| Year |
Citation |
Score |
| 2022 |
Moreno-Leon L, Quezada-Ramirez MA, Bilsbury E, Kiss C, Guerin A, Khanna H. Prenatal phenotype analysis and mutation identification of a fetus with meckel gruber syndrome. Frontiers in Genetics. 13: 982127. PMID 36061204 DOI: 10.3389/fgene.2022.982127 |
0.338 |
|
| 2020 |
Moreno-Leon L, West EL, O'Hara-Wright M, Li L, Nair R, He J, Anand M, Sahu B, Chavali VRM, Smith AJ, Ali RR, Jacobson SG, Cideciyan AV, Khanna H. RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP). Human Molecular Genetics. PMID 33355362 DOI: 10.1093/hmg/ddaa269 |
0.344 |
|
| 2020 |
Vishwakarma S, Gupta RK, Jakati S, Tyagi M, Pappuru RR, Reddig K, Hendricks G, Volkert MR, Khanna H, Chhablani J, Kaur I. Molecular Assessment of Epiretinal Membrane: Activated Microglia, Oxidative Stress and Inflammation. Antioxidants (Basel, Switzerland). 9. PMID 32717933 DOI: 10.3390/Antiox9080654 |
0.357 |
|
| 2019 |
Li L, Rao KN, Khanna H. Structural but Not Functional Alterations in Cones in the Absence of the Retinal Disease Protein Retinitis Pigmentosa 2 (RP2) in a Cone-Only Retina. Frontiers in Genetics. 10: 323. PMID 31024631 DOI: 10.3389/Fgene.2019.00323 |
0.469 |
|
| 2018 |
Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A. Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration. Human Molecular Genetics. PMID 30285110 DOI: 10.1093/hmg/ddy342 |
0.334 |
|
| 2018 |
Shivanna M, Anand M, Chakrabarti S, Khanna H. Ocular Ciliopathies: genetic and mechanistic insights into developing therapies. Current Medicinal Chemistry. PMID 30221600 DOI: 10.2174/0929867325666180917102557 |
0.429 |
|
| 2018 |
Schlegel J, Hoffmann J, Röll D, Müller B, Günther S, Zhang W, Janise A, Vössing C, Fühler B, Neidhardt J, Khanna H, Lorenz B, Stieger K. Toward genome editing in X-linked RP-development of a mouse model with specific treatment relevant features. Translational Research : the Journal of Laboratory and Clinical Medicine. PMID 30213530 DOI: 10.1016/J.Trsl.2018.08.006 |
0.441 |
|
| 2018 |
Khanna H. More Than Meets the Eye: Current Understanding of RPGR Function. Advances in Experimental Medicine and Biology. 1074: 521-538. PMID 29721984 DOI: 10.1007/978-3-319-75402-4_64 |
0.52 |
|
| 2017 |
Megaw R, Abu-Arafeh H, Jungnickel M, Mellough C, Gurniak C, Witke W, Zhang W, Khanna H, Mill P, Dhillon B, Wright AF, Lako M, Ffrench-Constant C. Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models. Nature Communications. 8: 271. PMID 28814713 DOI: 10.1038/S41467-017-00111-8 |
0.515 |
|
| 2017 |
Zhang W, Li L, Su Q, Gao G, Khanna H. Gene therapy using a miniCEP290 fragment delays photoreceptor degeneration in a mouse model of Leber congenital amaurosis (LCA). Human Gene Therapy. PMID 28679290 DOI: 10.1089/Hum.2017.049 |
0.472 |
|
| 2017 |
Kabra M, Zhang W, Rathi S, Mandal AK, Senthil S, Pyatla G, Ramappa M, Banerjee S, Shekhar K, Marmamula S, Mettla AL, Kaur I, Khanna RC, Khanna H, Chakrabarti S. Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma. Human Genetics. PMID 28620713 DOI: 10.1007/S00439-017-1823-6 |
0.345 |
|
| 2016 |
Rao KN, Zhang W, Li L, Anand M, Khanna H. Prenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert syndrome-associated protein INPP5E. Human Molecular Genetics. 25: 4533-4545. PMID 28172980 DOI: 10.1093/Hmg/Ddw281 |
0.471 |
|
| 2016 |
