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

Intestinal interoceptive dysfunction drives age-associated cognitive decline

肠道内感受功能障碍是导致与年龄相关的认知衰退的原因。

Cox, Timothy O; Devason, Ashwarya S; de Araujo, Alan; Mason, Sydney; Subramanian, Madhav; Salvador, Andrea F M; Descamps, Hélène C; Kim, Junwon; Zhu, Yixuan; Litichevskiy, Lev; Jung, Sunhee; Song, Won-Suk; Cortés-Martín, Adrián; Henderson, Nathan T; Huang, Kuei-Pin; Nguyen, Thao; Sae-Lee, Wisath; Umana, Iboro C; Sacta, Maria; Rahman, Ryan J; Wisser, Stephen; Nelson, J Andrew D; Golynker, Ilona; McSween, Alana M; Hohmann, Eric F; Patel, Shaan; Bub, Anna L; Soekler, Clara; Blank, Niklas; Hoxha, Kevt'her; Boccia, Lavinia; Wong, Andrea C; Bahnsen, Klaas; Kim, Jihee; Biderman, Natalie; Abbasian, Dina; Shoffler, Clarissa; Petucci, Christopher; McAllister, Fiona E; Alhadeff, Amber L; Fuccillo, Marc V; Hill, Colin; Jang, Cholsoon; Betley, J Nicholas; de Lartigue, Guillaume; Lee, Virginia Y-M; Levy, Maayan; Thaiss, Christoph A

Detection of clinically relevant variants in the TP53 gene below 10% allelic frequency: A multicenter study by ERIC, the European Research Initiative on CLL

检测TP53基因中等位基因频率低于10%的临床相关变异:欧洲慢性淋巴细胞白血病研究计划(ERIC)的一项多中心研究

Pavlova, Sarka; Malcikova, Jitka; Radova, Lenka; Bonfiglio, Silvia; Cowland, Jack B; Brieghel, Christian; Andersen, Mette K; Karypidou, Maria; Biderman, Bella; Doubek, Michael; Lazarian, Gregory; Rapado, Inmaculada; Vynck, Matthijs; Porret, Naomi A; Andres, Martin; Rosenberg, Dina; Sahar, Dvora; Martínez-Laperche, Carolina; Buño, Ismael; Hindley, Andrew; Donaldson, David; Sánchez, Julio B; García-Marco, José A; Serrano-Alcalá, Alicia; Ferrer-Lores, Blanca; Fernández-Rodriguez, Concepción; Bellosillo, Beatriz; Stilgenbauer, Stephan; Tausch, Eugen; Nikdin, Hero; Quinn, Fiona; Atkinson, Emer; van de Corput, Lisette; Yildiz, Cafer; Bilbao-Sieyro, Cristina; Florido, Yanira; Thiede, Christian; Schuster, Caroline; Stoj, Anastazja; Czekalska, Sylwia; Chatzidimitriou, Anastasia; Laidou, Stamatia; Bidet, Audrey; Dussiau, Charles; Nollet, Friedel; Piras, Giovanna; Monne, Maria; Smirnova, Svetlana; Nikitin, Eugene; Sloma, Ivan; Claudel, Alexis; Largeaud, Laetitia; Ysebaert, Loïc; Valk, Peter J M; Christian, Amy; Walewska, Renata; Oscier, David; Sebastião, Marta; da Silva, Maria Gomes; Galieni, Piero; Angelini, Mario; Rossi, Davide; Spina, Valeria; Matos, Sónia; Martins, Vânia; Stokłosa, Tomasz; Pepek, Monika; Baliakas, Panagiotis; Andreu, Rafa; Luna, Irene; Kahre, Tiina; Murumets, Ülle; Pikousova, Tereza; Kurucova, Terezia; Laird, Sophie; Ward, Daniel; Alcoceba, Miguel; Balanzategui, Ana; Scarfo, Lydia; Gandini, Francesca; Zapparoli, Ettore; Blanco, Adoración; Abrisqueta, Pau; Rodríguez-Vicente, Ana E; Benito, Rocío; Bravetti, Clotilde; Davi, Frédéric; Gameiro, Paula; Martinez-Lopez, Joaquin; Tazón-Vega, Bárbara; Baran-Marszak, Fanny; Davis, Zadie; Catherwood, Mark; Sudarikov, Andrey; Rosenquist, Richard; Niemann, Carsten U; Stamatopoulos, Kostas; Ghia, Paolo; Pospisilova, Sarka

Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability

UBR5基因杂合变异会导致一种神经发育综合征,表现为发育迟缓、自闭症和智力障碍。

Sabeh, Pascale; Dumas, Samantha A; Maios, Claudia; Daghar, Hiba; Korzeniowski, Marek; Rousseau, Justine; Lines, Matthew; Guerin, Andrea; Millichap, John J; Landsverk, Megan; Grebe, Theresa; Lindstrom, Kristin; Strober, Jonathan; Ait Mouhoub, Tarik; Zweier, Christiane; Steinraths, Michelle; Hebebrand, Moritz; Callewaert, Bert; Abou Jamra, Rami; Kautza-Lucht, Monika; Wegler, Meret; Kruszka, Paul; Kumps, Candy; Banne, Ehud; Waberski, Marta Biderman; Dieux, Anne; Raible, Sarah; Krantz, Ian; Medne, Livija; Pechter, Kieran; Villard, Laurent; Guerrini, Renzo; Bianchini, Claudia; Barba, Carmen; Mei, Davide; Blanc, Xavier; Kallay, Christine; Ranza, Emmanuelle; Yang, Xiao-Ru; O'Heir, Emily; Donald, Kirsten A; Murugasen, Serini; Bruwer, Zandre; Calikoglu, Muge; Mathews, Jennifer M; Lesieur-Sebellin, Marion; Baujat, Geneviève; Derive, Nicolas; Pierson, Tyler Mark; Murrell, Jill R; Shillington, Amelle; Ormieres, Clothilde; Rondeau, Sophie; Reis, André; Fernandez-Jaen, Alberto; Au, Ping Yee Billie; Sweetser, David A; Briere, Lauren C; Couque, Nathalie; Perrin, Laurence; Schymick, Jennifer; Gueguen, Paul; Lefebvre, Mathilde; Van Andel, Michael; Juusola, Jane; Antonarakis, Stylianos E; Parker, J Alex; Burnett, Barrington G; Campeau, Philippe M

Missense Mutations in the KAT Domain of CREBBP Gene in Patients with Follicular Lymphoma: Implications for Differential Diagnosis and Prognosis

滤泡性淋巴瘤患者CREBBP基因KAT结构域错义突变:对鉴别诊断和预后的意义

Smolianinova, Anna; Bolshakov, Ivan; Sidorova, Yulia; Kovrigina, Alla; Obukhova, Tatiana; Gabeeva, Nelli; Gemdzhian, Eduard; Nikulina, Elena; Biderman, Bella; Severina, Nataliya; Risinskaya, Nataliya; Sudarikov, Andrey; Zvonkov, Eugeniy; Parovichnikova, Elena

Liquid Biopsy as a Means of Assessing Prognosis and Identifying Novel Risk Factors in Multiple Myeloma

液体活检作为评估多发性骨髓瘤预后和识别新型危险因素的一种手段

Soloveva, Maiia; Solovev, Maksim; Yakutik, Igor; Biderman, Bella; Nikulina, Elena; Risinskaya, Natalya; Obukhova, Tatiana; Gladysheva, Maria; Kovrigina, Alla; Chabaeva, Yulia; Kulikov, Sergei; Sudarikov, Andrey; Mendeleeva, Larisa

Prognostic impact of biomarkers in PMBCL: rationale for early integration of immune checkpoint inhibitors

生物标志物在原发性纵隔大B细胞淋巴瘤(PMBCL)预后中的作用:早期整合免疫检查点抑制剂的理论依据

Mangasarova, Yana K; Abdurashidova, Runiza R; Risinskaya, Natalya V; Biderman, Bella V; Abramova, Tatiana V; Surin, Vadim L; Shupletsova, Irina A; Obukhova, Tatiana N; Iusupov, Rasul I; Chabaeva, Yulia A; Magomedova, Aminat U; Nikulina, Lena E; Kulikov, Sergei M; Zvonkov, Eugene E; Kovrigina, Alla M; Sudarikov, Andrey B

Concerted actions of distinct serotonin neurons orchestrate female pup care behavior.

不同的血清素神经元协同作用,协调雌性幼崽的照护行为

Xiao Shuyun Alina, Chen Che Cherry, Horvath Patricia, Tsai Valerie, Cardenas Vibiana Marie, Biderman Dan, Deng Fei, Li Yulong, Linderman Scott W, Dulac Catherine, Luo Liqun

Concerted actions of distinct serotonin neurons orchestrate female pup care behavior.

