Kronquist相关文献与解析，生知库 | 链接生命科学的每一步

Age-related loss of Notch3 underlies brain vascular contractility deficiencies, glymphatic dysfunction, and neurodegeneration in mice

小鼠脑血管收缩力缺陷、淋巴系统功能障碍和神经退行性变是由Notch3的年龄相关性缺失引起的。

Romay, Milagros C; Knutsen, Russell H; Ma, Feiyang; Mompeón, Ana; Hernandez, Gloria E; Salvador, Jocelynda; Mirkov, Snezana; Batra, Ayush; Sullivan, David P; Procissi, Daniele; Buchanan, Samuel; Kronquist, Elise; Ferrante, Elisa A; Muller, William A; Walshon, Jordain; Steffens, Alicia; McCortney, Kathleen; Horbinski, Craig; Tournier-Lasserve, Elisabeth; Sonabend, Adam M; Sorond, Farzaneh A; Wang, Michael M; Boehm, Manfred; Kozel, Beth A; Iruela-Arispe, M Luisa

Notch

Pyridoxamine treatment ameliorates large artery stiffening and cerebral artery endothelial dysfunction in old mice

吡哆胺治疗可改善老年小鼠大动脉硬化和脑动脉内皮功能障碍

期刊:Journal of Cerebral Blood Flow and Metabolism

影响因子:4.9

doi:10.1177/0271678X221130124

Emily H Reeve, Elise K Kronquist, Julia R Wolf, Byron Lee, Aleena Khurana, Hanson Pham, Abigail E Cullen, Jessica A Peterson, Antonio Meza, R Colton Bramwell, Laura Villasana, Daniel R Machin, Grant D Henson, Ashley E Walker

信号转导

发表日期：2023

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High pulse pressure impairs cerebral artery endothelial function in young, but not old, mice

高脉压会损害年轻小鼠（而非老年小鼠）的脑动脉内皮功能。

期刊:Experimental Gerontology

影响因子:4.3

doi:10.1016/j.exger.2023.112101

Winder, Nick R; Reeve, Emily H; Kronquist, Elise K; Khurana, Aleena; Lee, Byron; Nguyen, Thuan; Henson, Grant D; Walker, Ashley E

神经科学

发表日期：2023

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Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiency

编码兼职 H 蛋白的 GCSH 致病变异导致非酮症高甘氨酸血症和脂肪酸缺乏症

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddac246

Laura Arribas-Carreira, Cristina Dallabona, Michael A Swanson, Joseph Farris, Elsebet Østergaard, Konstantinos Tsiakas, Maja Hempel, Cecile Aquaviva-Bourdain, Stefanos Koutsoukos, Nicholas V Stence, Martina Magistrati, Elaine B Spector, Kathryn Kronquist, Mette Christensen, Helena G Karstensen, René

代谢

发表日期：2023

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Elastin Insufficiency Confers Proximal and Distal Pulmonary Vasculopathy in Mice, Partially Remedied by the K(ATP) Channel Opener Minoxidil: Considerations and Cautions for the Treatment of People With Williams-Beuren Syndrome

弹性蛋白不足可导致小鼠近端和远端肺血管病变，K(ATP)通道开放剂米诺地尔可部分缓解该病变：威廉姆斯-博伊伦综合征患者治疗的注意事项和注意事项

期刊:Frontiers in Cardiovascular Medicine

影响因子:2.9

doi:10.3389/fcvm.2022.886813

Knutsen, Russell H; Gober, Leah M; Kronquist, Elise K; Kaur, Maninder; Donahue, Danielle R; Springer, Danielle; Yu, Zu Xi; Chen, Marcus Y; Fu, Yi-Ping; Choobdar, Feri; Nguyen, My-Le; Osgood, Sharon; Freeman, Joy L; Raja, Neelam; Levin, Mark D; Kozel, Beth A

发表日期：2022

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Inhibition of NOX1 Mitigates Blood Pressure Increases in Elastin Insufficiency

