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

The prevalence of ENPP1 deficiency in humans with OPLL and the preclinical efficacy of ENPP1 enzyme therapy in OPLL mice.

ENPP1 缺乏症在患有 OPLL 的人类中的患病率以及 ENPP1 酶疗法在 OPLL 小鼠中的临床前疗效。

Srivastava Shivani, Kato Hajime, von Kroge Simon, Weise Keith, Stabach Paul, Lopez Sam G, O'Brien Kevin, Lester Ethan R, Kim Hana, Ishaq Tayyaba, Dammen-Brower Kris, Schinke Thorsten, Kimura Soichiro, Miyahara Junya, Doi Toru, Oshima Yasushi, Yarema Kevin J, Carpenter Thomas O, Sabbagh Yves, Tommasini Steven M, Ito Nobuaki, Oheim Ralf, Braddock Demetrios T

Therapeutic approaches for the treatment of genetic and acquired cardiovascular calcification

治疗遗传性和获得性心血管钙化的治疗方法

O'Brien, Kevin; Husson, Hervé; Sabbagh, Yves

Recombinant ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) decreases vascular calcification and prevents osteomalacia in a rat model of chronic kidney disease.

重组外核苷酸焦磷酸酶/磷酸二酯酶 1 (ENPP1) 可减少慢性肾病大鼠模型中的血管钙化并预防骨软化症

O'Brien Kevin, Laurion Lisa, Sullivan Caitlin, Howe Jennifer, Lynch Angela Malin, Cheng Zhiliang, Schrier Denis, Husson Hervé, Sabbagh Yves

Quantitative correlation of ENPP1 pathogenic variants with disease phenotype.

ENPP1致病变异与疾病表型的定量相关性

Ansh Anenya Jai, Stabach Paul R, Ciccone Carla, Cao Wenxiang, De La Cruz Enrique M, Sabbagh Yves, Carpenter Thomas O, Ferreira Carlos R, Braddock Demetrios T

ENPP1 enzyme replacement therapy improves ectopic calcification but does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia.

ENPP1 酶替代疗法可改善异位钙化,但不能挽救颅骨干骺端发育不良小鼠模型的骨骼表型

Reichenberger Ernst J, O'Brien Kevin, Hatori Ayano, Carpenter Thomas O, van de Wetering Koen, Flaman Lisa, Howe Jennifer, Ortiz Daniel, Sabbagh Yves, Chen I-Ping

A Reference Range for Plasma Levels of Inorganic Pyrophosphate in Children Using the ATP Sulfurylase Method

采用ATP硫酸化酶法测定儿童血浆无机焦磷酸盐水平的参考范围

Bernhard, Eva; Nitschke, Yvonne; Khursigara, Gus; Sabbagh, Yves; Wang, Yongbao; Rutsch, Frank

Novel PHEX gene locus-specific database: Comprehensive characterization of vast number of variants associated with X-linked hypophosphatemia (XLH)

新型PHEX基因位点特异性数据库:对大量与X连锁低磷血症(XLH)相关的变异进行全面表征

Sarafrazi, Soodabeh; Daugherty, Sean C; Miller, Nicole; Boada, Patrick; Carpenter, Thomas O; Chunn, Lauren; Dill, Kariena; Econs, Michael J; Eisenbeis, Scott; Imel, Erik A; Johnson, Britt; Kiel, Mark J; Krolczyk, Stan; Ramesan, Prameela; Truty, Rebecca; Sabbagh, Yves

Erythropoietin stimulates murine and human fibroblast growth factor-23, revealing novel roles for bone and bone marrow

红细胞生成素刺激小鼠和人类成纤维细胞生长因子-23,揭示骨骼和骨髓的新功能

Clinkenbeard, Erica L; Hanudel, Mark R; Stayrook, Keith R; Appaiah, Hitesh Nidumanda; Farrow, Emily G; Cass, Taryn A; Summers, Lelia J; Ip, Colin S; Hum, Julia M; Thomas, Joseph C; Ivan, Mircea; Richine, Briana M; Chan, Rebecca J; Clemens, Thomas L; Schipani, Ernestina; Sabbagh, Yves; Xu, Linlin; Srour, Edward F; Alvarez, Marta B; Kacena, Melissa A; Salusky, Isidro B; Ganz, Tomas; Nemeth, Elizabeta; White, Kenneth E

Role of TGF-β in a mouse model of high turnover renal osteodystrophy.

TGF-β在小鼠高转换肾性骨营养不良模型中的作用

Liu Shiguang, Song Wenping, Boulanger Joseph H, Tang Wen, Sabbagh Yves, Kelley Brian, Gotschall Russell, Ryan Susan, Phillips Lucy, Malley Katie, Cao Xiaohong, Xia Tai-He, Zhen Gehua, Cao Xu, Ling Hong, Dechow Paul C, Bellido Teresita M, Ledbetter Steven R, Schiavi Susan C

Npt2b deletion attenuates hyperphosphatemia associated with CKD

Npt2b 缺失可减轻与慢性肾脏病相关的高磷血症

Schiavi, Susan C; Tang, Wen; Bracken, Christina; O'Brien, Stephen P; Song, Wenping; Boulanger, Joseph; Ryan, Susan; Phillips, Lucy; Liu, Shiguang; Arbeeny, Cynthia; Ledbetter, Steven; Sabbagh, Yves