| Year |
Citation |
Score |
| 2021 |
Lin M, Roth RA, Kozel BA, Mecham RP, Halabi CM. Loss of Angiotensin II Type 2 Receptor Improves Blood Pressure in Elastin Insufficiency. Frontiers in Cardiovascular Medicine. 8: 782138. PMID 34790711 DOI: 10.3389/fcvm.2021.782138 |
0.447 |
|
| 2021 |
Troia A, Knutsen RH, Halabi CM, Malide D, Yu ZX, Wardlaw-Pickett A, Kronquist EK, Tsang KM, Kovacs A, Mecham RP, Kozel BA. Inhibition of NOX1 Mitigates Blood Pressure Increases in Elastin Insufficiency. Function (Oxford, England). 2: zqab015. PMID 34223172 DOI: 10.1093/function/zqab015 |
0.483 |
|
| 2020 |
Parrish PCR, Liu D, Knutsen RH, Billington CJ, Mecham RP, Fu YP, Kozel BA. Whole exome sequencing in patients with Williams-Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk. Human Molecular Genetics. PMID 32412588 DOI: 10.1093/Hmg/Ddaa093 |
0.536 |
|
| 2020 |
Dmitrieva NI, Walts AD, Nguyen DP, Grubb A, Zhang X, Wang X, Ping X, Jin H, Yu Z, Yu ZX, Yang D, Schwartzbeck R, Dalgard CL, Kozel BA, Levin MD, et al. Impaired angiogenesis and extracellular matrix metabolism in Autosomal-Dominant Hyper-IgE Syndrome. The Journal of Clinical Investigation. PMID 32369445 DOI: 10.1172/Jci135490 |
0.349 |
|
| 2020 |
Halabi CM, Kozel BA. Vascular elastic fiber heterogeneity in health and disease. Current Opinion in Hematology. PMID 32141894 DOI: 10.1097/Moh.0000000000000578 |
0.347 |
|
| 2020 |
Lugo M, Wong ZC, Billington CJ, Parrish PCR, Muldoon G, Liu D, Pober BR, Kozel BA. Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome. American Journal of Medical Genetics. Part A. PMID 32077592 DOI: 10.1002/Ajmg.A.61522 |
0.315 |
|
| 2019 |
Kozel BA, Mecham RP. Elastic Fiber Ultrastructure and Assembly. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 31669522 DOI: 10.1016/J.Matbio.2019.10.002 |
0.505 |
|
| 2018 |
Thompson E, Abdalla E, Superti-Furga A, McAlister W, Kratz L, Unger S, Royer-Bertrand B, Campos-Xavier B, Mittaz-Crettol L, Amin AK, DeSanto C, Wilson DB, Douglas G, Kozel B, Shinawi M. Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes. Bone. PMID 30448303 DOI: 10.1016/J.Bone.2018.11.006 |
0.327 |
|
| 2018 |
Lasio MLD, Kozel BA. Elastin-driven genetic diseases. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 29501665 DOI: 10.1016/J.Matbio.2018.02.021 |
0.386 |
|
| 2018 |
Knutsen R, Beeman SC, Broekelmann TJ, Liu D, Tsang KM, Kovacs A, Ye L, Danback J, Watson A, Wardlaw A, Wagenseil J, Garbow JR, Shoykhet M, Kozel BA. Minoxidil improves vascular compliance, restores cerebral blood flow and alters extracellular matrix gene expression in a model of chronic vascular stiffness. American Journal of Physiology. Heart and Circulatory Physiology. PMID 29498532 DOI: 10.1152/Ajpheart.00683.2017 |
0.331 |
|
| 2015 |
Halabi CM, Broekelmann TJ, Knutsen RH, Ye L, Mecham RP, Kozel BA. Chronic antihypertensive treatment improves pulse pressure but not large artery mechanics in a mouse model of congenital vascular stiffness. American Journal of Physiology. Heart and Circulatory Physiology. 309: H1008-16. PMID 26232234 DOI: 10.1152/Ajpheart.00288.2015 |
0.504 |
|
| 2014 |
DeMarsilis AJ, Walji TA, Maedeker JA, Stoka KV, Kozel BA, Mecham RP, Wagenseil JE, Craft CS. Elastin Insufficiency Predisposes Mice to Impaired Glucose Metabolism. Journal of Molecular and Genetic Medicine : An International Journal of Biomedical Research. 8. PMID 26167199 DOI: 10.4172/1747-0862.1000129 |
0.519 |
|
| 2014 |
Kozel BA, Bayliss SJ, Berk DR, Waxler JL, Knutsen RH, Danback JR, Pober BR. Skin findings in Williams syndrome. American Journal of Medical Genetics. Part A. 164: 2217-25. PMID 24920525 DOI: 10.1002/Ajmg.A.36628 |
0.326 |
|
| 2014 |
Cheng YW, Tan CA, Minor A, Arndt K, Wysinger L, Grange DK, Kozel BA, Robin NH, Waggoner D, Fitzpatrick C, Das S, Del Gaudio D. Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion. Molecular Genetics & Genomic Medicine. 2: 115-23. PMID 24689074 DOI: 10.1002/Mgg3.48 |
