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

Lysosomal phosphoinositide turnover acts upstream of RagGTPase-mTORC1 and controls muscle growth.

溶酶体磷脂酰肌醇周转作用于 RagGTPase-mTORC1 的上游,并控制肌肉生长。

Picot Melanie, Hifdi Nesrine, Vaucourt Mathilde, Mansat Melanie, Li Peng, Singer Isabel, Chicanne Gaëtan, Stella Alexandre, Kuang Shen, Miceli Caterina, Henneman Nathaniel F, Payrastre Bernard, Vandromme Marie, Schiltz Odile, Nemazanyy Ivan, de Araujo Mariana E G, Panasyuk Ganna, Viaud Julien, Lämmerhofer Michael, Hnia Karim

Epigenome-wide analysis in West Africans identifies DNA methylation markers for circulating adiponectin

西非人群的全表观基因组分析鉴定出循环脂联素的DNA甲基化标记

Mungamba, Muhulo Muhau; Wijburg, Johanna; van der Linden, Eva L; Chilunga, Felix P; Doumatey, Ayo P; Bentley, Amy R; Hayfron-Benjamin, Charles F; Sewani-Rusike, Constance R; Nkeh-Chungag, Benedicta N; Ahima, Rexford S; Agyemang, Charles; Henneman, Peter; Adeyemo, Adebowale A; Rotimi, Charles N; Meeks, Karlijn A C

Undetected cases after implementation of first-trimester anomaly scan in low-risk population: insights from the IMITAS study

在低风险人群中实施妊娠早期畸形筛查后未发现的病例:来自 IMITAS 研究的启示

Bronsgeest, K; Lust, E E R; Zaaijer, S C E; Henneman, L; Crombag, N; Bilardo, C M; Galjaard, R-J H; Sikkel, E; Teunissen, A K K; Bekker, M N; Haak, M C

Engineering of induced pluripotent stem cells for the efficient development of non-alloreactive, hypoimmunogenic CD8αβ CAR-T cells.

对诱导多能干细胞进行工程改造,以高效开发非同种异体反应性、低免疫原性的 CD8αβ CAR-T 细胞。

Nianias Alexandros, Katsarou Afroditi, Prins Henk Jan, Shahrabi Aida, van Velzen Cindy, Henneman Linda, Ruiter Ruud, Mutis Tuna, Groen Richard, Themeli Maria

DNA methylation episignature for Smith-Magenis and Potocki-Lupski syndromes: a mirror perspective

Smith-Magenis综合征和Potocki-Lupski综合征的DNA甲基化表观遗传特征:镜像视角

van der Laan, Liselot; Karimi, Karim; Rooney, Kathleen; Alders, Mariëlle; Brusco, Alfredo; Lasa-Aranzasti, Amaia; Brunetti-Pierri, Nicola; Cueto-Gonzalez, Anna M; DuPont, Barbara R; Cappuccio, Gerarda; Dubourg, Christele; Everman, David; Gatinois, Vincent; Ganne, Benjamin; Genevieve, David; Ferrero, Giovanni Battista; Kempers, Marlies; Levy, Michael A; Niceta, Marcello; Novelli, Antonio; Orlando, Valeria; Odent, Sylvie; Patterson, Wesley G; Polstra, Abeltje M; Roscioli, Tony; Ruiz-Pallares, Nathalie; Sabbagh, Quentin; Trajkova, Slavica; Tartaglia, Marco; Tedder, Matthew A; Toutain, Annick; Koehler, Udo; Valenzuela, Irena; van Hagen, Johanna M; van der Kevie-Kersemaekers, Anne-Marie; Henneman, Peter; Mannens, Marcel M A M; Sadikovic, Bekim; van Haelst, Mieke M

Integrative epigenetic and transcriptomic profiling of whole blood and fibroblasts in Hao-Fountain syndrome

郝泉综合征全血和成纤维细胞的整合表观遗传学和转录组学分析

van der Laan, Liselot; Zwart, Rob; Venema, Andrea; Mul, Adri N; Haagmans, Martin A; Hulsbosch, Bart; Dyment, David; Valenzuela, Irene; Caro, Pilar; Sailer, Sebastian; Schaaf, Christian P; Sadikovic, Bekim; Mannens, Marcel M A M; van Haelst, Mieke M; Purushothama, Manasa Kalya; Henneman, Peter

Multi-omics investigation of thyroid development and dysfunction in down syndrome

唐氏综合征甲状腺发育和功能障碍的多组学研究

Lauffer, Peter; Zwaveling-Soonawala, Nitash; Li Yim, Andrew Y F; van der Laan, Liselot; van Zelderen-Bhola, Shama; Venema, Andrea M; Mul, Adri N; Bugiani, Marianna; Siteur-van Rijnstra, Esther; Gunst, Quinn D; van den Hoff, Maurice J B; de Bakker, Bernadette S; Boelen, Anita; Henneman, Peter; van Trotsenburg, A S Paul

Early versus late termination for fetal anomalies: Women's perspectives and psychological impact in a mixed methods study

因胎儿畸形而早期终止妊娠与晚期终止妊娠:一项混合方法研究中女性的观点和心理影响

Lust, Eline E R; Bronsgeest, Kim; Henneman, Lidewij; Crombag, Neeltje M T H; Bilardo, Caterina M; Galjaard, Robert-Jan H; Sikkel, Esther; Coumans, Audrey B C; Elvan-Taşpınar, Ayten; Galjaard, Sander; Go, Attie T J I; Manten, Gwendolyn T R; Pajkrt, Eva; van Leeuwen, Elisabeth; Haak, Monique C; Bekker, Mireille N

Preferences of Pregnant Women and Healthcare Professionals on First-Trimester Ultrasound Screening for Fetal Anomalies: A Discrete Choice Experiment

孕妇和医护人员对妊娠早期胎儿畸形超声筛查的偏好:一项离散选择实验

Lust, Eline E R; Bronsgeest, Kim; Smith, Ian; Henneman, Lidewij; Crombag, Neeltje M T H; Bilardo, Caterina M; Galjaard, Robert-Jan H; Sikkel, Esther; Bekker, Mireille N; Haak, Monique C

DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects

NOTCH1 变异体的 DNA 甲基化分析揭示了非综合征型先天性心脏缺陷的首个表观遗传特征

Dombrowsky, Gregor; van der Laan, Liselot; Silva, Ananília; Breckpot, Jeroen; Audain, Enrique; Wilsdon, Anna; Levy, Michael A; Vos, Niels; Mannens, Marcel; Wang, Jiao; Jain, Anjali; Lesurf, Robert; Winlaw, David; Bezzina, Connie R; Thomas, Mary Ann; Caliebe, Almuth; Klaassen, Sabine; Berger, Felix; Dittrich, Sven; Stiller, Brigitte; Abdul-Khaliq, Hashim; Dähnert, Ingo; Bu'Lock, Frances; Loughna, Siobhan; Brook, J David; Mital, Seema; Russell, Robert B; Pickardt, Thomas; Bauer, Ulrike; Kramer, Hans-Heiner; Uebing, Anselm; Henneman, Peter; Sadikovic, Bekim; Postma, Alex; Hitz, Marc-Phillip