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Charlotte L. Phillips - Publications

Affiliations: 
University of Missouri - Columbia, Columbia, MO, United States 
Area:
Biochemistry
Website:
https://biochem.missouri.edu/faculty/faculty-members/phillipsc/index.php

42 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
2020 Oestreich AK, DeCata JA, Akers JD, Phillips CL, Schulz LC. Fecundity is impaired in a mouse model of osteogenesis imperfecta. Molecular Reproduction and Development. PMID 32869432 DOI: 10.1002/mrd.23416  0.48
2020 Oestreich AK, Onuzuriuke A, Yao X, Talton O, Wang Y, Pfeiffer FM, Schulz LC, Phillips CL. Leprdb/+ dams protect wildtype male offspring bone strength from the detrimental effects of high fat diet. Endocrinology. PMID 32484851 DOI: 10.1210/endocr/bqaa087  0.48
2018 Jeong Y, Daghlas SA, Yixia X, Hulbert MA, Pfeiffer FM, Dallas MR, Omosule CL, Pearsall RS, Dallas SL, Phillips CL. Skeletal Response to Soluble Activin Receptor Type IIB in Mouse Models of Osteogenesis Imperfecta. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 29813187 DOI: 10.1002/jbmr.3473  0.48
2017 Brodeur AC, Roberts-Pilgrim AM, Thompson KL, Franklin CL, Phillips CL. Transforming growth factor-β1/Smad3-independent epithelial-mesenchymal transition in type I collagen glomerulopathy. International Journal of Nephrology and Renovascular Disease. 10: 251-259. PMID 28919801 DOI: 10.2147/IJNRD.S141393  0.64
2017 Jeong Y, Daghlas SA, Kahveci AS, Salamango D, Gentry BA, Brown M, Rector RS, Pearsall RS, Phillips CL. Soluble activin receptor type IIB decoy receptor differentially impacts murine osteogenesis imperfecta muscle function. Muscle & Nerve. PMID 28555931 DOI: 10.1002/mus.25706  0.6
2016 Oestreich AK, Kamp WM, McCray MG, Carleton SM, Karasseva N, Lenz KL, Jeong Y, Daghlas SA, Yao X, Wang Y, Pfeiffer FM, Ellersieck MR, Schulz LC, Phillips CL. Decreasing maternal myostatin programs adult offspring bone strength in a mouse model of osteogenesis imperfecta. Proceedings of the National Academy of Sciences of the United States of America. PMID 27821779 DOI: 10.1073/pnas.1607644113  0.76
2016 Mirigian LS, Makareeva E, Mertz EL, Omari S, Roberts-Pilgrim AM, Oestreich AK, Phillips CL, Leikin S. Osteoblast Malfunction Caused by Cell Stress Response to Procollagen Misfolding in α2(I)-G610C Mouse Model of Osteogenesis Imperfecta. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 26925839 DOI: 10.1002/jbmr.2824  0.76
2015 Oestreich AK, Garcia MR, Yao X, Pfeiffer FM, Nobakhti S, Shefelbine SJ, Wang Y, Brodeur AC, Phillips CL. Characterization of the MPS I-H knock-in mouse reveals increased femoral biomechanical integrity with compromised material strength and altered bone geometry. Molecular Genetics and Metabolism Reports. 5: 3-11. PMID 28649535 DOI: 10.1016/j.ymgmr.2015.08.004  0.64
2015 Oestreich AK, Carleton SM, Yao X, Gentry BA, Raw CE, Brown M, Pfeiffer FM, Wang Y, Phillips CL. Myostatin deficiency partially rescues the bone phenotype of osteogenesis imperfecta model mice. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. PMID 26179666 DOI: 10.1007/s00198-015-3226-7  0.76