抑制 NOX1 可减轻弹性蛋白不足引起的血压升高

期刊:Function

影响因子:

doi:10.1093/function/zqab015

Angela Troia, Russell H Knutsen, Carmen M Halabi, Daniela Malide, Zu Xi Yu, Amanda Wardlaw-Pickett, Elise K Kronquist, Kit Man Tsang, Attila Kovacs, Robert P Mecham, Beth A Kozel

信号转导

发表日期：2021

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Vascular Casting of Adult and Early Postnatal Mouse Lungs for Micro-CT Imaging

成年及早期出生后小鼠肺血管铸型制备及微型CT成像

期刊:Jove-Journal of Visualized Experiments

影响因子:1

doi:10.3791/61242

Knutsen, Russell H; Gober, Leah M; Sukinik, Joseph R; Donahue, Danielle R; Kronquist, Elise K; Levin, Mark D; McLean, Sean E; Kozel, Beth A

Mouse

发表日期：2020

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The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy

导致吡哆醇依赖性癫痫的ALDH7A1基因突变的基因型谱：一种常见的癫痫性脑病

期刊:Journal of Inherited Metabolic Disease

影响因子:3.8

doi:10.1002/jimd.12045

Coughlin, Curtis R 2nd; Swanson, Michael A; Spector, Elaine; Meeks, Naomi J L; Kronquist, Kathryn E; Aslamy, Mezhgan; Wempe, Michael F; van Karnebeek, Clara D M; Gospe, Sidney M Jr; Aziz, Verena G; Tsai, Becky P; Gao, Hanlin; Nagy, Peter L; Hyland, Keith; van Dooren, Silvy J M; Salomons, Gajja S; Van Hove, Johan L K

Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines

脆性X染色体综合征检测中三核苷酸重复序列的临床意义：美国医学遗传学学会指南的阐释

期刊:Genetics in Medicine

影响因子:6.2

doi:10.1097/GIM.0b013e31818b0c8a

Kronquist, Kathryn E; Sherman, Stephanie L; Spector, Elaine B

发表日期：2008

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Reoperation Rates and Risk Factors after Spinal Cord Stimulation Revision Surgery

脊髓刺激翻修手术后的再次手术率和风险因素

Age-related loss of Notch3 underlies brain vascular contractility deficiencies, glymphatic dysfunction, and neurodegeneration in mice

小鼠脑血管收缩力缺陷、淋巴系统功能障碍和神经退行性变是由Notch3的年龄相关性缺失引起的。

Pyridoxamine treatment ameliorates large artery stiffening and cerebral artery endothelial dysfunction in old mice

吡哆胺治疗可改善老年小鼠大动脉硬化和脑动脉内皮功能障碍

High pulse pressure impairs cerebral artery endothelial function in young, but not old, mice

高脉压会损害年轻小鼠（而非老年小鼠）的脑动脉内皮功能。

Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiency

编码兼职 H 蛋白的 GCSH 致病变异导致非酮症高甘氨酸血症和脂肪酸缺乏症

Elastin Insufficiency Confers Proximal and Distal Pulmonary Vasculopathy in Mice, Partially Remedied by the K(ATP) Channel Opener Minoxidil: Considerations and Cautions for the Treatment of People With Williams-Beuren Syndrome

弹性蛋白不足可导致小鼠近端和远端肺血管病变，K(ATP)通道开放剂米诺地尔可部分缓解该病变：威廉姆斯-博伊伦综合征患者治疗的注意事项和注意事项

Inhibition of NOX1 Mitigates Blood Pressure Increases in Elastin Insufficiency

抑制 NOX1 可减轻弹性蛋白不足引起的血压升高

Vascular Casting of Adult and Early Postnatal Mouse Lungs for Micro-CT Imaging

成年及早期出生后小鼠肺血管铸型制备及微型CT成像

The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy

导致吡哆醇依赖性癫痫的ALDH7A1基因突变的基因型谱：一种常见的癫痫性脑病

Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines

脆性X染色体综合征检测中三核苷酸重复序列的临床意义：美国医学遗传学学会指南的阐释