FLNB相关文献与解析，生知库 | 链接生命科学的每一步

Bladen, John C; Wang, Jun; Moosajee, Mariya; Rahman, Muhammad; Sangaralingam, Ajanthah; Gogna, Vijay K; Chelala, Claude; O'Toole, Edel A; Philpott, Michael P

肿瘤

FLNB

肿瘤免疫

Severe Osteoporosis in Larsen Syndrome-A Case Report of Bone Morphology and A Novel Filamin B (FLNB) Variant

Larsen综合征中的严重骨质疏松症——骨形态学和一种新型丝状蛋白B（FLNB）变异体的病例报告

期刊:Calcified Tissue International

影响因子:3.2

doi:10.1007/s00223-025-01436-z

Juul, Trine Maxel; Thomsen, Lisbeth Koch; Andreasen, Christina Møller; Ejersted, Charlotte; Folkestad, Lars; Brusgaard, Klaus; Hansen, Stinus; Thomsen, Jesper Skovhus; Andersen, Thomas Levin; Frederiksen, Anja Lisbeth

MTMR7 regulates human spermatogonial stem cells proliferation and migration via targeting FLNB

MTMR7 通过靶向 FLNB 调控人类精原干细胞的增殖和迁移

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0327669

Zhou, Nianchao; Wu, Tiantian; Yu, Yi; Gao, Wenxin; Jiang, Bing; Hu, Haoyue; Huang, Xiaoyan; Shen, Cong; Wu, Yibo; Gao, Tingting

Patient-informed CRISPR Screen Identifies FLNB as a Novel Congenital Heart Disease and Ciliopathy Gene

基于患者信息的 CRISPR 筛选鉴定出 FLNB 是一种新型先天性心脏病和纤毛病基因

期刊:

影响因子:

doi:10.1101/2025.10.14.682288

Arrigo, Angelo; Rao, Venkatraman; Ratan, Aakrosh; Kulkarni, Saurabh S

Disruption of FLNB leads to skeletal malformation by interfering with skeletal segmentation through the HOX gene

FLNB 破坏会通过 HOX 基因干扰骨骼分割，从而导致骨骼畸形

期刊:Bone Reports

影响因子:2.9

doi:10.1016/j.bonr.2024.101746

Qiming Xu, Lijia Cui, Yude Lin, Leigh-Anne Cui, Weibo Xia

FLNB

发表日期：2024

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MYLKFLNB and DOCK1LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway

MYLKFLNB 和 DOCK1LAMA2 基因间的相互作用与类风湿性关节炎在黏着斑通路中相关

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2024.1375036

Veyssiere, Maëva; Rodriguez Ordonez, Maria Del Pilar; Chalabi, Smahane; Michou, Laetitia; Cornelis, François; Boland, Anne; Olaso, Robert; Deleuze, Jean-François; Petit-Teixeira, Elisabeth; Chaudru, Valérie

Severe skeletal dysplasia caused by a novel FLNB gene mutation

由一种新的FLNB基因突变引起的严重骨骼发育不良

期刊:BMJ Case Reports

影响因子:0.5

doi:10.1136/bcr-2023-257998

Madan, Ichchha; Jackson, Frank; Sahni, Simran; Figueroa, Reinaldo

A Stop-gain Variant c.220C>T (p.(Gln74*)) in FLNB Segregates with Spondylocarpotarsal Synostosis Syndrome in a Consanguineous Family

在近亲婚配家族中，FLNB基因的终止密码子变异c.220C>T (p.(Gln74*))与脊椎腕跗骨融合综合征共分离。

期刊:Yale Journal of Biology and Medicine

影响因子:3.9

doi:10.59249/UTCP9818

Shahid, Hamna; Shakoor, Nazish; Bibi, Anisa; Qazi, Asma Saleem; Saeed, Rida Fatima; Nawaz, Aqeela; Malik, Sajid; Mumtaz, Sara

FLNB

发表日期：2023

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CORR Insights®: Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion

CORR Insights®：对特发性马蹄内翻足患者进行全外显子组测序，揭示了一种复发性丝状蛋白B（FLNB）缺失

期刊:Clinical Orthopaedics and Related Research

影响因子:4.4

doi:10.1097/CORR.0000000000002033

Patient-informed CRISPR screen identifies FLNB as a congenital heart disease and ciliopathy gene

