| Year |
Citation |
Score |
| 2024 |
Karan G, Sahu S, Metya A, Maji MS. Asymmetric 1,2-Migration on Vicinal Tetrasubstituted Stereocenters Constructed from α-Keto Imines. Angewandte Chemie (International Ed. in English). e202405212. PMID 38721919 DOI: 10.1002/anie.202405212 |
0.367 |
|
| 2022 |
Sahu S, Karan G, Roy L, Maji MS. An expeditious route to sterically encumbered nonproteinogenic α-amino acid precursors using allylboronic acids. Chemical Science. 13: 2355-2362. PMID 35310508 DOI: 10.1039/d1sc06259j |
0.594 |
|
| 2021 |
Karan G, Sahu S, Maji MS. A one-pot "back-to-front" approach for the synthesis of benzene ring substituted indoles using allylboronic acids. Chemical Communications (Cambridge, England). PMID 33908966 DOI: 10.1039/d1cc01512e |
0.594 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2005 |
Karan G, Yang Z, Howes K, Zhao Y, Chen Y, Cameron DJ, Lin Y, Pearson E, Zhang K. Loss of ER retention and sequestration of the wild-type ELOVL4 by Stargardt disease dominant negative mutants. Molecular Vision. 11: 657-64. PMID 16145543 |
0.14 |
|
| 2003 |
Zhang XM, Yang Z, Karan G, Hashimoto T, Baehr W, Yang XJ, Zhang K. Elovl4 mRNA distribution in the developing mouse retina and phylogenetic conservation of Elovl4 genes. Molecular Vision. 9: 301-7. PMID 12847421 |
0.136 |
|
| 2004 |
Karan G, Yang Z, Zhang K. Expression of wild type and mutant ELOVL4 in cell culture: subcellular localization and cell viability. Molecular Vision. 10: 248-53. PMID 15073583 |
0.125 |
|
| 2005 |
Yang Z, Alvarez BV, Chakarova C, Jiang L, Karan G, Frederick JM, Zhao Y, Sauvé Y, Li X, Zrenner E, Wissinger B, Hollander AI, Katz B, Baehr W, Cremers FP, et al. Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration. Human Molecular Genetics. 14: 255-65. PMID 15563508 DOI: 10.1093/Hmg/Ddi023 |
0.121 |
|
| 2007 |
Li W, Chen Y, Cameron DJ, Wang C, Karan G, Yang Z, Zhao Y, Pearson E, Chen H, Deng C, Howes K, Zhang K. Elovl4 haploinsufficiency does not induce early onset retinal degeneration in mice. Vision Research. 47: 714-22. PMID 17254625 DOI: 10.1016/j.visres.2006.10.023 |
0.12 |
|
| 2005 |
Karan G, Lillo C, Yang Z, Cameron DJ, Locke KG, Zhao Y, Thirumalaichary S, Li C, Birch DG, Vollmer-Snarr HR, Williams DS, Zhang K. Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 102: 4164-9. PMID 15749821 DOI: 10.1073/Pnas.0407698102 |
0.119 |
|
| 2006 |
Moshfeghi DM, Yang Z, Faulkner ND, Karan G, Thirumalaichary S, Pearson E, Zhao Y, Tsai T, Zhang K. Choroidal neovascularization in patients with adult-onset foveomacular dystrophy caused by mutations in the RDS/peripherin gene. Advances in Experimental Medicine and Biology. 572: 35-40. PMID 17249552 DOI: 10.1007/0-387-32442-9_6 |
0.112 |
|
| 2008 |
Chattopadhyay S, Karan G, Sen I, Sen GC. A small region in the angiotensin-converting enzyme distal ectodomain is required for cleavage-secretion of the protein at the plasma membrane. Biochemistry. 47: 8335-41. PMID 18636749 DOI: 10.1021/Bi800702A |
0.112 |
|
| 2005 |
Jana S, Karan G, Deb JK. Purification of streptomycin adenylyltransferase from a recombinant Escherichia coli. Protein Expression and Purification. 40: 86-90. PMID 15721775 DOI: 10.1016/j.pep.2004.10.005 |
0.108 |
|
| 2004 |