0.326 |
|
| 2014 |
Osei-Owusu P, Knutsen RH, Kozel BA, Dietrich HH, Blumer KJ, Mecham RP. Altered reactivity of resistance vasculature contributes to hypertension in elastin insufficiency. American Journal of Physiology. Heart and Circulatory Physiology. 306: H654-66. PMID 24414067 DOI: 10.1152/Ajpheart.00601.2013 |
0.498 |
|
| 2014 |
Kozel BA, Danback JR, Waxler JL, Knutsen RH, de Las Fuentes L, Reusz GS, Kis E, Bhatt AB, Pober BR. Williams syndrome predisposes to vascular stiffness modified by antihypertensive use and copy number changes in NCF1. Hypertension. 63: 74-9. PMID 24126171 DOI: 10.1161/Hypertensionaha.113.02087 |
0.356 |
|
| 2013 |
Schilter KF, Reis LM, Schneider A, Bardakjian TM, Abdul-Rahman O, Kozel BA, Zimmerman HH, Broeckel U, Semina EV. Whole-genome copy number variation analysis in anophthalmia and microphthalmia. Clinical Genetics. 84: 473-81. PMID 23701296 DOI: 10.1111/Cge.12202 |
0.32 |
|
| 2012 |
Sugitani H, Hirano E, Knutsen RH, Shifren A, Wagenseil JE, Ciliberto C, Kozel BA, Urban Z, Davis EC, Broekelmann TJ, Mecham RP. Alternative splicing and tissue-specific elastin misassembly act as biological modifiers of human elastin gene frameshift mutations associated with dominant cutis laxa. The Journal of Biological Chemistry. 287: 22055-67. PMID 22573328 DOI: 10.1074/Jbc.M111.327940 |
0.552 |
|
| 2011 |
Kozel BA, Knutsen RH, Ye L, Ciliberto CH, Broekelmann TJ, Mecham RP. Genetic modifiers of cardiovascular phenotype caused by elastin haploinsufficiency act by extrinsic noncomplementation. The Journal of Biological Chemistry. 286: 44926-36. PMID 22049077 DOI: 10.1074/Jbc.M111.274779 |
0.548 |
|
| 2011 |
Reis LM, Tyler RC, Schilter KF, Abdul-Rahman O, Innis JW, Kozel BA, Schneider AS, Bardakjian TM, Lose EJ, Martin DM, Broeckel U, Semina EV. BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome. Human Genetics. 130: 495-504. PMID 21340693 DOI: 10.1007/S00439-011-0968-Y |
0.302 |
|
| 2010 |
Shinawi M, Liu P, Kang SH, Shen J, Belmont JW, Scott DA, Probst FJ, Craigen WJ, Graham BH, Pursley A, Clark G, Lee J, Proud M, Stocco A, Rodriguez DL, ... Kozel BA, et al. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. Journal of Medical Genetics. 47: 332-41. PMID 19914906 DOI: 10.1136/Jmg.2009.073015 |
0.3 |
|
| 2006 |
Czirok A, Zach J, Kozel BA, Mecham RP, Davis EC, Rongish BJ. Elastic fiber macro-assembly is a hierarchical, cell motion-mediated process. Journal of Cellular Physiology. 207: 97-106. PMID 16331676 DOI: 10.1002/Jcp.20573 |
0.516 |
|
| 2006 |
Kozel BA, Rongish BJ, Czirok A, Zach J, Little CD, Davis EC, Knutsen RH, Wagenseil JE, Levy MA, Mecham RP. Elastic fiber formation: a dynamic view of extracellular matrix assembly using timer reporters. Journal of Cellular Physiology. 207: 87-96. PMID 16261592 DOI: 10.1002/Jcp.20546 |
0.518 |
|
| 2005 |
Broekelmann TJ, Kozel BA, Ishibashi H, Werneck CC, Keeley FW, Zhang L, Mecham RP. Tropoelastin interacts with cell-surface glycosaminoglycans via its COOH-terminal domain. The Journal of Biological Chemistry. 280: 40939-47. PMID 16192266 DOI: 10.1074/Jbc.M507309200 |
0.467 |
|
| 2004 |
Kozel BA, Ciliberto CH, Mecham RP. Deposition of tropoelastin into the extracellular matrix requires a competent elastic fiber scaffold but not live cells. Matrix Biology : Journal of the International Society For Matrix Biology. 23: 23-34. PMID 15172035 DOI: 10.1016/J.Matbio.2004.02.004 |
0.515 |
|
| 2003 |
Kozel BA, Wachi H, Davis EC, Mecham RP. Domains in tropoelastin that mediate elastin deposition in vitro and in vivo. The Journal of Biological Chemistry. 278: 18491-8. PMID 12626514 DOI: 10.1074/Jbc.M212715200 |
0.515 |
|
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