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

Normal Bone Matrix Mineralization but Altered Growth Plate Morphology in the Lmna(G609G/G609G) Mouse Model of Progeria

早衰症Lmna(G609G/G609G)小鼠模型中骨基质矿化正常,但生长板形态改变

Blouin, Stéphane; Hartmann, Markus A; Fratzl-Zelman, Nadja; Messmer, Phaedra; Whisenant, Daniel; Erdos, Michael R; Collins, Francis S; Eriksson, Maria; Strandgren, Charlotte; Cabral, Wayne A; Dechat, Thomas

Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model

纯合子G608G早衰小鼠模型颅面异常的特征分析

Beeram, Indeevar; Cubria, Maria Belen; Kamalapathy, Pramod; Yeritsyan, Diana; Dubose, Amanda J; Razavi, Ahmad Hedayatzadeh; Nafisi, Nazanin; Erdos, Michael R; Snyder, Brian D; Cabral, Wayne A; Collins, Francis S; Nazarian, Ara

Bone dysplasia in Hutchinson-Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations

哈钦森-吉尔福德早衰症中的骨发育不良与骨细胞群的分化和功能失调有关。

Cabral, Wayne A; Stephan, Chris; Terajima, Masahiko; Thaivalappil, Abhirami A; Blanchard, Owen; Tavarez, Urraca L; Narisu, Narisu; Yan, Tingfen; Wincovitch, Stephen M; Taga, Yuki; Yamauchi, Mitsuo; Kozloff, Kenneth M; Erdos, Michael R; Collins, Francis S

Genetic reduction of mTOR extends lifespan in a mouse model of Hutchinson-Gilford Progeria syndrome.

基因敲除 mTOR 可延长 Hutchinson-Gilford 早衰症小鼠模型的寿命

Cabral Wayne A, Tavarez Urraca L, Beeram Indeevar, Yeritsyan Diana, Boku Yoseph D, Eckhaus Michael A, Nazarian Ara, Erdos Michael R, Collins Francis S

Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups

以洛那法尼、普伐他汀和唑来膦酸为治疗组,评估G608G早衰症小鼠模型的肌肉骨骼表型

Cubria, Maria B; Suarez, Sebastian; Masoudi, Aidin; Oftadeh, Ramin; Kamalapathy, Pramod; DuBose, Amanda; Erdos, Michael R; Cabral, Wayne A; Karim, Lamya; Collins, Francis S; Snyder, Brian D; Nazarian, Ara

Melorheostotic Bone Lesions Caused by Somatic Mutations in MAP2K1 Have Deteriorated Microarchitecture and Periosteal Reaction

由MAP2K1体细胞突变引起的骨硬化性病变导致骨微结构和骨膜反应恶化

Fratzl-Zelman, Nadja; Roschger, Paul; Kang, Heeseog; Jha, Smita; Roschger, Andreas; Blouin, Stéphane; Deng, Zuoming; Cabral, Wayne A; Ivovic, Aleksandra; Katz, James; Siegel, Richard M; Klaushofer, Klaus; Fratzl, Peter; Bhattacharyya, Timothy; Marini, Joan C

Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect

TMEM38B基因突变引起的成骨不全症的表型谱:揭示复杂的细胞缺陷

Webb, Emma A; Balasubramanian, Meena; Fratzl-Zelman, Nadja; Cabral, Wayne A; Titheradge, Hannah; Alsaedi, Atif; Saraff, Vrinda; Vogt, Julie; Cole, Trevor; Stewart, Susan; Crabtree, Nicola J; Sargent, Brandi M; Gamsjaeger, Sonja; Paschalis, Eleftherios P; Roschger, Paul; Klaushofer, Klaus; Shaw, Nick J; Marini, Joan C; Högler, Wolfgang

Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expression

V 型成骨不全症原代成骨细胞尽管 COL1A1 表达降低,但仍表现出矿化作用增强。

Reich, Adi; Bae, Alison S; Barnes, Aileen M; Cabral, Wayne A; Hinek, Aleksander; Stimec, Jennifer; Hill, Suvimol C; Chitayat, David; Marini, Joan C

A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta

西非人中 1.5% 和非洲裔美国人中 0.4% 携带的 LEPRE1 基因创始突变会导致致命的隐性成骨不全症

Cabral, Wayne A; Barnes, Aileen M; Adeyemo, Adebowale; Cushing, Kelly; Chitayat, David; Porter, Forbes D; Panny, Susan R; Gulamali-Majid, Fizza; Tishkoff, Sarah A; Rebbeck, Timothy R; Gueye, Serigne M; Bailey-Wilson, Joan E; Brody, Lawrence C; Rotimi, Charles N; Marini, Joan C

Effects of tissue hydration on nanoscale structural morphology and mechanics of individual Type I collagen fibrils in the Brtl mouse model of Osteogenesis Imperfecta

组织水合作用对成骨不全症Brtl小鼠模型中I型胶原纤维纳米尺度结构形态和力学性能的影响

Kemp, Arika D; Harding, Chad C; Cabral, Wayne A; Marini, Joan C; Wallace, Joseph M