Graeme Mardon - Publications

Affiliations: 
Baylor College of Medicine, Houston, TX 
Area:
Drosophila and Vertebrate eye development

83 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
2018 Yeung K, Wang F, Li Y, Wang K, Mardon G, Chen R. Integrative genomic analysis reveals novel regulatory mechanisms of eyeless during Drosophila eye development. Nucleic Acids Research. PMID 30295802 DOI: 10.1093/nar/gky892  0.96
2018 Yin W, Kim HT, Wang S, Gunawan F, Wang L, Kishimoto K, Zhong H, Roman D, Preussner J, Guenther S, Graef V, Buettner C, Grohmann B, Looso M, Morimoto M, ... Mardon G, et al. The potassium channel KCNJ13 is essential for smooth muscle cytoskeletal organization during mouse tracheal tubulogenesis. Nature Communications. 9: 2815. PMID 30022023 DOI: 10.1038/s41467-018-05043-5  0.6
2018 Roman D, Zhong H, Yaklichkin S, Chen R, Mardon G. Conditional loss of Kcnj13 in the retinal pigment epithelium causes photoreceptor degeneration. Experimental Eye Research. PMID 30009826 DOI: 10.1016/j.exer.2018.07.014  0.96
2018 Dharmat R, Eblimit A, Robichaux MA, Zhang Z, Nguyen TT, Jung SY, He F, Jain A, Li Y, Qin J, Overbeek P, Roepman R, Mardon G, Wensel TG, Chen R. SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium. The Journal of Cell Biology. PMID 29899041 DOI: 10.1083/jcb.201712117  0.96
2018 Eblimit A, Zaneveld SA, Liu W, Thomas K, Wang K, Li Y, Mardon G, Chen R. NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Experimental Eye Research. PMID 29674119 DOI: 10.1016/j.exer.2018.04.010  0.96
2018 McClard CK, Kochukov MY, Herman I, Liu Z, Eblimit A, Moayedi Y, Ortiz-Guzman J, Colchado D, Pekarek B, Paneerselvam S, Mardon G, Arenkiel BR. POU6f1 Mediates Neuropeptide-Dependent Plasticity in the Adult Brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29305536 DOI: 10.1523/JNEUROSCI.1641-17.2017  0.56
2017 Eblimit A, Agrawal S, Thomas K, Anastassov IA, Tajiguli A, Mardon G, Chen R. Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice. Experimental Eye Research. PMID 29100828 DOI: 10.1016/j.exer.2017.10.015  0.96
2016 Jin M, Eblimit A, Pulikkathara M, Corr S, Chen R, Mardon G. Conditional knockout of retinal determination genes in differentiating cells in Drosophila. The Febs Journal. PMID 27257739 DOI: 10.1111/febs.13772  1
2016 Jin M, Aibar S, Ge Z, Chen R, Aerts S, Mardon G. Identification of Novel Direct Targets of Drosophila Sine Oculis by Integration of Genome-wide Data Sets. Developmental Biology. PMID 27178668 DOI: 10.1016/j.ydbio.2016.05.007  1
2016 Iyer J, Wang Q, Le T, Pizzo L, Grönke S, Ambegaokar S, Imai Y, Srivastava A, Llamusí Troisí B, Mardon G, Artero R, Jackson GR, Isaacs AM, Partridge L, Kumar JP, et al. Quantitative Assessment of Eye Phenotypes for Functional Genetic Studies Using Drosophila melanogaster. G3 (Bethesda, Md.). PMID 26994292 DOI: 10.1534/g3.116.027060  1
2016 Jin M, Mardon G. Distinct Biochemical Activities of Eyes absent During Drosophila Eye Development. Scientific Reports. 6: 23228. PMID 26980695 DOI: 10.1038/srep23228  0.56