2015 Park AC, Phillips CL, Pfeiffer FM, Roenneburg DA, Kernien JF, Adams SM, Davidson JM, Birk DE, Greenspan DS. Homozygosity and Heterozygosity for Null Col5a2 Alleles Produce Embryonic Lethality and a Novel Classic Ehlers-Danlos Syndrome-Related Phenotype. The American Journal of Pathology. 185: 2000-11. PMID 25987251 DOI: 10.1016/j.ajpath.2015.03.022  0.76
2015 Jeong Y, Carleton SM, Gentry BA, Yao X, Ferreira JA, Salamango DJ, Weis M, Oestreich AK, Williams AM, McCray MG, Eyre DR, Brown M, Wang Y, Phillips CL. Hindlimb Skeletal Muscle Function and Skeletal Quality and Strength in +/G610C Mice With and Without Weight-Bearing Exercise. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 25829218 DOI: 10.1002/jbmr.2518  0.76
2013 Yao X, Carleton SM, Kettle AD, Melander J, Phillips CL, Wang Y. Gender-dependence of bone structure and properties in adult osteogenesis imperfecta murine model. Annals of Biomedical Engineering. 41: 1139-49. PMID 23536112 DOI: 10.1007/s10439-013-0793-7  0.76
2013 Phillips CL, Carleton SM, Gentry BA. Animal Models of Osteogenesis Imperfecta Osteogenesis Imperfecta: a Translational Approach to Brittle Bone Disease. 197-207. DOI: 10.1016/B978-0-12-397165-4.00021-6  0.76
2012 Otsuru S, Gordon PL, Shimono K, Jethva R, Marino R, Phillips CL, Hofmann TJ, Veronesi E, Dominici M, Iwamoto M, Horwitz EM. Transplanted bone marrow mononuclear cells and MSCs impart clinical benefit to children with osteogenesis imperfecta through different mechanisms. Blood. 120: 1933-41. PMID 22829629 DOI: 10.1182/blood-2011-12-400085  0.76
2012 Pennington KA, Harper JL, Sigafoos AN, Beffa LM, Carleton SM, Phillips CL, Schulz LC. Effect of food restriction and leptin supplementation on fetal programming in mice. Endocrinology. 153: 4556-67. PMID 22778222 DOI: 10.1210/en.2012-1119  0.76
2012 Pelch KE, Carleton SM, Phillips CL, Nagel SC. Developmental exposure to xenoestrogens at low doses alters femur length and tensile strength in adult mice. Biology of Reproduction. 86: 69. PMID 22088916 DOI: 10.1095/biolreprod.111.096545  0.76
2011 Roberts-Pilgrim AM, Makareeva E, Myles MH, Besch-Williford CL, Brodeur AC, Walker AL, Leikin S, Franklin CL, Phillips CL. Deficient degradation of homotrimeric type I collagen, α1(I)3 glomerulopathy in oim mice. Molecular Genetics and Metabolism. 104: 373-82. PMID 21855382 DOI: 10.1016/j.ymgme.2011.07.025  0.76
2011 Gentry BA, Ferreira JA, Phillips CL, Brown M. Hindlimb skeletal muscle function in myostatin-deficient mice. Muscle & Nerve. 43: 49-57. PMID 21082689 DOI: 10.1002/mus.21796  0.76
2010 Carleton SM, Whitford GM, Phillips CL. Dietary fluoride restriction does not alter femoral biomechanical strength in col1a2-deficient (oim) mice with type I collagen glomerulopathy. The Journal of Nutrition. 140: 1752-6. PMID 20724489 DOI: 10.3945/jn.109.120261  0.76
2010 Gentry BA, Ferreira JA, McCambridge AJ, Brown M, Phillips CL. Skeletal muscle weakness in osteogenesis imperfecta mice. Matrix Biology : Journal of the International Society For Matrix Biology. 29: 638-44. PMID 20619344 DOI: 10.1016/j.matbio.2010.06.006  0.76