不同的血清素神经元协同作用,协调雌性幼崽的照护行为

Xiao Shuyun Alina, Chen Che Cherry, Horvath Patricia, Tsai Valerie, Cardenas Vibiana Marie, Biderman Dan, Deng Fei, Li Yulong, Linderman Scott W, Dulac Catherine, Luo Liqun

Therapeutic strategies and treatment sequencing in patients with chronic lymphocytic leukemia: An international study of ERIC, the European Research Initiative on CLL

慢性淋巴细胞白血病患者的治疗策略和治疗顺序:欧洲慢性淋巴细胞白血病研究计划 (ERIC) 的一项国际研究

Chatzikonstantinou, Thomas; Scarfò, Lydia; Minga, Eva; Karakatsoulis, Georgios; Chamou, Dimitra; Kotaskova, Jana; Iacoboni, Gloria; Demosthenous, Christos; Albi, Elisa; Alcoceba, Miguel; Al-Shemari, Salem; Aurran-Schleinitz, Thérèse; Bacchiarri, Francesca; Chatzileontiadou, Sofia; Collado, Rosa; Davis, Zadie; de Deus Santos, Marcos Daniel; Dimou, Maria; Dmitrieva, Elena; Donaldson, David; Dos Santos, Gimena; Dreta, Barbara; Efstathopoulou, Maria; El-Ashwah, Shaimaa; Enrico, Alicia; Frygier, Andrzej; Galimberti, Sara; Galitzia, Andrea; Gimeno, Eva; Guarente, Valerio; Guieze, Romain; Harrop, Sean; Hatzimichael, Eleftheria; Herishanu, Yair; Hernández-Rivas, José-Ángel; Jaksic, Ozren; Kalicińska, Elżbieta; Laribi, Kamel; Karakus, Volkan; Kater, Arnon P; Kho, Bonnie; Kislova, Maria; Konstantinou, Εliana; Koren-Michowitz, Maya; Kotsianidis, Ioannis; Kubova, Zuzana; Labrador, Jorge; Lad, Deepesh; Laurenti, Luca; Longval, Thomas; Lopez-Garcia, Alberto; Marquet, Juan; Maslejova, Stanislava; Mayor-Bastida, Carlota; Mihaljevic, Biljana; Milosevic, Ivana; Miras, Fatima; Moia, Riccardo; Morawska, Marta; Nath, Uttam K; Navarro-Bailón, Almudena; Olivieri, Jacopo; Panovska-Stavridis, Irina; Papaioannou, Maria; Pierie, Cheyenne; Puiggros, Anna; Reda, Gianluigi; Rigolin, Gian M; Ruchlemer, Rosa; Schipani, Mattia; Schiwitza, Annett; Shen, Yandong; Shokralla, Tereza; Simkovic, Martin; Smirnova, Svetlana; Soliman, Dina S A; Stilgenbauer, Stephan; Tadmor, Tamar; Tomic, Kristina; Tse, Eric; Vassilakopoulos, Theodoros; Visentin, Andrea; Vitale, Candida; Vrachiolias, George; Vukovic, Vojin; Walewska, Renata; Xu, Zhenshu; Yagci, Munci; Yañez, Lucrecia; Yassin, Mohamed; Zuchnicka, Jana; Oscier, David; Gozzetti, Alessandro; Panagiotidis, Panagiotis; Bosch, Francesc; Sportoletti, Paolo; Espinet, Blanca; Pangalis, Gerassimos A; Popov, Viola M; Mulligan, Stephen; Angelopoulou, Maria; Demirkan, Fatih; Papajík, Tomas; Biderman, Bella; Murru, Roberta; Coscia, Marta; Tam, Constantine; Cuneo, Antonio; Gaidano, Gianluca; Claus, Rainer; Stavroyianni, Niki; Trentin, Livio; Antic, Darko; Smolej, Lukas; Kalashnikova, Olga B; Catherwood, Mark; Spacek, Martin; Pospisilova, Sarka; Doubek, Michael; Nikitin, Eugene; Chatzidimitriou, Anastasia; Ghia, Paolo; Stamatopoulos, Kostas

Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia

WDR83OS基因的纯合变异会导致伴有高胆汁酸血症的神经发育障碍。

Barish, Scott; Lin, Sheng-Jia; Maroofian, Reza; Gezdirici, Alper; Alhebby, Hamoud; Trimouille, Aurélien; Biderman Waberski, Marta; Mitani, Tadahiro; Huber, Ilka; Tveten, Kristian; Holla, Øystein L; Busk, Øyvind L; Houlden, Henry; Ghayoor Karimiani, Ehsan; Beiraghi Toosi, Mehran; Shervin Badv, Reza; Najarzadeh Torbati, Paria; Eghbal, Fatemeh; Akhondian, Javad; Al Safar, Ayat; Alswaid, Abdulrahman; Zifarelli, Giovanni; Bauer, Peter; Marafi, Dana; Fatih, Jawid M; Huang, Kevin; Petree, Cassidy; Calame, Daniel G; von der Lippe, Charlotte; Alkuraya, Fowzan S; Wali, Sami; Lupski, James R; Varshney, Gaurav K; Posey, Jennifer E; Pehlivan, Davut