2016 Yang Z, Zhong H, Chen J, Zhang X, Zhang H, Luo X, Xu S, Chen H, Lu D, Han Y, Li J, Fu L, Qi X, Peng Y, Xiang K, ... ... Mardon G, et al. A genetic mechanism for convergent skin lightening during recent human evolution. Molecular Biology and Evolution. PMID 26744415 DOI: 10.1093/molbev/msw003  1
2015 Zhong H, Chen Y, Li Y, Chen R, Mardon G. Erratum: CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes. Scientific Reports. 5: 9731. PMID 26177189 DOI: 10.1038/srep09731  0.96
2015 Zhong H, Eblimit A, Moayedi Y, Boye SL, Chiodo VA, Chen Y, Li Y, Nichols RM, Hauswirth WW, Chen R, Mardon G. AAV8(Y733F)-mediated gene therapy in a Spata7 knockout mouse model of Leber congenital amaurosis and retinitis pigmentosa. Gene Therapy. PMID 25965394 DOI: 10.1038/gt.2015.42  1
2015 Chen K, Wu K, Jiao X, Wang L, Ju X, Wang M, Di Sante G, Xu S, Wang Q, Li K, Sun X, Xu C, Li Z, Casimiro MC, Ertel A, ... ... Mardon G, et al. The Endogenous Cell-Fate Factor Dachshund Restrains Prostate Epithelial Cell Migration via Repression of Cytokine Secretion via a CXCL Signaling Module. Cancer Research. 75: 1992-2004. PMID 25769723 DOI: 10.1158/0008-5472.CAN-14-0611  1
2015 Zhong H, Chen Y, Li Y, Chen R, Mardon G. CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes. Scientific Reports. 5: 8366. PMID 25666713 DOI: 10.1038/srep08366  1
2015 Eblimit A, Nguyen TM, Chen Y, Esteve-Rudd J, Zhong H, Letteboer S, Van Reeuwijk J, Simons DL, Ding Q, Wu KM, Li Y, Van Beersum S, Moayedi Y, Xu H, Pickard P, ... ... Mardon G, et al. Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina. Human Molecular Genetics. 24: 1584-601. PMID 25398945 DOI: 10.1093/hmg/ddu573  1
2014 Jusiak B, Wang F, Karandikar UC, Kwak SJ, Wang H, Chen R, Mardon G. Genome-wide DNA binding pattern of the homeodomain transcription factor Sine oculis (So) in the developing eye of Drosophila melanogaster. Genomics Data. 2: 153-155. PMID 25126519 DOI: 10.1016/j.gdata.2014.06.016  1
2014 Karandikar UC, Jin M, Jusiak B, Kwak S, Chen R, Mardon G. Drosophila eyes absent is required for normal cone and pigment cell development. Plos One. 9: e102143. PMID 25057928 DOI: 10.1371/journal.pone.0102143  1
2014 Jusiak B, Karandikar UC, Kwak SJ, Wang F, Wang H, Chen R, Mardon G. Regulation of Drosophila eye development by the transcription factor Sine oculis. Plos One. 9: e89695. PMID 24586968 DOI: 10.1371/journal.pone.0089695  1
2014 Moayedi Y, Basch ML, Pacheco NL, Gao SS, Wang R, Harrison W, Xiao N, Oghalai JS, Overbeek PA, Mardon G, Groves AK. The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organs. Plos Genetics. 10: e1004055. PMID 24391519 DOI: 10.1371/journal.pgen.1004055  1
2013 Atkins M, Jiang Y, Sansores-Garcia L, Jusiak B, Halder G, Mardon G. Dynamic rewiring of the Drosophila retinal determination network switches its function from selector to differentiation. Plos Genetics. 9: e1003731. PMID 24009524 DOI: 10.1371/journal.pgen.1003731  1
2013 Li Y, Jiang Y, Chen Y, Karandikar U, Hoffman K, Chattopadhyay A, Mardon G, Chen R. optix functions as a link between the retinal determination network and the dpp pathway to control morphogenetic furrow progression in Drosophila. Developmental Biology. 381: 50-61. PMID 23792115 DOI: 10.1016/j.ydbio.2013.06.015  1