Li L, Khanna H. Stem cells with a view: a look inside a retinal ciliopathy. Stem Cell Investigation. 3: 62. PMID 27868044 DOI: 10.21037/Sci.2016.09.19 |
0.322 |
|
| 2016 |
Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A. Variegated yet Non-Random Rod and Cone Photoreceptor Disease Patterns in RPGR-ORF15-associated Retinal Degeneration. Human Molecular Genetics. PMID 27798110 DOI: 10.1093/Hmg/Ddw361 |
0.506 |
|
| 2016 |
Rao KN, Zhang W, Li L, Anand M, Khanna H. Prenylated retinal ciliopathy protein RPGR interacts with PDE6δ and regulates ciliary localization of Joubert Syndrome-associated protein INPP5E. Human Molecular Genetics. PMID 27554114 DOI: 10.1093/hmg/ddw281 |
0.379 |
|
| 2016 |
Petit L, Khanna H, Punzo C. Advances In Gene Therapy For Diseases Of The Eye. Human Gene Therapy. PMID 27178388 DOI: 10.1089/Hum.2016.040 |
0.326 |
|
| 2016 |
Rao KN, Anand M, Khanna H. The carboxyl terminal mutational hotspot of the ciliary disease protein RPGRORF15 (retinitis pigmentosa GTPase regulator) is glutamylated in vivo. Biology Open. PMID 26941104 DOI: 10.1242/Bio.016816 |
0.444 |
|
| 2016 |
Rao KN, Zhang W, Li L, Ronquillo C, Baehr W, Khanna H. Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR. Human Molecular Genetics. PMID 26936822 DOI: 10.1093/Hmg/Ddw075 |
0.494 |
|
| 2016 |
Rao KN, Li L, Zhang W, Brush RS, Rajala RV, Khanna H. Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina. Human Molecular Genetics. PMID 26908598 DOI: 10.1093/Hmg/Ddw017 |
0.487 |
|
| 2015 |
Khanna H. Photoreceptor Sensory Cilium: Traversing the Ciliary Gate. Cells. 4: 674-86. PMID 26501325 DOI: 10.3390/Cells4040674 |
0.403 |
|
| 2015 |
Li L, Rao KN, Zheng-Le Y, Hurd TW, Lillo C, Khanna H. Loss of Retinitis Pigmentosa 2 (RP2) protein affects cone photoreceptor sensory cilium elongation in mice. Cytoskeleton (Hoboken, N.J.). PMID 26383048 DOI: 10.1002/Cm.21255 |
0.519 |
|
| 2015 |
Mookherjee S, Hiriyanna S, Kaneshiro K, Li L, Li Y, Li W, Qian H, Li T, Khanna H, Colosi P, Swaroop A, Wu Z. Long-Term Rescue of Cone Photoreceptor Degeneration in Retinitis Pigmentosa 2 (RP2) Knockout Mice by Gene Replacement Therapy. Human Molecular Genetics. PMID 26358772 DOI: 10.1093/Hmg/Ddv354 |
0.462 |
|
| 2015 |
Rao KN, Li L, Anand M, Khanna H. Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition. Scientific Reports. 5: 11137. PMID 26068394 DOI: 10.1038/Srep11137 |
0.502 |
|
| 2015 |
Li L, Anand M, Rao KN, Khanna H. Cilia in photoreceptors. Methods in Cell Biology. 127: 75-92. PMID 25837387 DOI: 10.1016/Bs.Mcb.2014.12.005 |
0.458 |
|
| 2015 |
Rao KN, Li L, Anand M, Khanna H. Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition Scientific Reports. 5. DOI: 10.1038/srep11137 |
0.361 |
|
| 2015 |
Mookherjee S, Hiriyanna S, Kaneshiro K, Qian H, Li T, Khanna H, Colosi P, Swaroop A, Wu Z. 714. Gene Therapy Rescues Cone Function and Viability in an Rp2 Knockout Mouse Model for X-Linked Retinitis Pigmentosa Over a Wide Dose Range and a Broad Therapeutic Time Window Molecular Therapy. 23: S285. DOI: 10.1016/S1525-0016(16)34323-4 |
0.46 |
|
| 2014 |
Subramanian B, Anand M, Khan NW, Khanna H. Loss of Raf-1 kinase inhibitory protein delays early-onset severe retinal ciliopathy in Cep290rd16 mouse. Investigative Ophthalmology & Visual Science. 55: 5788-94. PMID 25125607 DOI: 10.1167/Iovs.14-14954 |