2010 Han S, Makareeva E, Kuznetsova NV, DeRidder AM, Sutter MB, Losert W, Phillips CL, Visse R, Nagase H, Leikin S. Molecular mechanism of type I collagen homotrimer resistance to mammalian collagenases. The Journal of Biological Chemistry. 285: 22276-81. PMID 20463013 DOI: 10.1074/jbc.M110.102079  0.76
2010 Makareeva E, Han S, Vera JC, Sackett DL, Holmbeck K, Phillips CL, Visse R, Nagase H, Leikin S. Carcinomas contain a matrix metalloproteinase-resistant isoform of type I collagen exerting selective support to invasion. Cancer Research. 70: 4366-74. PMID 20460529 DOI: 10.1158/0008-5472.CAN-09-4057  0.76
2010 Carleton SM, Peck DS, Grasela J, Dietiker KL, Phillips CL. DNA carrier testing and newborn screening for maple syrup urine disease in Old Order Mennonite communities. Genetic Testing and Molecular Biomarkers. 14: 205-8. PMID 20136525 DOI: 10.1089/gtmb.2009.0107  0.76
2010 Daley E, Streeten EA, Sorkin JD, Kuznetsova N, Shapses SA, Carleton SM, Shuldiner AR, Marini JC, Phillips CL, Goldstein SA, Leikin S, McBride DJ. Variable bone fragility associated with an Amish COL1A2 variant and a knock-in mouse model. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 247-61. PMID 19594296 DOI: 10.1359/jbmr.090720  0.76
2008 Carleton SM, McBride DJ, Carson WL, Huntington CE, Twenter KL, Rolwes KM, Winkelmann CT, Morris JS, Taylor JF, Phillips CL. Role of genetic background in determining phenotypic severity throughout postnatal development and at peak bone mass in Col1a2 deficient mice (oim). Bone. 42: 681-94. PMID 18313376 DOI: 10.1016/j.bone.2007.12.215  0.76
2007 Nordstrom SM, Carleton SM, Carson WL, Eren M, Phillips CL, Vaughan DE. Transgenic over-expression of plasminogen activator inhibitor-1 results in age-dependent and gender-specific increases in bone strength and mineralization. Bone. 41: 995-1004. PMID 17888748 DOI: 10.1016/j.bone.2007.08.020  0.76
2007 Brodeur AC, Wirth DA, Franklin CL, Reneker LW, Miner JH, Phillips CL. Type I collagen glomerulopathy: postnatal collagen deposition follows glomerular maturation. Kidney International. 71: 985-93. PMID 17361118 DOI: 10.1038/sj.ki.5002173  0.76
2006 Wenstrup RJ, Florer JB, Davidson JM, Phillips CL, Pfeiffer BJ, Menezes DW, Chervoneva I, Birk DE. Murine model of the Ehlers-Danlos syndrome. col5a1 haploinsufficiency disrupts collagen fibril assembly at multiple stages. The Journal of Biological Chemistry. 281: 12888-95. PMID 16492673 DOI: 10.1074/jbc.M511528200  0.76
2005 Pfeiffer BJ, Franklin CL, Hsieh FH, Bank RA, Phillips CL. Alpha 2(I) collagen deficient oim mice have altered biomechanical integrity, collagen content, and collagen crosslinking of their thoracic aorta. Matrix Biology : Journal of the International Society For Matrix Biology. 24: 451-8. PMID 16095890 DOI: 10.1016/j.matbio.2005.07.001  0.76
2004 Graham JS, Vomund AN, Phillips CL, Grandbois M. Structural changes in human type I collagen fibrils investigated by force spectroscopy. Experimental Cell Research. 299: 335-42. PMID 15350533 DOI: 10.1016/j.yexcr.2004.05.022  0.76
2004 Vomund AN, Braddock SR, Krause GF, Phillips CL. Potential modifier role of the R618Q variant of proalpha2(I)collagen in type I collagen fibrillogenesis: in vitro assembly analysis. Molecular Genetics and Metabolism. 82: 144-53. PMID 15172002 DOI: 10.1016/j.ymgme.2004.03.004  0.76
