Michael J. Kern - Publications

Affiliations: 
Medical University of South Carolina, Charleston, SC, United States 
Area:
Molecular Biology, Biochemistry

30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Ding L, Shunkwiler LB, Harper NW, Zhao Y, Hinohara K, Huh SJ, Ekram MB, Guz J, Kern MJ, Awgulewitsch A, Shull JD, Smits BMG, Polyak K. Deletion of Cdkn1b in ACI rats leads to increased proliferation and pregnancy-associated changes in the mammary gland due to perturbed systemic endocrine environment. Plos Genetics. 15: e1008002. PMID 30893315 DOI: 10.1371/Journal.Pgen.1008002  0.323
2015 Potter CS, Kern MJ, Baybo MA, Pruett ND, Godwin AR, Sundberg JP, Awgulewitsch A. Dysregulated expression of sterol O-acyltransferase 1 (Soat1) in the hair shaft of Hoxc13 null mice. Experimental and Molecular Pathology. 99: 441-4. PMID 26321246 DOI: 10.1016/J.Yexmp.2015.08.016  0.491
2014 Claussnitzer M, Dankel SN, Klocke B, Grallert H, Glunk V, Berulava T, Lee H, Oskolkov N, Fadista J, Ehlers K, Wahl S, Hoffmann C, Qian K, Rönn T, Riess H, ... ... Kern MJ, et al. Leveraging cross-species transcription factor binding site patterns: from diabetes risk loci to disease mechanisms. Cell. 156: 343-58. PMID 24439387 DOI: 10.1016/J.Cell.2013.10.058  0.311
2012 Sugi Y, Kern MJ, Markwald RR, Burnside JL. Periostin Expression is Altered in Aortic Valves in Smad6 Mutant Mice. Journal of Neonatal Biology. 1. PMID 25383261 DOI: 10.4172/2167-0897.1000101  0.615
2012 Pruett ND, Hajdu Z, Zhang J, Visconti RP, Kern MJ, Wellik DM, Majesky MW, Awgulewitsch A. Changing topographic Hox expression in blood vessels results in regionally distinct vessel wall remodeling. Biology Open. 1: 430-5. PMID 23213434 DOI: 10.1242/Bio.2012039  0.416
2012 Griffin AC, Kern MJ, Kirkwood KL. MKP-1 is essential for canonical vitamin D-induced signaling through nuclear import and regulates RANKL expression and function. Molecular Endocrinology (Baltimore, Md.). 26: 1682-93. PMID 22899855 DOI: 10.1210/Me.2012-1033  0.303
2012 Kern MJ, Argao EA, Potter SS. Homeobox genes and heart development. Trends in Cardiovascular Medicine. 5: 47-54. PMID 21232237 DOI: 10.1016/1050-1738(94)00033-6  0.343
2011 Potter KA, Kern MJ, Fullbright G, Bielawski J, Scherer SS, Yum SW, Li JJ, Cheng H, Han X, Venkata JK, Khan PA, Rohrer B, Hama H. Central nervous system dysfunction in a mouse model of FA2H deficiency. Glia. 59: 1009-21. PMID 21491498 DOI: 10.1002/Glia.21172  0.32
2011 Potter CS, Pruett ND, Kern MJ, Baybo MA, Godwin AR, Potter KA, Peterson RL, Sundberg JP, Awgulewitsch A. The nude mutant gene Foxn1 is a HOXC13 regulatory target during hair follicle and nail differentiation. The Journal of Investigative Dermatology. 131: 828-37. PMID 21191399 DOI: 10.1038/Jid.2010.391  0.466
2011 Lu X, Beck GR, Gilbert LC, Camalier CE, Bateman NW, Hood BL, Conrads TP, Kern MJ, You S, Chen H, Nanes MS. Identification of the homeobox protein Prx1 (MHox, Prrx-1) as a regulator of osterix expression and mediator of tumor necrosis factor α action in osteoblast differentiation. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 26: 209-19. PMID 20683885 DOI: 10.1002/Jbmr.203  0.423
2011 Gruber HE, Norris RA, Kern MJ, Hoelscher GL, Ingram JA, Zinchenko N, Hanley EN. Periostin is expressed by cells of the human and sand rat intervertebral discs. Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission. 86: 199-206. PMID 20370359 DOI: 10.3109/10520291003722774  0.606
2010 Haviland S, Cleemann L, McQuinn T, Kern M, Morad M. Expression and Regulation of Shark NCX Gene in Transgenic Mouse Heart Biophysical Journal. 98: 677a. DOI: 10.1016/J.Bpj.2009.12.3721  0.498
2009 Norris RA, Potts JD, Yost MJ, Junor L, Brooks T, Tan H, Hoffman S, Hart MM, Kern MJ, Damon B, Markwald RR, Goodwin RL. Periostin promotes a fibroblastic lineage pathway in atrioventricular valve progenitor cells Developmental Dynamics. 238: 1052-1063. PMID 19334280 DOI: 10.1002/Dvdy.21933  0.717
2009 Potter CS, Potter KA, Pruett ND, Kern MJ, Godwin AA, Sundberg JP, Awgulewitsch A. Hoxc13 regulation of Soat1 in the hippocampus and cerebellum Developmental Biology. 331: 439-440. DOI: 10.1016/J.Ydbio.2009.05.194  0.304
2007 Higuchi T, Bartel FO, Masuya M, Deguchi T, Henderson KW, Li R, Muise-Helmericks RC, Kern MJ, Watson DK, Spyropoulos DD. Thymomegaly, microsplenia, and defective homeostatic proliferation of peripheral lymphocytes in p51-Ets1 isoform-specific null mice. Molecular and Cellular Biology. 27: 3353-66. PMID 17339335 DOI: 10.1128/Mcb.01871-06  0.364