2013 Haase Gilbert E, Kwak SJ, Chen R, Mardon G. Drosophila signal peptidase complex member Spase12 is required for development and cell differentiation. Plos One. 8: e60908. PMID 23573290 DOI: 10.1371/journal.pone.0060908  1
2013 Jin M, Jusiak B, Bai Z, Mardon G. Eyes absent tyrosine phosphatase activity is not required for Drosophila development or survival. Plos One. 8: e58818. PMID 23554934 DOI: 10.1371/journal.pone.0058818  1
2012 Jusiak B, Abulimiti A, Haelterman N, Chen R, Mardon G. MAPK target sites of eyes absent are not required for eye development or survival in Drosophila. Plos One. 7: e50776. PMID 23251383 DOI: 10.1371/journal.pone.0050776  1
2012 Koenekoop RK, Wang H, Majewski J, Wang X, Lopez I, Ren H, Chen Y, Li Y, Fishman GA, Genead M, Schwartzentruber J, Solanki N, Traboulsi EI, Cheng J, Logan CV, ... ... Mardon G, et al. Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. Nature Genetics. 44: 1035-9. PMID 22842230 DOI: 10.1038/ng.2356  1
2011 Wang H, Chen X, Dudinsky L, Patenia C, Chen Y, Li Y, Wei Y, Abboud EB, Al-Rajhi AA, Lewis RA, Lupski JR, Mardon G, Gibbs RA, Perkins BD, Chen R. Exome capture sequencing identifies a novel mutation in BBS4. Molecular Vision. 17: 3529-40. PMID 22219648  1
2011 Wang X, Wang H, Cao M, Li Z, Chen X, Patenia C, Gore A, Abboud EB, Al-Rajhi AA, Lewis RA, Lupski JR, Mardon G, Zhang K, Muzny D, Gibbs RA, et al. Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis. Human Mutation. 32: 1450-9. PMID 21901789 DOI: 10.1002/humu.21587  1
2011 Anderson AE, Karandikar UC, Pepple KL, Chen Z, Bergmann A, Mardon G. The enhancer of trithorax and polycomb gene Caf1/p55 is essential for cell survival and patterning in Drosophila development. Development (Cambridge, England). 138: 1957-66. PMID 21490066 DOI: 10.1242/dev.058461  1
2011 Jiang Y, Scott KL, Kwak SJ, Chen R, Mardon G. Sds22/PP1 links epithelial integrity and tumor suppression via regulation of myosin II and JNK signaling. Oncogene. 30: 3248-60. PMID 21399659 DOI: 10.1038/onc.2011.46  1
2011 Wiszniewski W, Lewis RA, Stockton DW, Peng J, Mardon G, Chen R, Lupski JR. Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis. Human Genetics. 129: 319-27. PMID 21153841 DOI: 10.1007/s00439-010-0928-y  1
2010 Popov VM, Wu K, Zhou J, Powell MJ, Mardon G, Wang C, Pestell RG. The Dachshund gene in development and hormone-responsive tumorigenesis. Trends in Endocrinology and Metabolism: Tem. 21: 41-9. PMID 19896866 DOI: 10.1016/j.tem.2009.08.002  1
2010 Wang H, den Hollander AI, Moayedi Y, Abulimiti A, Li Y, Collin RWJ, Hoyng CB, Lopez I, Abboud EB, Al-Rajhi AA, Bray M, Lewis RA, Lupski JR, Mardon G, Koenekoop RK, et al. Mutations in SPATA7 Cause Leber Congenital Amaurosis and Juvenile Retinitis Pigmentosa (DOI:10.1016/j.ajhg.2009.02.005) American Journal of Human Genetics. 86: 293. DOI: 10.1016/j.ajhg.2010.01.002  1
2009 Atkins M, Mardon G. Signaling in the third dimension: the peripodial epithelium in eye disc development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 2139-48. PMID 19623613 DOI: 10.1002/dvdy.22034  1
