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

The Paraoxonase (PON) Gene Family in Health, Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) and Other Diseases

对氧磷酶 (PON) 基因家族在健康、代谢功能障碍相关脂肪肝病 (MASLD) 和其他疾病中的作用

Huybrechts, Tammy; Franck, Kristien; Steenackers, Ellen; Van Hul, Wim

Gradual DNA methylation changes reveal transcription factors implicated in metabolic dysfunction-associated steatotic liver disease progression and epigenetic age acceleration

DNA甲基化的渐进性变化揭示了与代谢功能障碍相关的脂肪肝疾病进展和表观遗传年龄加速有关的转录因子。

Van Dijck, Evelien; Van Laere, Steven; Logie, Emilie; Timmermans, Steven; Fransen, Erik; Ibrahim, Joe; Kendall, Timothy J; Fallowfield, Jonathan A; Mateiu, Ligia M; Libert, Claude; Van Camp, Guy; Verrijken, An; Van Gaal, Luc; Francque, Sven; Van Hul, Wim; Berghe, Wim Vanden

Evolutionary and functional analyses of LRP5 in archaic and extant modern humans

对古人类和现代人类中LRP5的进化和功能分析

Roca-Ayats, Neus; Maceda, Iago; Bruque, Carlos David; Martínez-Gil, Núria; Garcia-Giralt, Natàlia; Cozar, Mónica; Mellibovsky, Leonardo; Van Hul, Wim; Lao, Oscar; Grinberg, Daniel; Balcells, Susanna

High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench

高骨量疾病:临床与基础研究相结合的新见解

Bergen, Dylan J M; Maurizi, Antonio; Formosa, Melissa M; McDonald, Georgina L K; El-Gazzar, Ahmed; Hassan, Neelam; Brandi, Maria-Luisa; Riancho, José A; Rivadeneira, Fernando; Ntzani, Evangelia; Duncan, Emma L; Gregson, Celia L; Kiel, Douglas P; Zillikens, M Carola; Sangiorgi, Luca; Högler, Wolfgang; Duran, Ivan; Mäkitie, Outi; Van Hul, Wim; Hendrickx, Gretl

Heterozygous pathogenic variants involving CBFB cause a new skeletal disorder resembling cleidocranial dysplasia

涉及 CBFB 的杂合致病变异会导致一种类似于锁骨颅骨发育不良的新型骨骼疾病。

Beyltjens, Tessi; Boudin, Eveline; Revencu, Nicole; Boeckx, Nele; Bertrand, Miriam; Schütz, Leon; Haack, Tobias B; Weber, Axel; Biliouri, Eleni; Vinkšel, Mateja; Zagožen, Anja; Peterlin, Borut; Pai, Shashidhar; Telegrafi, Aida; Henderson, Lindsay B; Ells, Courtney; Turner, Lesley; Wuyts, Wim; Van Hul, Wim; Hendrickx, Gretl; Mortier, Geert R

Identification of a Novel Nonsense Variant in the DLL3 Gene Underlying Spondylocostal Dysostosis in a Consanguineous Pakistani Family

在巴基斯坦近亲婚配家族中鉴定出DLL3基因中导致脊椎肋骨发育不全的新型无义变异

Khan, Feroz; Arshad, Abida; Ullah, Asmat; Steenackers, Ellen; Mortier, Geert; Ahmad, Wasim; Arshad, Muhammad; Khan, Sarmir; Hayat, Amir; Khan, Ikram; Khan, Muhammad Asim; Van Hul, Wim

Editorial: Innovative Models in Bone Biology: What can be Learned From Rare Bone Diseases?

社论:骨生物学创新模型:我们可以从罕见骨病中学到什么?

de Vries, Teun J; Van Hul, Wim; Eekhoff, E Marelise

Editorial: Innovative Therapies in Bone Biology: What Can Be Learned From Rare Bone Diseases?

社论:骨生物学创新疗法:我们可以从罕见骨病中学到什么?

Eekhoff, Elisabeth M W; de Vries, Teun J; Sakkers, Ralph J B; Van Hul, Wim

Rare Heterozygous PCSK1 Variants in Human Obesity: The Contribution of the p.Y181H Variant and a Literature Review.

人类肥胖中罕见的杂合 PCSK1 变异:p.Y181H 变异的贡献及文献综述

Van Dijck Evelien, Beckers Sigri, Diels Sara, Huybrechts Tammy, Verrijken An, Van Hoorenbeeck Kim, Verhulst Stijn, Massa Guy, Van Gaal Luc, Van Hul Wim

Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates

卡穆拉蒂-恩格尔曼病合并垂体功能减退:治疗挑战及双膦酸盐治疗结果的文献综述

Das, Liza; Dhiman, Vandana; Dutta, Pinaki; Sood, Ashwani; Prakash, Mahesh; Kaur, Simran; Steenackers, Ellen; Hendrickx, Gretl; Dayal, Devi; Van Hul, Wim; Bhadada, Sanjay Kumar