0.494 |
|
| 2014 |
Subramanian B, Anand M, Khanna H. Ablation Of Raf-1 Kinase Inhibitory Protein (RKIP) Improves Photoreceptor Structure and Function in a Cep290-Mutant Mouse Model Of Severe Retinal Degeneration Investigative Ophthalmology & Visual Science. 55: 6317-6317. DOI: 10.13028/702Y-Q067 |
0.452 |
|
| 2013 |
Li L, Khan N, Hurd T, Ghosh AK, Cheng C, Molday R, Heckenlively JR, Swaroop A, Khanna H. Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 54: 4503-11. PMID 23745007 DOI: 10.1167/Iovs.13-12140 |
0.501 |
|
| 2013 |
Khanna H. New mechanisms and treatment modalities for retinal degenerative diseases Journal of Clinical & Experimental Ophthalmology. DOI: 10.4172/2155-9570.S1.010 |
0.438 |
|
| 2012 |
Servattalab S, Yildiz O, Khanna H. Tackling Primary Cilia Dysfunction in Photoreceptor Degenerative Diseases of the Eye. International Journal of Ophthalmic Pathology. 1. PMID 24455751 DOI: 10.4172/2324-8599.1000E101 |
0.383 |
|
| 2012 |
Khanna H, Baehr W. Retina ciliopathies: from genes to mechanisms and treatment. Vision Research. 75: 1. PMID 23206575 DOI: 10.1016/J.Visres.2012.11.007 |
0.333 |
|
| 2012 |
Yildiz O, Khanna H. Ciliary signaling cascades in photoreceptors. Vision Research. 75: 112-6. PMID 22921640 DOI: 10.1016/J.Visres.2012.08.007 |
0.349 |
|
| 2012 |
Anand M, Khanna H. Ciliary transition zone (TZ) proteins RPGR and CEP290: role in photoreceptor cilia and degenerative diseases. Expert Opinion On Therapeutic Targets. 16: 541-51. PMID 22563985 DOI: 10.1517/14728222.2012.680956 |
0.332 |
|
| 2012 |
Thompson DA, Khan NW, Othman MI, Chang B, Jia L, Grahek G, Wu Z, Hiriyanna S, Nellissery J, Li T, Khanna H, Colosi P, Swaroop A, Heckenlively JR. Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15. Plos One. 7: e35865. PMID 22563472 DOI: 10.1371/Journal.Pone.0035865 |
0.521 |
|
| 2012 |
Luo N, West CC, Murga-Zamalloa CA, Sun L, Anderson RM, Wells CD, Weinreb RN, Travers JB, Khanna H, Sun Y. OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome. Human Molecular Genetics. 21: 3333-44. PMID 22543976 DOI: 10.1093/Hmg/Dds163 |
0.397 |
|
| 2012 |
Rachel RA, May-Simera HL, Veleri S, Gotoh N, Choi BY, Murga-Zamalloa C, McIntyre JC, Marek J, Lopez I, Hackett AN, Zhang J, Brooks M, den Hollander AI, Beales PL, Li T, ... ... Khanna H, et al. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. The Journal of Clinical Investigation. 122: 1233-45. PMID 22446187 DOI: 10.1172/Jci60981 |
0.463 |
|
| 2012 |
Beltran WA, Cideciyan AV, Lewin AS, Iwabe S, Khanna H, Sumaroka A, Chiodo VA, Fajardo DS, Román AJ, Deng WT, Swider M, Alemán TS, Boye SL, Genini S, Swaroop A, et al. Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa. Proceedings of the National Academy of Sciences of the United States of America. 109: 2132-7. PMID 22308428 DOI: 10.1073/Pnas.1118847109 |
0.502 |
|
| 2011 |
Bian ZM, Elner SG, Khanna H, Murga-Zamalloa CA, Patil S, Elner VM. Expression and functional roles of caspase-5 in inflammatory responses of human retinal pigment epithelial cells. Investigative Ophthalmology & Visual Science. 52: 8646-56. PMID 21969293 DOI: 10.1167/Iovs.11-7570 |
0.404 |
|
| 2011 |
Patil SB, Hurd TW, Ghosh AK, Murga-Zamalloa CA, Khanna H. Functional analysis of retinitis pigmentosa 2 (RP2) protein reveals variable pathogenic potential of disease-associated missense variants. Plos One. 6: e21379. PMID 21738648 DOI: 10.1371/Journal.Pone.0021379 |
