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

Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies

ACTB 和 ACTG1 相关非肌肉肌动蛋白病中的分子基因型-表型相关性

Di Donato, Nataliya; Thom, Andrew; Rump, Andreas; Greve, Johannes N; Cadiñanos, Juan; Calabrò, Rocco Salvatore; Cathey, Sara; Chung, Brian; Cope, Heidi; Costales, Maria; Cuvertino, Sara; Dinkel, Philine; Erripi, Kalliopi; Fry, Andrew E; Garavelli, Livia; Hoffjan, Sabine; Janzarik, Wibke G; Kreimer, Insa; Mancini, Grazia; Marin-Reina, Purificacion; Meinhardt, Andrea; Niehaus, Indra; Pilz, Daniela; Ricca, Ivana; Simarro, Fernando Santos; Schrock, Evelin; Marquardt, Anja; Taft, Manuel H; Tezcan, Kamer; Thunström, Sofia; Verhagen, Judith; Verloes, Alain; Wollnik, Bernd; Krawitz, Peter; Hsieh, Tzung-Chien; Seifert, Michael; Heide, Michael; Lawrence, Catherine B; Roberts, Neil A; Manstein, Dietmar J; Woolf, Adrian S; Banka, Siddharth

Organ-specific features of human kidney lymphatics are disrupted in chronic transplant rejection.

慢性移植排斥反应会破坏人类肾脏淋巴系统的器官特异性特征

Jafree Daniyal J, Stewart Benjamin J, Price Karen L, Kolatsi-Joannou Maria, Laroche Camille, Mohidin Barian, Davis Benjamin, Mitchell Hannah, Russell Lauren G, Del Rey Lucía Marinas, Wang Chun Jing, Mason William J, Lee Byung Il, Heptinstall Lauren, Subramanian Ayshwarya, Pomeranz Gideon, Moulding Dale, Wilson Laura, Wickenden Tahmina, Malik Saif N, Holroyd Natalie, Walsh Claire L, Chandler Jennifer C, Cao Kevin X, Winyard Paul Jd, Woolf Adrian S, Busche Marc Aurel, Walker-Samuel Simon, Walker Lucy Sk, Crompton Tessa, Scambler Peter J, Motallebzadeh Reza, Clatworthy Menna R, Long David A

Correction: Tumor- and host-derived heparanase-2 (Hpa2) attenuates tumorigenicity: role of Hpa2 in macrophage polarization and BRD7 nuclear localization

更正:肿瘤和宿主来源的肝素酶-2 (Hpa2) 减弱肿瘤发生能力:Hpa2 在巨噬细胞极化和 BRD7 核定位中的作用

Soboh, Soaad; Vorontsova, Avital; Farhoud, Malik; Barash, Uri; Naroditsky, Inna; Gross-Cohen, Miriam; Weissmann, Marina; Nishioka, Yasuhiko; Woolf, Adrian S; Roberts, Neil A; Shaked, Yuval; Ilan, Neta; Vlodavsky, Israel

CNSC-72. ADRENERGIC NEURONS OF THE LOCUS COERULEUS PROMOTE DIFFUSE MIDLINE GLIOMA GROWTH

CNSC-72. 蓝斑肾上腺素能神经元促进弥漫性中线胶质瘤生长

Lopes, Filipa M; Grenier, Celine; Jarvis, Benjamin W; Al Mahdy, Sara; Lène-McKay, Adrian; Gurney, Alison M; Newman, William G; Waddington, Simon N; Woolf, Adrian S; Roberts, Neil A; Noreen, Zarish; Mondal, Tanmoy; Moghekar, Abhay; Nunlee‐Blnad, Gail; Ghosh, Somiranjan Ghosh; Szulzewsky, Frank; Arora, Sonali; Arakaki, Aleena; Sievers, Philipp; Bonnin, Damian Almiron; Paddison, Patrick; Sahm, Felix; Cimino, Patrick; Gujral, Taranjit; Holland, Eric; Mader, Marius; Rodrigues, Adrian; Chernikova, Sophia; Wong, Zheng Hao Samuel; Wang, Yuelong; Petritsch, Claudia; Wernig, Marius; Gephart, Melanie Hayden; Gloria Byun, Youkyeong; Kim, Yoon Seok; Gavish, Avishai; Barron, Tara; Andini, Nadya; Ivec, Alexis; Drexler, Richard; Su, Minhui; Woo, Pamelyn; Geraghty, Anna; Logan, Natalie; Deisseroth, Karl; Monje, Michelle