2009 Wang H, den Hollander AI, Moayedi Y, Abulimiti A, Li Y, Collin RW, Hoyng CB, Lopez I, Abboud EB, Al-Rajhi AA, Bray M, Lewis RA, Lupski JR, Mardon G, Koenekoop RK, et al. Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. American Journal of Human Genetics. 84: 380-7. PMID 19268277 DOI: 10.1016/j.ajhg.2009.02.005  1
2009 Li Y, Wang H, Peng J, Gibbs RA, Lewis RA, Lupski JR, Mardon G, Chen R. Mutation survey of known LCA genes and loci in the Saudi Arabian population. Investigative Ophthalmology & Visual Science. 50: 1336-43. PMID 18936139 DOI: 10.1167/iovs.08-2589  1
2008 Pepple KL, Atkins M, Venken K, Wellnitz K, Harding M, Frankfort B, Mardon G. Two-step selection of a single R8 photoreceptor: a bistable loop between senseless and rough locks in R8 fate. Development (Cambridge, England). 135: 4071-9. PMID 19004852 DOI: 10.1242/dev.028951  1
2008 Davis RJ, Harding M, Moayedi Y, Mardon G. Mouse Dach1 and Dach2 are redundantly required for Müllerian duct development. Genesis (New York, N.Y. : 2000). 46: 205-13. PMID 18395837 DOI: 10.1002/dvg.20385  1
2007 Pepple KL, Anderson AE, Frankfort BJ, Mardon G. A genetic screen in Drosophila for genes interacting with senseless during neuronal development identifies the importin moleskin. Genetics. 175: 125-41. PMID 17110483 DOI: 10.1534/genetics.106.065680  1
2006 Ostrin EJ, Li Y, Hoffman K, Liu J, Wang K, Zhang L, Mardon G, Chen R. Genome-wide identification of direct targets of the Drosophila retinal determination protein Eyeless. Genome Research. 16: 466-76. PMID 16533912 DOI: 10.1101/gr.4673006  1
2006 Davis RJ, Pesah YI, Harding M, Paylor R, Mardon G. Mouse Dach2 mutants do not exhibit gross defects in eye development or brain function. Genesis (New York, N.Y. : 2000). 44: 84-92. PMID 16470613 DOI: 10.1002/gene.20188  1
2005 Purcell P, Oliver G, Mardon G, Donner AL, Maas RL. Pax6-dependence of Six3, Eya1 and Dach1 expression during lens and nasal placode induction. Gene Expression Patterns : Gep. 6: 110-8. PMID 16024294 DOI: 10.1016/j.modgep.2005.04.010  1
2005 Pappu KS, Ostrin EJ, Middlebrooks BW, Sili BT, Chen R, Atkins MR, Gibbs R, Mardon G. Dual regulation and redundant function of two eye-specific enhancers of the Drosophila retinal determination gene dachshund. Development (Cambridge, England). 132: 2895-905. PMID 15930118 DOI: 10.1242/dev.01869  1
2005 Chen R, Mardon G. Keeping an eye on the fly genome. Developmental Biology. 282: 285-93. PMID 15893305 DOI: 10.1016/j.ydbio.2005.04.015  1
2005 Pesah Y, Burgess H, Middlebrooks B, Ronningen K, Prosser J, Tirunagaru V, Zysk J, Mardon G. Whole-mount analysis reveals normal numbers of dopaminergic neurons following misexpression of alpha-Synuclein in Drosophila. Genesis (New York, N.Y. : 2000). 41: 154-9. PMID 15789427 DOI: 10.1002/gene.20106  1
2004 Pappu KS, Mardon G. Genetic control of retinal specification and determination in Drosophila. The International Journal of Developmental Biology. 48: 913-24. PMID 15558482 DOI: 10.1387/ijdb.041875kp  1
2004 Domingos PM, Brown S, Barrio R, Ratnakumar K, Frankfort BJ, Mardon G, Steller H, Mollereau B. Regulation of R7 and R8 differentiation by the spalt genes. Developmental Biology. 273: 121-33. PMID 15302602 DOI: 10.1016/j.ydbio.2004.05.026  1