0.538 |
|
| 2011 |
Murga-Zamalloa CA, Ghosh AK, Patil SB, Reed NA, Chan LS, Davuluri S, Peränen J, Hurd TW, Rachel RA, Khanna H. Accumulation of the Raf-1 kinase inhibitory protein (Rkip) is associated with Cep290-mediated photoreceptor degeneration in ciliopathies. The Journal of Biological Chemistry. 286: 28276-86. PMID 21685394 DOI: 10.1074/Jbc.M111.237560 |
0.49 |
|
| 2011 |
Chakarova CF, Khanna H, Shah AZ, Patil SB, Sedmak T, Murga-Zamalloa CA, Papaioannou MG, Nagel-Wolfrum K, Lopez I, Munro P, Cheetham M, Koenekoop RK, Rios RM, Matter K, Wolfrum U, et al. TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein. Human Molecular Genetics. 20: 975-87. PMID 21159800 DOI: 10.1093/Hmg/Ddq543 |
0.541 |
|
| 2011 |
Yao J, Feathers KL, Khanna H, Thompson D, Tsilfidis C, Hauswirth WW, Heckenlively JR, Swaroop A, Zacks DN. XIAP therapy increases survival of transplanted rod precursors in a degenerating host retina. Investigative Ophthalmology & Visual Science. 52: 1567-72. PMID 20926819 DOI: 10.1167/Iovs.10-5998 |
0.321 |
|
| 2010 |
Otto EA, Hurd TW, Airik R, Chaki M, Zhou W, Stoetzel C, Patil SB, Levy S, Ghosh AK, Murga-Zamalloa CA, van Reeuwijk J, Letteboer SJ, Sang L, Giles RH, Liu Q, ... ... Khanna H, et al. Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy. Nature Genetics. 42: 840-50. PMID 20835237 DOI: 10.1038/Ng.662 |
0.419 |
|
| 2010 |
Patil SB, Verma R, Venkatareddy M, Khanna H. Expression and localization of the ciliary disease protein retinitis pigmentosa GTPase regulator in mammalian kidney. Kidney International. 78: 622-3. PMID 20805823 DOI: 10.1038/Ki.2010.252 |
0.456 |
|
| 2010 |
Hurd T, Zhou W, Jenkins P, Liu CJ, Swaroop A, Khanna H, Martens J, Hildebrandt F, Margolis B. The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development. Human Molecular Genetics. 19: 4330-44. PMID 20729296 DOI: 10.1093/Hmg/Ddq355 |
0.474 |
|
| 2010 |
Murga-Zamalloa CA, Desai NJ, Hildebrandt F, Khanna H. Interaction of ciliary disease protein retinitis pigmentosa GTPase regulator with nephronophthisis-associated proteins in mammalian retinas. Molecular Vision. 16: 1373-81. PMID 20664800 |
0.435 |
|
| 2010 |
Murga-Zamalloa CA, Atkins SJ, Peranen J, Swaroop A, Khanna H. Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration. Human Molecular Genetics. 19: 3591-8. PMID 20631154 DOI: 10.1093/Hmg/Ddq275 |
0.539 |
|
| 2010 |
Jayasundera T, Branham KE, Othman M, Rhoades WR, Karoukis AJ, Khanna H, Swaroop A, Heckenlively JR. RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 915-23. PMID 20625056 DOI: 10.1001/Archophthalmol.2010.122 |
0.44 |
|
| 2010 |
Patzke S, Redick S, Warsame A, Murga-Zamalloa CA, Khanna H, Doxsey S, Stokke T. CSPP is a ciliary protein interacting with Nephrocystin 8 and required for cilia formation. Molecular Biology of the Cell. 21: 2555-67. PMID 20519441 DOI: 10.1091/Mbc.E09-06-0503 |
0.421 |
|
| 2010 |
Murga-Zamalloa C, Swaroop A, Khanna H. Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP). Advances in Experimental Medicine and Biology. 664: 105-14. PMID 20238008 DOI: 10.1007/978-1-4419-1399-9_13 |
0.544 |
|
| 2010 |