Haploinsufficiency of ABL1 is associated with dominant isolated omphalocele

ABL1单倍体不足与显性孤立性脐膨出相关。

Kolvenbach, Caroline M; Yilmaz, Öznur; Lopes, Filipa M; Kalanithy, Jeshurun C; Lemberg, Katharina; Sharma, Vineeta; Majmundar, Amar J; Geyer, Matthias; Woolf, Adrian S; Hildebrandt, Friedhelm; Odermatt, Benjamin; Reutter, Heiko

Microvascular aberrations found in human polycystic kidneys are an early feature in a Pkd1 mutant mouse model.

人类多囊肾中发现的微血管异常是 Pkd1 突变小鼠模型的早期特征

Jafree Daniyal J, Perera Charith, Ball Mary, Tolomeo Daniele, Pomeranz Gideon, Wilson Laura, Davis Benjamin, Mason William J, Funk Eva Maria, Kolatsi-Joannou Maria, Polschi Radu, Malik Saif, Stewart Benjamin J, Price Karen L, Mitchell Hannah, Motallebzadeh Reza, Muto Yoshiharu, Lees Robert, Needham Sarah, Moulding Dale, Chandler Jennie C, Nandanwar Sonal, Walsh Claire L, Winyard Paul J D, Scambler Peter J, Hägerling René, Clatworthy Menna R, Humphreys Benjamin D, Lythgoe Mark F, Walker-Samuel Simon, Woolf Adrian S, Long David A

Case Report: Prolonged survival in Schinzel-Giedion syndrome featuring megaureter and de novo SETBP1 mutation.

病例报告:伴有巨输尿管和新生 SETBP1 突变的 Schinzel-Giedion 综合征患者长期生存

Beaman Glenda M, Jarvis Benjamin W, Goyal Anju, Keene David J B, Cervellione Max, Lopes Filipa M, Metcalfe Kay A, Woolf Adrian S, Newman William G

Tumor- and host-derived heparanase-2 (Hpa2) attenuates tumorigenicity: role of Hpa2 in macrophage polarization and BRD7 nuclear localization

肿瘤和宿主来源的肝素酶-2 (Hpa2) 可减弱肿瘤发生:Hpa2 在巨噬细胞极化和 BRD7 核定位中的作用

Soboh, Soaad; Vorontsova, Avital; Farhoud, Malik; Barash, Uri; Naroditsky, Inna; Gross-Cohen, Miriam; Weissmann, Marina; Nishioka, Yasuhiko; Woolf, Adrian S; Roberts, Neil A; Shaked, Yuval; Ilan, Neta; Vlodavsky, Israel

Neurogenic Defects Occur in LRIG2-Associated Urinary Bladder Disease

LRIG2相关膀胱疾病中会出现神经源性缺陷

Grenier, Celine; Lopes, Filipa M; Cueto-González, Anna M; Rovira-Moreno, Eulàlia; Gander, Romy; Jarvis, Benjamin W; McCloskey, Karen D; Gurney, Alison M; Beaman, Glenda M; Newman, William G; Woolf, Adrian S; Roberts, Neil A

Predicting congenital renal tract malformation genes using machine learning

利用机器学习预测先天性肾脏畸形基因

Kabir, Mitra; Stuart, Helen M; Lopes, Filipa M; Fotiou, Elisavet; Keavney, Bernard; Doig, Andrew J; Woolf, Adrian S; Hentges, Kathryn E