Dimori相关文献与解析，生知库 | 链接生命科学的每一步

Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta

I型胶原蛋白的独特改变会导致成骨不全小鼠模型出现不同程度的肺部和呼吸系统固有缺陷。

期刊:Journal of Physiology-London

影响因子:4.4

doi:10.1113/JP283452

Dimori, Milena; Fett, Jordan; Leikin, Sergey; Otsuru, Satoru; Thostenson, Jeff D; Carroll, John L; Morello, Roy

发表日期：2023

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A Rab33b missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylation

Smith-McCort 发育不良症的 Rab33b 错义小鼠模型显示骨吸收缺陷和蛋白质糖基化改变

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2023.1204296

Milena Dimori, Irina D Pokrovskaya, Shijie Liu, John T Sherrill, Horacio Gomez-Acevedo, Qiang Fu, Brian Storrie, Vladimir V Lupashin, Roy Morello

发育与干细胞

发表日期：2023

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Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass

分子伴侣介导的自噬丧失与椎骨松质骨量低有关

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-022-07157-9

Nisreen Akel, Ryan S MacLeod, Stuart B Berryhill, Dominique J Laster, Milena Dimori, Julie A Crawford, Qiang Fu, Melda Onal

Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers-Danlos syndrome.

Col5a1 单倍体不足会导致经典埃勒斯-当洛斯综合征小鼠模型出现内在的肺部和呼吸系统变化

期刊:Physiological Reports

影响因子:1.9

doi:10.14814/phy2.15275

Fett Jordan, Dimori Milena, Carroll John L, Morello Roy

Mouse

发表日期：2022

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Dental and craniofacial defects in the Crtap(-/-) mouse model of osteogenesis imperfecta type VII

第七型成骨不全症Crtap(-/-)小鼠模型中的牙齿和颅面缺陷

期刊:Developmental Dynamics

影响因子:1.5

doi:10.1002/dvdy.166

Xu, He; Lenhart, Sydney A; Chu, Emily Y; Chavez, Michael B; Wimer, Helen F; Dimori, Milena; Somerman, Martha J; Morello, Roy; Foster, Brian L; Hatch, Nan E

发表日期：2020

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The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis Imperfecta

成骨不全症小鼠模型中的骨细胞转录组广泛失调

期刊:JBMR Plus

影响因子:3.4

doi:10.1002/jbm4.10171

Sarah M Zimmerman, Milena Dimori, Melissa E Heard-Lipsmeyer, Roy Morello

Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim)

骨细胞中 RANKL 的缺失显著增加了成骨不全症小鼠的松质骨量 (oim)

期刊:Bone Reports

影响因子:2.9

doi:10.1016/j.bonr.2018.06.008

Sarah M Zimmerman, Melissa E Heard-Lipsmeyer, Milena Dimori, Jeff D Thostenson, Erin M Mannen, Charles A O'Brien, Roy Morello

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm

胶原修饰 Leprecan 蛋白在小鼠性腺组织和成熟精子中的表达特征和功能意义

期刊:AIMS Genetics

影响因子:

doi:10.3934/genet.2018.1.24

Sarah M Zimmerman, Roberta Besio, Melissa E Heard-Lipsmeyer, Milena Dimori, Patrizio Castagnola, Frances L Swain, Dana Gaddy, Alan B Diekman, Roy Morello

P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA

P3h3 缺陷和 Sc65 缺陷小鼠表型模拟 Ehlers-Danlos 综合征 VIA 型胶原赖氨酸羟基化不足和交联异常

期刊:Journal of Biological Chemistry

影响因子:4

doi:10.1074/jbc.M116.762245

David M Hudson, MaryAnn Weis, Jyoti Rai, Kyu Sang Joeng, Milena Dimori, Brendan H Lee, Roy Morello, David R Eyre

信号转导

发表日期：2017

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A new Col1a1 conditional knock-in mouse model to study osteogenesis imperfecta.

一种用于研究成骨不全症的新型 Col1a1 条件性敲入小鼠模型

Distinct type I collagen alterations cause intrinsic lung and respiratory defects of variable severity in mouse models of osteogenesis imperfecta

I型胶原蛋白的独特改变会导致成骨不全小鼠模型出现不同程度的肺部和呼吸系统固有缺陷。

A Rab33b missense mouse model for Smith-McCort dysplasia shows bone resorption defects and altered protein glycosylation

Smith-McCort 发育不良症的 Rab33b 错义小鼠模型显示骨吸收缺陷和蛋白质糖基化改变

Loss of chaperone-mediated autophagy is associated with low vertebral cancellous bone mass

分子伴侣介导的自噬丧失与椎骨松质骨量低有关

Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers-Danlos syndrome.

Col5a1 单倍体不足会导致经典埃勒斯-当洛斯综合征小鼠模型出现内在的肺部和呼吸系统变化

Dental and craniofacial defects in the Crtap(-/-) mouse model of osteogenesis imperfecta type VII

第七型成骨不全症Crtap(-/-)小鼠模型中的牙齿和颅面缺陷

The Osteocyte Transcriptome Is Extensively Dysregulated in Mouse Models of Osteogenesis Imperfecta

成骨不全症小鼠模型中的骨细胞转录组广泛失调

Loss of RANKL in osteocytes dramatically increases cancellous bone mass in the osteogenesis imperfecta mouse (oim)

骨细胞中 RANKL 的缺失显著增加了成骨不全症小鼠的松质骨量 (oim)

Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm

胶原修饰 Leprecan 蛋白在小鼠性腺组织和成熟精子中的表达特征和功能意义

P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA

P3h3 缺陷和 Sc65 缺陷小鼠表型模拟 Ehlers-Danlos 综合征 VIA 型胶原赖氨酸羟基化不足和交联异常