2007 Jin L, Kern MJ, Otey CA, Wamhoff BR, Somlyo AV. Angiotensin II, focal adhesion kinase, and PRX1 enhance smooth muscle expression of lipoma preferred partner and its newly identified binding partner palladin to promote cell migration. Circulation Research. 100: 817-25. PMID 17322171 DOI: 10.1161/01.Res.0000261351.54147.De  0.411
2006 Chapados R, Abe K, Ihida-Stansbury K, McKean D, Gates AT, Kern M, Merklinger S, Elliott J, Plant A, Shimokawa H, Jones PL. ROCK controls matrix synthesis in vascular smooth muscle cells: Coupling vasoconstriction to vascular remodeling Circulation Research. 99: 837-844. PMID 16990566 DOI: 10.1161/01.Res.0000246172.77441.F1  0.326
2006 Potter CS, Peterson RL, Barth JL, Pruett ND, Jacobs DF, Kern MJ, Argraves WS, Sundberg JP, Awgulewitsch A. Evidence that the satin hair mutant gene Foxq1 is among multiple and functionally diverse regulatory targets for Hoxc13 during hair follicle differentiation. The Journal of Biological Chemistry. 281: 29245-55. PMID 16835220 DOI: 10.1074/Jbc.M603646200  0.483
2005 Peterson RE, Hoffman S, Kern MJ. Opposing roles of two isoforms of the Prx1 homeobox gene in chondrogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 233: 811-21. PMID 15895367 DOI: 10.1002/Dvdy.20412  0.444
2003 McKean DM, Sisbarro L, Ilic D, Kaplan-Alburquerque N, Nemenoff R, Weiser-Evans M, Kern MJ, Jones PL. FAK induces expression of Prx1 to promote tenascin-C-dependent fibroblast migration. The Journal of Cell Biology. 161: 393-402. PMID 12741393 DOI: 10.1083/Jcb.Jcb.200302126  0.37
2003 Scott KK, Norris RA, Potter SS, Norrington DW, Baybo MA, Hicklin DM, Kern MJ. GeneChip microarrays facilitate identification of Protease Nexin-1 as a target gene of the Prx2 (S8) homeoprotein. Dna and Cell Biology. 22: 95-105. PMID 12713735 DOI: 10.1089/104454903321515904  0.648
2002 Chesterman ES, Kern MJ. Comparative analysis of Prx1 and Prx2 expression in mice provides evidence for incomplete compensation. The Anatomical Record. 266: 1-4. PMID 11748565 DOI: 10.1002/Ar.10028  0.685
2001 Mjaatvedt CH, Nakaoka T, Moreno-Rodriguez R, Norris RA, Kern MJ, Eisenberg CA, Turner D, Markwald RR. The outflow tract of the heart is recruited from a novel heart-forming field. Developmental Biology. 238: 97-109. PMID 11783996 DOI: 10.1006/Dbio.2001.0409  0.639
2001 Chesterman ES, Gainey GD, Varn AC, Peterson RE, Kern MJ. Investigation of Prx1 protein expression provides evidence for conservation of cardiac-specific posttranscriptional regulation in vertebrates. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 222: 459-70. PMID 11747080 DOI: 10.1002/Dvdy.1198  0.691
2001 Norris RA, Kern MJ. The identification of Prx1 transcription regulatory domains provides a mechanism for unequal compensation by the Prx1 and Prx2 loci. The Journal of Biological Chemistry. 276: 26829-37. PMID 11373278 DOI: 10.1074/Jbc.M100239200  0.579
2001 Norris RA, Kern MJ. Identification of domains mediating transcription activation, repression, and inhibition in the paired-related homeobox protein, Prx2 (S8). Dna and Cell Biology. 20: 89-99. PMID 11244566 DOI: 10.1089/104454901750070292  0.62
2000 Norris RA, Scott KK, Moore CS, Stetten G, Brown CR, Jabs EW, Wulfsberg EA, Yu J, Kern MJ. Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 1000-5. PMID 11063257 DOI: 10.1007/S003350010193  0.633
2000 Bergwerff M, Gittenberger-de Groot AC, Wisse LJ, DeRuiter MC, Wessels A, Martin JF, Olson EN, Kern MJ. Loss of function of the Prx1 and Prx2 homeobox genes alters architecture of the great elastic arteries and ductus arteriosus. Virchows Archiv : An International Journal of Pathology. 436: 12-9. PMID 10664157 DOI: 10.1007/Pl00008193  0.453
1999 Lu MF, Cheng HT, Lacy AR, Kern MJ, Argao EA, Potter SS, Olson EN, Martin JF. Paired-related homeobox genes cooperate in handplate and hindlimb zeugopod morphogenesis. Developmental Biology. 205: 145-57. PMID 9882503 DOI: 10.1006/Dbio.1998.9116  0.474
1994 Kern MJ, Argao EA, Birkenmeier EH, Rowe LB, Potter SS. Genomic organization and chromosome localization of the murine homeobox gene Pmx. Genomics. 19: 334-40. PMID 7910581 DOI: 10.1006/geno.1994.1066  0.33
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