| Year |
Citation |
Score |
| 2020 |
Thoene JG, DelMonte MA, Mullet J. Microvesicle delivery of a lysosomal transport protein to ex vivo rabbit cornea. Molecular Genetics and Metabolism Reports. 23: 100587. PMID 32280591 DOI: 10.1016/j.ymgmr.2020.100587 |
0.307 |
|
| 2013 |
Thoene J, Goss T, Witcher M, Mullet J, N'Kuli F, Van Der Smissen P, Courtoy P, Hahn SH. In vitro correction of disorders of lysosomal transport by microvesicles derived from baculovirus-infected Spodoptera cells. Molecular Genetics and Metabolism. 109: 77-85. PMID 23465695 DOI: 10.1016/J.Ymgme.2013.01.014 |
0.401 |
|
| 2011 |
Thoene J, Witcher M, Mullet J. Sf9 cell vesicle-mediated correction of cystine storage in cystinotic fibroblasts and sialic acid storage in infantile sialic acid storage disease fibroblasts Molecular Genetics and Metabolism. 102: S42-S43. DOI: 10.1016/J.Ymgme.2010.11.143 |
0.324 |
|
| 2010 |
Vitvitsky V, Witcher M, Banerjee R, Thoene J. The redox status of cystinotic fibroblasts. Molecular Genetics and Metabolism. 99: 384-8. PMID 20061170 DOI: 10.1016/J.Ymgme.2009.12.010 |
0.378 |
|
| 2006 |
Park MA, Pejovic V, Kerisit KG, Junius S, Thoene JG. Increased apoptosis in cystinotic fibroblasts and renal proximal tubule epithelial cells results from cysteinylation of protein kinase Cdelta. Journal of the American Society of Nephrology : Jasn. 17: 3167-75. PMID 17021265 DOI: 10.1681/ASN.2006050474 |
0.336 |
|
| 2005 |
Park MA, Thoene JG. Potential role of apoptosis in development of the cystinotic phenotype. Pediatric Nephrology (Berlin, Germany). 20: 441-6. PMID 15622500 DOI: 10.1007/s00467-004-1712-9 |
0.356 |
|
| 2004 |
Helip-Wooley A, Thoene JG. Sucrose-induced vacuolation results in increased expression of cholesterol biosynthesis and lysosomal genes. Experimental Cell Research. 292: 89-100. PMID 14720509 DOI: 10.1016/J.Yexcr.2003.09.003 |
0.612 |
|
| 2002 |
Park M, Helip-Wooley A, Thoene J. Lysosomal cystine storage augments apoptosis in cultured human fibroblasts and renal tubular epithelial cells. Journal of the American Society of Nephrology : Jasn. 13: 2878-87. PMID 12444206 DOI: 10.1097/01.Asn.0000036867.49866.59 |
0.601 |
|
| 2002 |
Helip-Wooley A, Park MA, Lemons RM, Thoene JG. Expression of CTNS alleles: subcellular localization and aminoglycoside correction in vitro. Molecular Genetics and Metabolism. 75: 128-33. PMID 11855931 DOI: 10.1006/mgme.2001.3272 |
0.608 |
|
| 2001 |
Kleta R, Anikster Y, Lucero C, Shotelersuk V, Huizing M, Bernardini I, Park M, Thoene J, Schneider J, Gahl WA. CTNS mutations in African American patients with cystinosis. Molecular Genetics and Metabolism. 74: 332-7. PMID 11708862 DOI: 10.1006/Mgme.2001.3218 |
0.361 |
|
| 2000 |
Anikster Y, Lucero C, Guo J, Huizing M, Shotelersuk V, Bernardini I, McDowell G, Iwata F, Kaiser-Kupfer MI, Jaffe R, Thoene J, Schneider JA, Gahl WA. Ocular nonnephropathic cystinosis: clinical, biochemical, and molecular correlations. Pediatric Research. 47: 17-23. PMID 10625078 DOI: 10.1203/00006450-200001000-00007 |
0.403 |
|
| 2000 |
Thoene J, Lemons R. Correction of the Cystinotic Phenotype in Cultured Cells by an Aminoglycoside Genetics in Medicine. 2: 74-74. DOI: 10.1097/00125817-200001000-00082 |
0.466 |
|
| 1999 |
Thoene J, Lemons R, Anikster Y, Mullet J, Paelicke K, Lucero C, Gahl W, Schneider J, Shu SG, Campbell HT. Mutations of CTNS causing intermediate cystinosis. Molecular Genetics and Metabolism. 67: 283-93. PMID 10444339 DOI: 10.1006/Mgme.1999.2876 |
0.365 |
|
| 1998 |
Shotelersuk V, Larson D, Anikster Y, McDowell G, Lemons R, Bernardini I, Guo J, Thoene J, Gahl WA. CTNS mutations in an American-based population of cystinosis patients. American Journal of Human Genetics. 63: 1352-62. PMID 9792862 DOI: 10.1086/302118 |
0.394 |
|
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