muhammad; Rehman, Sakina; Riazuddin, Saima; Abdulwahab, Firdous; Smith, Janine M; Stark, Zornitza; Mancilar, Hanifenur; Tumer, Sait; Esen, Fatma N; Uctepe, Eyyup; Topcu, Vehap; Yesilyurt, Ahmet; Afzal, Erum; Salari, Mehri; Carroll, Christopher; Zifarelli, Giovanni; Bauer, Peter; Kor, Deniz; Bulut, Fatma D; Houlden, Henry; Maroofian, Reza; Carrera, Samantha; Yue, Wyatt W; Munro, Kevin J; Alkuraya, Fowzan S; Jamieson, Peter; Ahmed, Zubair M; Leal, Suzanne M; Taylor, Robert W; Wittig, Ilka; O'Keefe, Raymond T; Newman, William G

Neurobiological Mechanisms Underlying Psychological Dysfunction After Brain Injuries

脑损伤后心理功能障碍的神经生物学机制

Unadkat, Prashin; Rebeiz, Tania; Ajmal, Erum; De Souza, Vincent; Xia, Angela; Jinu, Julia; Powell, Keren; Li, Chunyan

Structural and functional analysis of Pseudomonas aeruginosa PelA provides insight into the modification of the Pel exopolysaccharide

对铜绿假单胞菌 PelA 的结构和功能分析揭示了 Pel 胞外多糖的修饰机制。

Jaime C Van Loon ,François Le Mauff ,Mario A Vargas ,Stephanie Gilbert ,Roland Pfoh ,Zachary A Morrison ,Erum Razvi ,Mark Nitz ,Donald C Sheppard ,P Lynne Howell

miRNA biomarkers for prognosis and therapy monitoring in a multi-ethnic cohort with SARS-CoV-2 infection

miRNA生物标志物在SARS-CoV-2感染的多民族队列中的预后和治疗监测应用

Mustafa, Farah; Ahmad, Waqar; Gull, Bushra; Baby, Jasmin; Panicker, Neena G; Khader, Thanumol Abdul; Baki, Hala Abdul; Rehman, Erum; Salim, Asif M; Ahmed, Rubina L G; Khansaheb, Hamda H; Habous, Maya; AlDabal, Laila M J A; Jaballah, Soumeya; Alqassim, Saif S; Alsheikh-Ali, Alawi; Rizvi, Tahir A