2002 Phillips CL, Pfeiffer BJ, Luger AM, Franklin CL. Novel collagen glomerulopathy in a homotrimeric type I collagen mouse (oim). Kidney International. 62: 383-91. PMID 12109999 DOI: 10.1046/j.1523-1755.2002.00451.x  0.76
2002 Love-Gregory LD, Grasela J, Hillman RE, Phillips CL. Evidence of common ancestry for the maple syrup urine disease (MSUD) Y438N allele in non-Mennonite MSUD patients. Molecular Genetics and Metabolism. 75: 79-90. PMID 11825067 DOI: 10.1006/mgme.2001.3264  0.76
2001 Love-Gregory LD, Dyer JA, Grasela J, Hillman RE, Phillips CL. Carrier detection and rapid newborn diagnostic test for the common Y393N maple syrup urine disease allele by PCR-RFLP: culturally permissible testing in the Mennonite community. Journal of Inherited Metabolic Disease. 24: 393-403. PMID 11486905 DOI: 10.1023/A:1010517005001  0.76
2001 Vouyouka AG, Pfeiffer BJ, Liem TK, Taylor TA, Mudaliar J, Phillips CL. The role of type I collagen in aortic wall strength with a homotrimeric. Journal of Vascular Surgery. 33: 1263-70. PMID 11389427 DOI: 10.1067/mva.2001.113579  0.76
1994 Phillips CL, Combs SB, Pinnell SR. Effects of ascorbic acid on proliferation and collagen synthesis in relation to the donor age of human dermal fibroblasts. The Journal of Investigative Dermatology. 103: 228-32. PMID 7518857 DOI: 10.1111/1523-1747.ep12393187  0.76
1992 Phillips CL, Tajima S, Pinnell SR. Ascorbic acid and transforming growth factor-β1 increase collagen biosynthesis via different mechanisms: Coordinate regulation of proα1(I) and proα1(III) collagens Archives of Biochemistry and Biophysics. 295: 397-403. PMID 1586167 DOI: 10.1016/0003-9861(92)90533-3  0.76
1992 Phillips CL, Morgan AL, Lever LW, Wenstrup RJ. Sequence analysis of a full-length cDNA for the murine pro alpha 2(I) collagen chain: comparison of the derived primary structure with human pro alpha 2(I) collagen. Genomics. 13: 1345-6. PMID 1505972 DOI: 10.1016/0888-7543(92)90065-Z  0.76
1991 Phillips CL, Lever LW, Pinnell SR, Quarles LD, Wenstrup RJ. Construction of a full-length murine Proα2(I) collagen cDNA by the polymerase chain reaction Journal of Investigative Dermatology. 97: 980-984. PMID 1748823 DOI: 10.1111/1523-1747.ep12491894  0.76
1990 Phillips CL, Shrago-Howe AW, Pinnell SR, Wenstrup RJ. A substitution at a non-glycine position in the triple-helical domain of proα2(I) collagen chains present in an individual with a variant of the Marfan syndrome Journal of Clinical Investigation. 86: 1723-1728. PMID 1978725 DOI: 10.1172/JCI114897  0.76
1990 Phillips CL, Shrago AW, Pinnell SR, Wenstrup RJ. DNA sequence analysis of alpha 2(I) collagen from an individual with the Marfan phenotype Annals of the New York Academy of Sciences. 580: 560-561. DOI: 10.1111/j.1749-6632.1990.tb17992.x  0.76
1988 Phillips CL, Lin LW, Wu JC, Guzman K, Milsted A, Miller WL. 17β-estradiol and progesterone inhibit transcription of the genes encoding the subunits of ovine follicle-stimulating hormone Molecular Endocrinology. 2: 641-649. PMID 2457801 DOI: 10.1210/mend-2-7-641  0.76
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