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Results 1 - 10 of 91  for Great Falls College MSU

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1
The burden of trisomy 21 disrupts the proteostasis network in Down syndrome
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The burden of trisomy 21 disrupts the proteostasis network in Down syndrome

Aivazidis, Stefanos ; Coughlan, Christina M ; Rauniyar, Abhishek K ; Jiang, Hua ; Liggett, L. Alexander ; Maclean, Kenneth N ; Roede, James R Brodsky, Jeffrey L

PloS one, 2017, Vol.12 (4), p.e0176307 [Peer Reviewed Journal]

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2
Methylene-tetrahydrofolate reductase contributes to allergic airway disease
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Methylene-tetrahydrofolate reductase contributes to allergic airway disease

Eyring, Kenneth R ; Pedersen, Brent S ; Maclean, Kenneth N ; Stabler, Sally P ; Yang, Ivana V ; Schwartz, David A Tost, Jorg

PloS one, 2018, Vol.13 (1), p.e0190916 [Peer Reviewed Journal]

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3
Experimental evidence for therapeutic potential of taurine in the treatment of nonalcoholic fatty liver disease
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Experimental evidence for therapeutic potential of taurine in the treatment of nonalcoholic fatty liver disease

Gentile, Christopher L ; Nivala, Angela M ; Gonzales, Jon C ; Pfaffenbach, Kyle T ; Wang, Dong ; Wei, Yuren ; Jiang, Hua ; Orlicky, David J ; Petersen, Dennis R ; Pagliassotti, Michael J ; Maclean, Kenneth N

American journal of physiology. Regulatory, integrative and comparative physiology, 2011-12, Vol.301 (6), p.R1710-R1722 [Peer Reviewed Journal]

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4
GDF10 blocks hepatic PPARγ activation to protect against diet-induced liver injury
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GDF10 blocks hepatic PPARγ activation to protect against diet-induced liver injury

Platko, Khrystyna ; Lebeau, Paul F ; Byun, Jae Hyun ; Poon, Samantha V ; Day, Emily A ; MacDonald, Melissa E ; Holzapfel, Nicholas ; Mejia-Benitez, Aurora ; Maclean, Kenneth N ; Krepinsky, Joan C ; Austin, Richard C

Molecular metabolism (Germany), 2019-09, Vol.27, p.62-74 [Peer Reviewed Journal]

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5
Effects of neonatal neural progenitor cell implantation on adult neuroanatomy and cognition in the Ts65Dn model of Down syndrome
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Effects of neonatal neural progenitor cell implantation on adult neuroanatomy and cognition in the Ts65Dn model of Down syndrome

Rachubinski, Angela L ; Crowley, Shannon K ; Sladek, Jr, John R ; Maclean, Kenneth N ; Bjugstad, Kimberly B Gilestro, Giorgio F

PloS one, 2012, Vol.7 (4), p.e36082 [Peer Reviewed Journal]

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6
A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype
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A de novo 2.78-Mb duplication on chromosome 21q22.11 implicates candidate genes in the partial trisomy 21 phenotype

Weisfeld-Adams, James D ; Tkachuk, Amanda K ; Maclean, Kenneth N ; Meeks, Naomi L ; Scott, Stuart A

Npj genomic medicine, 2016, Vol.1 (1), p.16003 [Peer Reviewed Journal]

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7
Liver-Specific Deletion of Phosphatase and Tensin Homolog Deleted on Chromosome 10 Significantly Ameliorates Chronic EtOH-Induced Increases in Hepatocellular Damage
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Liver-Specific Deletion of Phosphatase and Tensin Homolog Deleted on Chromosome 10 Significantly Ameliorates Chronic EtOH-Induced Increases in Hepatocellular Damage

Shearn, Colin T ; Orlicky, David J ; McCullough, Rebecca L ; Jiang, Hua ; Maclean, Kenneth N ; Mercer, Kelly E ; Stiles, Bangyan L ; Saba, Laura M ; Ronis, Martin J ; Petersen, Dennis R Guillou, Hervé

PloS one, 2016, Vol.11 (4), p.e0154152

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8
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease
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Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease

Friederich, Marisa W ; Elias, Abdallah F ; Kuster, Alice ; Laugwitz, Lucia ; Larson, Austin A ; Landry, Aaron P ; Ellwood‐Digel, Logan ; Mirsky, David M ; Dimmock, David ; Haven, Jaclyn ; Jiang, Hua ; MacLean, Kenneth N ; Styren, Katie ; Schoof, Jonathan ; Goujon, Louise ; Lefrancois, Thomas ; Friederich, Maike ; Coughlin, Curtis R ; Banerjee, Ruma ; Haack, Tobias B ; Van Hove, Johan L. K

Journal of inherited metabolic disease, 2020-09, Vol.43 (5), p.1024-1036 [Peer Reviewed Journal]

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9
Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β‐synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trial
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Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β‐synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trial

Van Hove, Johan L. K ; Freehauf, Cynthia L ; Ficicioglu, Can ; Pena, Loren D. M ; Moreau, Kerrie L ; Henthorn, Thomas K ; Christians, Uwe ; Jiang, Hua ; Cowan, Tina M ; Young, Sarah P ; Hite, Michelle ; Friederich, Marisa W ; Stabler, Sally P ; Spector, Elaine B ; Kronquist, Kathryn E ; Thomas, Janet A ; Emmett, Peggy ; Harrington, Mary J ; Pyle, Laura ; Creadon‐Swindell, Geralyn ; Wempe, Michael F ; MacLean, Kenneth N

Journal of inherited metabolic disease, 2019-05, Vol.42 (3), p.424-437 [Peer Reviewed Journal]

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10
Oxidative Stress and the ER Stress Response in a Murine Model for Early-Stage Alcoholic Liver Disease
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Oxidative Stress and the ER Stress Response in a Murine Model for Early-Stage Alcoholic Liver Disease

Galligan, James J ; Smathers, Rebecca L ; Shearn, Colin T ; Fritz, Kristofer S ; Backos, Donald S ; Jiang, Hua ; Franklin, Christopher C ; Orlicky, David J ; MacLean, Kenneth N ; Petersen, Dennis R Stegeman, J. J

Journal of toxicology, 2012, Vol.2012, p.1-12 [Peer Reviewed Journal]

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