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

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

Prophylactic PDE4 and PDE4B inhibition reduce lesion size and neutrophil infiltration following ischemic stroke in male mice

预防性抑制PDE4和PDE4B可减少雄性小鼠缺血性卒中后的病灶大小和中性粒细胞浸润。

Ponsaerts, Laura; Alders, Lotte; Schepers, Melissa; Kemps, Hannelore; Pirlet, Elke; Willems, Emily; De Bondt, Mirre; Jacobs, Ruben; Brullo, Chiara; Bruno, Olga; Fedele, Ernesto; Ricciarelli, Roberta; Prickaerts, Jos; Somers, Veerle; Vandenbosch, Michiel; Vanmierlo, Tim; Bronckaers, Annelies

The effect of sleep disturbances on the incidence of dementia for varying lag times

睡眠障碍对不同滞后时间痴呆症发病率的影响

Alders, Peter; Kok, Almar; van Zutphen, Elisabeth M; Claassen, Jurgen A H R; Deeg, Dorly J H

ARID2-related disorder: further delineation of the clinical phenotype of 27 novel individuals and description of an epigenetic signature

ARID2相关疾病:进一步阐明27例新患者的临床表型并描述其表观遗传特征

Houdayer, Clara; Rooney, Kathleen; van der Laan, Liselot; Bris, Céline; Alders, Mariëlle; Bahr, Angela; Barcia, Giulia; Battault, Clarisse; Begemann, Anais; Bonneau, Dominique; Bonnevalle, Antoine; Boughalem, Aicha; Bourges, Alice; Bournez, Marie; Bruel, Ange-Line; Buhas, Daniela; Carallis, Floriane; Cogné, Benjamin; Cormier-Daire, Valérie; Delanne, Julian; Demaret, Tanguy; Denommé-Pichon, Anne-Sophie; Désir, Julie; Dubourg, Christèle; Fradin, Mélanie; Geneviève, David; Goel, Himanshu; Goldenberg, Alice; Gripp, Karen W; Guichet, Agnès; Guimier, Anne; Jacquinet, Adeline; Keren, Boris; Legoff, Louis; Levy, Michael A; McConkey, Haley; Mendelsohn, Bryce A; Mignot, Cyril; Milon, Vincent; Nizon, Mathilde; Oneda, Beatrice; Pasquier, Laurent; Patat, Olivier; Philippe, Christophe; Procaccio, Vincent; Procopio, Rebecca; Prouteau, Clément; Rambaud, Thomas; Rauch, Anita; Relator, Raissa; Rondeau, Sophie; Santen, Gijs W E; Schleit, Jennifer; Sorlin, Arthur; Steindl, Katharina; Tedder, Matt; Tessarech, Marine; Mau-Them, Frédéric Tran; Trost, Detlef; Van der Sluijs, Pleuntje J; Vincent, Marie; Whalen, Sandra; Thauvin-Robinet, Christel; Isidor, Bertrand; Sadikovic, Bekim; Vitobello, Antonio; Colin, Estelle

The role of IGF-2 and its variants in enhancing endothelial migration and angiogenesis

IGF-2及其变体在促进内皮细胞迁移和血管生成中的作用

Lotte Alders ,Elke Pirlet ,Emma Gesquiere ,Annelies Bronckaers

Validation of a hypomorphic variant in CDK13 as the cause of CHDFIDD with autosomal recessive inheritance through determination of an episignature

通过确定表观遗传特征,验证 CDK13 中的低活性变异是常染色体隐性遗传 CHDFIDD 的病因

Fischer, Jan; Alders, Mariëlle; Mannens, Marcel M A M; Genevieve, David; Hackmann, Karl; Schröck, Evelin; Sadikovic, Bekim; Porrmann, Joseph

ImprintCap, a powerful NGS-based technology to investigate the molecular background of imprinting disorders

ImprintCap 是一种强大的基于新一代测序 (NGS) 的技术,用于研究印记障碍的分子背景。

Brioude, Frédéric; Haagmans, Martin A; Mannens, Marcel; Netchine, Irene; Alders, Marielle; Henneman, Peter; Bliek, Jet

CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature

CUL3相关神经发育障碍:20例新患者的临床表型及潜在表型相关表观遗传特征的鉴定

van der Laan, Liselot; Silva, Ananília; Kleinendorst, Lotte; Rooney, Kathleen; Haghshenas, Sadegheh; Lauffer, Peter; Alanay, Yasemin; Bhai, Pratibha; Brusco, Alfredo; de Munnik, Sonja; de Vries, Bert B A; Vega, Angelica Delgado; Engelen, Marc; Herkert, Johanna C; Hochstenbach, Ron; Hopman, Saskia; Kant, Sarina G; Kira, Ryutaro; Kato, Mitsuhiro; Keren, Boris; Kroes, Hester Y; Levy, Michael A; Lock-Hock, Ngu; Maas, Saskia M; Mancini, Grazia M S; Marcelis, Carlo; Matsumoto, Naomichi; Mizuguchi, Takeshi; Mussa, Alessandro; Mignot, Cyril; Närhi, Anu; Nordgren, Ann; Pfundt, Rolph; Polstra, Abeltje M; Trajkova, Slavica; van Bever, Yolande; José van den Boogaard, Marie; van der Smagt, Jasper J; Barakat, Tahsin Stefan; Alders, Mariëlle; Mannens, Marcel M A M; Sadikovic, Bekim; van Haelst, Mieke M; Henneman, Peter

Diversity, equity and inclusion in One Health could crucially support functional health security by fostering prevention, but a change in mindset is needed

在“同一健康”理念中,多样性、公平性和包容性对于通过促进预防来保障健康安全至关重要,但这需要转变观念。

Robbiati, Claudia; Andriamandroso, Antsa Miarisoa; Auerswald, Heidi; González, Mónica Berger; Becerra, Natalia Cediel; Dente, Maria Grazia; Dien, Nguyen Thi; Garnier, Julie; Onyango, Diana; Riley, Tamara; Weiszhar, Kim Laura; Winkler, Andrea Sylvia; Alders, Robyn

Nanopore sequencing enables combined detection of USP7 variants and a known Hao-Fountain syndrome episignature

纳米孔测序能够同时检测USP7变异体和已知的郝-方丹综合征表观遗传特征。

van der Laan, Liselot; Haagmans, Martin A; Venema, Andrea; Kerkhof, Jennifer; Levy, Michael A; Briuglia, Silvana; Caro, Pilar; Sailer, Sebastian; Schaaf, Christian P; Sadikovic, Bekim; van Haelst, Mieke M; van Gijn, Mariëlle; Alders, Mariëlle; Henneman, Peter