O'Toole JF, Liu Y, Davis EE, Westlake CJ, Attanasio M, Otto EA, Seelow D, Nurnberg G, Becker C, Nuutinen M, Kärppä M, Ignatius J, Uusimaa J, Pakanen S, Jaakkola E, ... ... Khanna H, et al. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy. The Journal of Clinical Investigation. 120: 791-802. PMID 20179356 DOI: 10.1172/Jci40076 |
0.412 |
|
| 2010 |
Wu DM, Khanna H, Atmaca-Sonmez P, Sieving PA, Branham K, Othman M, Swaroop A, Daiger SP, Heckenlively JR. Long-term follow-up of a family with dominant X-linked retinitis pigmentosa. Eye (London, England). 24: 764-74. PMID 19893586 DOI: 10.1038/Eye.2009.270 |
0.385 |
|
| 2010 |
Ghosh AK, Murga-Zamalloa CA, Chan L, Hitchcock PF, Swaroop A, Khanna H. Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development. Human Molecular Genetics. 19: 90-8. PMID 19815619 DOI: 10.1093/Hmg/Ddp469 |
0.499 |
|
| 2010 |
O'Toole JF, Liu Y, Davis EE, Westlake CJ, Attanasio M, Otto EA, Seelow D, Nurnberg G, Becker C, Nuutinen M, Kärppä M, Ignatius J, Uusimaa J, Pakanen S, Jaakkola E, ... ... Khanna H, et al. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076) Journal of Clinical Investigation. 120: 1362. DOI: 10.1172/Jci40076C1 |
0.326 |
|
| 2009 |
Murga-Zamalloa CA, Swaroop A, Khanna H. RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction. Journal of Genetics. 88: 399-407. PMID 20090203 DOI: 10.1007/S12041-009-0061-7 |
0.49 |
|
| 2009 |
Khanna H, Davis EE, Murga-Zamalloa CA, Estrada-Cuzcano A, Lopez I, den Hollander AI, Zonneveld MN, Othman MI, Waseem N, Chakarova CF, Maubaret C, Diaz-Font A, MacDonald I, Muzny DM, Wheeler DA, et al. A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nature Genetics. 41: 739-45. PMID 19430481 DOI: 10.1038/Ng.366 |
0.499 |
|
| 2008 |
Tsang WY, Bossard C, Khanna H, Peränen J, Swaroop A, Malhotra V, Dynlacht BD. CP110 suppresses primary cilia formation through its interaction with CEP290, a protein deficient in human ciliary disease. Developmental Cell. 15: 187-97. PMID 18694559 DOI: 10.1016/J.Devcel.2008.07.004 |
0.39 |
|
| 2008 |
Siffroi-Fernandez S, Felder-Schmittbuhl MP, Khanna H, Swaroop A, Hicks D. FGF19 exhibits neuroprotective effects on adult mammalian photoreceptors in vitro. Investigative Ophthalmology & Visual Science. 49: 1696-704. PMID 18385093 DOI: 10.1167/Iovs.07-1272 |
0.322 |
|
| 2008 |
He S, Parapuram SK, Hurd TW, Behnam B, Margolis B, Swaroop A, Khanna H. Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: insights into X-linked Retinitis Pigmentosa and associated ciliopathies. Vision Research. 48: 366-76. PMID 17904189 DOI: 10.1016/J.Visres.2007.08.005 |
0.534 |
|
| 2007 |
Chakarova CF, Papaioannou MG, Khanna H, Lopez I, Waseem N, Shah A, Theis T, Friedman J, Maubaret C, Bujakowska K, Veraitch B, Abd El-Aziz MM, Prescott de Q, Parapuram SK, Bickmore WA, et al. Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy. American Journal of Human Genetics. 81: 1098-103. PMID 17924349 DOI: 10.1086/521953 |
0.52 |
|
| 2007 |
McEwen DP, Koenekoop RK, Khanna H, Jenkins PM, Lopez I, Swaroop A, Martens JR. Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons. Proceedings of the National Academy of Sciences of the United States of America. 104: 15917-22. PMID 17898177 DOI: 10.1073/Pnas.0704140104 |
0.379 |
|
| 2007 |
Cideciyan AV, Aleman TS, Jacobson SG, Khanna H, Sumaroka A, Aguirre GK, Schwartz SB, Windsor EA, He S, Chang B, Stone EM, Swaroop A. Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis. Human Mutation. 28: 1074-83. PMID 17554762 DOI: 10.1002/Humu.20565 |
