Matthew D Howell相关文献与解析，生知库 | 链接生命科学的每一步

Vagdevi Hangarakatte Ramachandra, Senthilkumar Sivanesan, Anand Koppal, Shanmugam Anandakumar, Matthew D Howell, Ethirajan Sukumar, Rajagopalan Vijayaraghavan

神经

帕金森

发表日期：2022

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Physical fitness in survivors of childhood Hodgkin lymphoma: A report from the St. Jude Lifetime Cohort

儿童霍奇金淋巴瘤幸存者的身体健康状况：来自圣裘德终生队列研究的报告

期刊:Pediatric Blood & Cancer

影响因子:2.3

doi:10.1002/pbc.27506

Wogksch, Matthew D; Howell, Carrie R; Wilson, Carmen L; Partin, Robyn E; Ehrhardt, Matthew J; Krull, Kevin R; Brinkman, Tara M; Mulrooney, Daniel A; Hudson, Melissa M; Robison, Leslie L; Ness, Kirsten K

淋巴瘤

发表日期：2019

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Activation of a cryptic 5' splice site reverses the impact of pathogenic splice site mutations in the spinal muscular atrophy gene

激活隐秘的 5' 剪接位点可逆转脊髓性肌萎缩症基因中致病剪接位点突变的影响

期刊:Nucleic Acids Research

影响因子:16.6

doi:10.1093/nar/gkx824

Natalia N Singh, José Bruno Del Rio-Malewski, Diou Luo, Eric W Ottesen, Matthew D Howell, Ravindra N Singh

Gender-Specific Amelioration of SMA Phenotype upon Disruption of a Deep Intronic Structure by an Oligonucleotide

寡核苷酸破坏深层内含子结构后 SMA 表型的性别特异性改善

期刊:Molecular Therapy

影响因子:12.1

doi:10.1016/j.ymthe.2017.03.036

Matthew D Howell, Eric W Ottesen, Natalia N Singh, Rachel L Anderson, Ravindra N Singh

TIA1 is a gender-specific disease modifier of a mild mouse model of spinal muscular atrophy

TIA1 是脊髓性肌萎缩症轻度小鼠模型的性别特异性疾病修饰因子

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-017-07468-2

Matthew D Howell, Eric W Ottesen, Natalia N Singh, Rachel L Anderson, Joonbae Seo, Senthilkumar Sivanesan, Elizabeth M Whitley, Ravindra N Singh

Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy

脊髓性肌萎缩症小鼠模型中 SMN 表达水平低，雄性生殖器官发育严重受损

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/srep20193

Eric W Ottesen, Matthew D Howell, Natalia N Singh, Joonbae Seo, Elizabeth M Whitley, Ravindra N Singh

Experimental evolution of an alternating uni- and multicellular life cycle in Chlamydomonas reinhardtii

莱茵衣藻单细胞和多细胞交替生活周期的实验演化

期刊:Nature Communications

影响因子:15.7

doi:10.1038/ncomms3742

Ratcliff, William C; Herron, Matthew D; Howell, Kathryn; Pentz, Jennifer T; Rosenzweig, Frank; Travisano, Michael

Selective decline of synaptic protein levels in the frontal cortex of female mice deficient in the extracellular metalloproteinase ADAMTS1

缺乏细胞外金属蛋白酶 ADAMTS1 的雌性小鼠额叶皮质突触蛋白水平选择性下降

期刊:PLoS One

影响因子:2.9

doi:10.1371/journal.pone.0047226

Matthew D Howell, Antoni X Torres-Collado, M Luisa Iruela-Arispe, Paul E Gottschall

Panel of synaptic protein ELISAs for evaluating neurological phenotype

用于评估神经表型的突触蛋白 ELISA 组

期刊:Experimental Brain Research

影响因子:1.7

doi:10.1007/s00221-010-2182-x

Paul E Gottschall, Joanne M Ajmo, Autumn K Eakin, Matthew D Howell, Hina Mehta, Lauren A Bailey

Embelin and levodopa combination therapy for improved Parkinson's disease treatment

恩贝林与左旋多巴联合治疗可改善帕金森病的治疗

Physical fitness in survivors of childhood Hodgkin lymphoma: A report from the St. Jude Lifetime Cohort

儿童霍奇金淋巴瘤幸存者的身体健康状况：来自圣裘德终生队列研究的报告

Activation of a cryptic 5' splice site reverses the impact of pathogenic splice site mutations in the spinal muscular atrophy gene

激活隐秘的 5' 剪接位点可逆转脊髓性肌萎缩症基因中致病剪接位点突变的影响

Gender-Specific Amelioration of SMA Phenotype upon Disruption of a Deep Intronic Structure by an Oligonucleotide

寡核苷酸破坏深层内含子结构后 SMA 表型的性别特异性改善

TIA1 is a gender-specific disease modifier of a mild mouse model of spinal muscular atrophy

TIA1 是脊髓性肌萎缩症轻度小鼠模型的性别特异性疾病修饰因子

Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy

脊髓性肌萎缩症小鼠模型中 SMN 表达水平低，雄性生殖器官发育严重受损

Experimental evolution of an alternating uni- and multicellular life cycle in Chlamydomonas reinhardtii

莱茵衣藻单细胞和多细胞交替生活周期的实验演化

Selective decline of synaptic protein levels in the frontal cortex of female mice deficient in the extracellular metalloproteinase ADAMTS1

缺乏细胞外金属蛋白酶 ADAMTS1 的雌性小鼠额叶皮质突触蛋白水平选择性下降

Panel of synaptic protein ELISAs for evaluating neurological phenotype

用于评估神经表型的突触蛋白 ELISA 组