Yang Z, Li Y, Jiang L, Karan G, Moshfeghi DM, O'Connor ST, Li X, Yu Z, Lewis H, Zack DJ, Jacobson SG, Zhang K. A novel RDS/peripherin gene mutation associated with diverse macular phenotypes Ophthalmic Genetics. 25: 133-145. PMID 15370544 DOI: 10.1080/13816810490514388 |
0.108 |
|
| 2016 |
Hu S, Ueda M, Stetson L, Ignatz-Hoover J, Moreton S, Chakrabarti A, Xia Z, Karan G, de Lima M, Agarwal MK, Wald DN. A novel glycogen synthase kinase-3 inhibitor optimized for acute myeloid leukemia differentiation activity. Molecular Cancer Therapeutics. PMID 27196775 DOI: 10.1158/1535-7163.MCT-15-0566 |
0.103 |
|
| 2006 |
Sauvé Y, Karan G, Yang Z, Li C, Hu J, Zhang K. Treatment with carbonic anhydrase inhibitors depresses electroretinogram responsiveness in mice. Advances in Experimental Medicine and Biology. 572: 439-46. PMID 17249607 DOI: 10.1007/0-387-32442-9_61 |
0.094 |
|
| 2004 |
Maugeri A, Meire F, Hoyng CB, Vink C, Van Regemorter N, Karan G, Yang Z, Cremers FP, Zhang K. A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy. Investigative Ophthalmology & Visual Science. 45: 4263-7. PMID 15557430 DOI: 10.1167/Iovs.04-0078 |
0.088 |
|
| 1991 |
Hai AA, Singh A, Mittal VK, Karan GC. Amoebic liver abscess. Review of 220 cases. International Surgery. 76: 81-3. PMID 1869393 |
0.087 |
|
| 2016 |
Karan G, Wang H, Chakrabarti A, Karan S, Liu Z, Xia Z, Gundluru M, Moreton S, Saunthararajah Y, Jackson MW, Agarwal MK, Wald DN. Identification of a small molecule that overcomes HdmX-mediated suppression of p53. Molecular Cancer Therapeutics. PMID 26883273 DOI: 10.1158/1535-7163.MCT-15-0467 |
0.082 |
|
| 2008 |
Yang Z, Chen Y, Lillo C, Chien J, Yu Z, Michaelides M, Klein M, Howes KA, Li Y, Kaminoh Y, Chen H, Zhao C, Chen Y, Al-Sheikh YT, Karan G, et al. Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice. The Journal of Clinical Investigation. 118: 2908-16. PMID 18654668 DOI: 10.1172/Jci35891 |
0.082 |
|
| 2008 |
Haldar M, Karan G, Tvrdik P, Capecchi MR. Two cell lineages, myf5 and myf5-independent, participate in mouse skeletal myogenesis. Developmental Cell. 14: 437-45. PMID 18331721 DOI: 10.1016/J.Devcel.2008.01.002 |
0.081 |
|
| 2006 |
Katz BJ, Yang Z, Payne M, Lin Y, Zhao Y, Pearson E, Duan S, Kamaya S, Karan G, Zhang K. Fundus appearance of choroideremia using optical coherence tomograpy. Advances in Experimental Medicine and Biology. 572: 57-61. PMID 17249555 DOI: 10.1007/0-387-32442-9_9 |
0.081 |
|
| 2016 |
Shelar SB, Narasimhan M, Shanmugam G, Litovsky SH, Gounder SS, Karan G, Arulvasu C, Kensler TW, Hoidal JR, Darley-Usmar VM, Rajasekaran NS. Disruption of nuclear factor (erythroid-derived-2)-like 2 antioxidant signaling: a mechanism for impaired activation of stem cells and delayed regeneration of skeletal muscle. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 26839378 DOI: 10.1096/Fj.201500153 |
0.075 |
|
| 2014 |
Haldar M, Karan G, Watanabe S, Guenther S, Braun T, Capecchi MR. Response: Contributions of the Myf5-independent lineage to myogenesis. Developmental Cell. 31: 539-41. PMID 25490265 DOI: 10.1016/J.Devcel.2014.11.010 |
0.071 |
|
| 2004 |
Berry V, Yang Z, Addison PK, Francis PJ, Ionides A, Karan G, Jiang L, Lin W, Hu J, Yang R, Moore A, Zhang K, Bhattacharya SS. Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4). Journal of Medical Genetics. 41: e109. PMID 15286169 DOI: 10.1136/jmg.2004.020289 |
0.064 |
|
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