0.478 |
|
| 2007 |
Oh EC, Khan N, Novelli E, Khanna H, Strettoi E, Swaroop A. Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL. Proceedings of the National Academy of Sciences of the United States of America. 104: 1679-84. PMID 17242361 DOI: 10.1073/Pnas.0605934104 |
0.442 |
|
| 2006 |
Khanna H, Akimoto M, Siffroi-Fernandez S, Friedman JS, Hicks D, Swaroop A. Retinoic acid regulates the expression of photoreceptor transcription factor NRL. The Journal of Biological Chemistry. 281: 27327-34. PMID 16854989 DOI: 10.1074/Jbc.M605500200 |
0.322 |
|
| 2006 |
Sayer JA, Otto EA, O'Toole JF, Nurnberg G, Kennedy MA, Becker C, Hennies HC, Helou J, Attanasio M, Fausett BV, Utsch B, Khanna H, Liu Y, Drummond I, Kawakami I, et al. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature Genetics. 38: 674-81. PMID 16682973 DOI: 10.1038/Ng1786 |
0.454 |
|
| 2006 |
Chang B, Khanna H, Hawes N, Jimeno D, He S, Lillo C, Parapuram SK, Cheng H, Scott A, Hurd RE, Sayer JA, Otto EA, Attanasio M, O'Toole JF, Jin G, et al. In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse. Human Molecular Genetics. 15: 1847-57. PMID 16632484 DOI: 10.1093/Hmg/Ddl107 |
0.519 |
|
| 2005 |
Khanna H, Hurd TW, Lillo C, Shu X, Parapuram SK, He S, Akimoto M, Wright AF, Margolis B, Williams DS, Swaroop A. RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins. The Journal of Biological Chemistry. 280: 33580-7. PMID 16043481 DOI: 10.1074/Jbc.M505827200 |
0.513 |
|
| 2005 |
Shu X, Fry AM, Tulloch B, Manson FD, Crabb JW, Khanna H, Faragher AJ, Lennon A, He S, Trojan P, Giessl A, Wolfrum U, Vervoort R, Swaroop A, Wright AF. RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin. Human Molecular Genetics. 14: 1183-97. PMID 15772089 DOI: 10.1093/Hmg/Ddi129 |
0.399 |
|
| 2005 |
Otto EA, Loeys B, Khanna H, Hellemans J, Sudbrak R, Fan S, Muerb U, O'Toole JF, Helou J, Attanasio M, Utsch B, Sayer JA, Lillo C, Jimeno D, Coucke P, et al. Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin. Nature Genetics. 37: 282-8. PMID 15723066 DOI: 10.1038/Ng1520 |
0.518 |
|
| 2004 |
Friedman JS, Khanna H, Swain PK, Denicola R, Cheng H, Mitton KP, Weber CH, Hicks D, Swaroop A. The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding protein. The Journal of Biological Chemistry. 279: 47233-41. PMID 15328344 DOI: 10.1074/Jbc.M408298200 |
0.362 |
|
| 2004 |
Cheng H, Khanna H, Oh EC, Hicks D, Mitton KP, Swaroop A. Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors. Human Molecular Genetics. 13: 1563-75. PMID 15190009 DOI: 10.1093/Hmg/Ddh173 |
0.473 |
|
| 2003 |
Mitton KP, Swain PK, Khanna H, Dowd M, Apel IJ, Swaroop A. Interaction of retinal bZIP transcription factor NRL with Flt3-interacting zinc-finger protein Fiz1: possible role of Fiz1 as a transcriptional repressor. Human Molecular Genetics. 12: 365-73. PMID 12566383 DOI: 10.1093/Hmg/Ddg035 |
0.481 |
|
| 1998 |
Xu T, Khanna H, Coward JK. The design, synthesis, and initial evaluation of benzophenone-containing peptides as potential photoaffinity labels of oligosaccharyltransferase. Bioorganic & Medicinal Chemistry. 6: 1821-34. PMID 9839012 DOI: 10.1016/S0968-0896(98)00135-7 |
0.553 |
|
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