基于患者信息的 CRISPR 筛选将 FLNB 鉴定为先天性心脏病和纤毛病基因。

GLI2 and FLNB Define Periocular Morphoeic Basal Cell Carcinoma

GLI2 和 FLNB 定义眼周硬皮病基底细胞癌

Severe Osteoporosis in Larsen Syndrome-A Case Report of Bone Morphology and A Novel Filamin B (FLNB) Variant

Larsen综合征中的严重骨质疏松症——骨形态学和一种新型丝状蛋白B（FLNB）变异体的病例报告

MTMR7 regulates human spermatogonial stem cells proliferation and migration via targeting FLNB

MTMR7 通过靶向 FLNB 调控人类精原干细胞的增殖和迁移

Patient-informed CRISPR Screen Identifies FLNB as a Novel Congenital Heart Disease and Ciliopathy Gene

基于患者信息的 CRISPR 筛选鉴定出 FLNB 是一种新型先天性心脏病和纤毛病基因

Disruption of FLNB leads to skeletal malformation by interfering with skeletal segmentation through the HOX gene

FLNB 破坏会通过 HOX 基因干扰骨骼分割，从而导致骨骼畸形

MYLKFLNB and DOCK1LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway

MYLKFLNB 和 DOCK1LAMA2 基因间的相互作用与类风湿性关节炎在黏着斑通路中相关

Severe skeletal dysplasia caused by a novel FLNB gene mutation

由一种新的FLNB基因突变引起的严重骨骼发育不良

A Stop-gain Variant c.220C>T (p.(Gln74*)) in FLNB Segregates with Spondylocarpotarsal Synostosis Syndrome in a Consanguineous Family

在近亲婚配家族中，FLNB基因的终止密码子变异c.220C>T (p.(Gln74*))与脊椎腕跗骨融合综合征共分离。

CORR Insights®: Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion

CORR Insights®：对特发性马蹄内翻足患者进行全外显子组测序，揭示了一种复发性丝状蛋白B（FLNB）缺失

Patient-informed CRISPR screen identifies FLNB as a congenital heart disease and ciliopathy gene

基于患者信息的 CRISPR 筛选将 FLNB 鉴定为先天性心脏病和纤毛病基因。

GLI2 and FLNB Define Periocular Morphoeic Basal Cell Carcinoma

GLI2 和 FLNB 定义眼周硬皮病基底细胞癌

Severe Osteoporosis in Larsen Syndrome-A Case Report of Bone Morphology and A Novel Filamin B (FLNB) Variant

Larsen综合征中的严重骨质疏松症——骨形态学和一种新型丝状蛋白B（FLNB）变异体的病例报告

MTMR7 regulates human spermatogonial stem cells proliferation and migration via targeting FLNB

MTMR7 通过靶向 FLNB 调控人类精原干细胞的增殖和迁移

Patient-informed CRISPR Screen Identifies FLNB as a Novel Congenital Heart Disease and Ciliopathy Gene

基于患者信息的 CRISPR 筛选鉴定出 FLNB 是一种新型先天性心脏病和纤毛病基因

Disruption of FLNB leads to skeletal malformation by interfering with skeletal segmentation through the HOX gene

FLNB 破坏会通过 HOX 基因干扰骨骼分割，从而导致骨骼畸形

MYLK*FLNB and DOCK1*LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway

MYLK*FLNB 和 DOCK1*LAMA2 基因间的相互作用与类风湿性关节炎在黏着斑通路中相关

Severe skeletal dysplasia caused by a novel FLNB gene mutation

由一种新的FLNB基因突变引起的严重骨骼发育不良

A Stop-gain Variant c.220C>T (p.(Gln74*)) in FLNB Segregates with Spondylocarpotarsal Synostosis Syndrome in a Consanguineous Family

在近亲婚配家族中，FLNB基因的终止密码子变异c.220C>T (p.(Gln74*))与脊椎腕跗骨融合综合征共分离。

CORR Insights®: Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion

CORR Insights®：对特发性马蹄内翻足患者进行全外显子组测序，揭示了一种复发性丝状蛋白B（FLNB）缺失

MYLKFLNB and DOCK1LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway

MYLKFLNB 和 DOCK1LAMA2 基因间的相互作用与类风湿性关节炎在黏着斑通路中相关