2004 Tavsanli BC, Ostrin EJ, Burgess HK, Middlebrooks BW, Pham TA, Mardon G. Structure-function analysis of the Drosophila retinal determination protein Dachshund. Developmental Biology. 272: 231-47. PMID 15242803 DOI: 10.1016/j.ydbio.2004.05.005  1
2004 Frankfort BJ, Pepple KL, Mamlouk M, Rose MF, Mardon G. Senseless is required for pupal retinal development in Drosophila. Genesis (New York, N.Y. : 2000). 38: 182-94. PMID 15083519 DOI: 10.1002/gene.20018  1
2004 Pesah Y, Pham T, Burgess H, Middlebrooks B, Verstreken P, Zhou Y, Harding M, Bellen H, Mardon G. Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress. Development (Cambridge, England). 131: 2183-94. PMID 15073152 DOI: 10.1242/dev.01095  1
2004 Frankfort BJ, Mardon G. Senseless represses nuclear transduction of Egfr pathway activation. Development (Cambridge, England). 131: 563-70. PMID 14711872 DOI: 10.1242/dev.00941  1
2003 Rayapureddi JP, Kattamuri C, Steinmetz BD, Frankfort BJ, Ostrin EJ, Mardon G, Hegde RS. Eyes absent represents a class of protein tyrosine phosphatases. Nature. 426: 295-8. PMID 14628052 DOI: 10.1038/nature02093  1
2003 Davis RJ, Tavsanli BC, Dittrich C, Walldorf U, Mardon G. Drosophila retinal homeobox (drx) is not required for establishment of the visual system, but is required for brain and clypeus development. Developmental Biology. 259: 272-87. PMID 12871701 DOI: 10.1016/S0012-1606(03)00201-X  1
2003 Pappu KS, Chen R, Middlebrooks BW, Woo C, Heberlein U, Mardon G. Mechanism of hedgehog signaling during Drosophila eye development. Development (Cambridge, England). 130: 3053-62. PMID 12756186 DOI: 10.1242/dev.00534  1
2002 Pappu K, Mardon G. Retinal specification and determination in Drosophila. Results and Problems in Cell Differentiation. 37: 5-20. PMID 25707066  1
2002 Inoue Y, Mito T, Miyawaki K, Matsushima K, Shinmyo Y, Heanue TA, Mardon G, Ohuchi H, Noji S. Correlation of expression patterns of homothorax, dachshund, and Distal-less with the proximodistal segmentation of the cricket leg bud. Mechanisms of Development. 113: 141-8. PMID 11960702 DOI: 10.1016/S0925-4773(02)00017-5  1
2002 Frankfort BJ, Mardon G. R8 development in the Drosophila eye: a paradigm for neural selection and differentiation. Development (Cambridge, England). 129: 1295-306. PMID 11880339  1
2002 Loosli F, Mardon G, Wittbrodt J. Cloning and expression of medaka Dachshund. Mechanisms of Development. 112: 203-6. PMID 11850196 DOI: 10.1016/S0925-4773(01)00649-9  1
2002 Heanue TA, Davis RJ, Rowitch DH, Kispert A, McMahon AP, Mardon G, Tabin CJ. Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes. Mechanisms of Development. 111: 75-87. PMID 11804780 DOI: 10.1016/S0925-4773(01)00611-6  1
2001 Tavsanli BC, Pappu KS, Mehta SQ, Mardon G. Dbest1, a Drosophila homolog of human Bestrophin, is not required for viability or photoreceptor integrity. Genesis (New York, N.Y. : 2000). 31: 130-6. PMID 11747204 DOI: 10.1002/gene.10013  1
2001 Tavsanli BC, Pappu KS, Mehta SQ, Mardon G. Removal of the floxed neo gene from a conditional knockout allele by the adenoviral Cre recombinase in vivo Genesis. 31: 126-129. PMID 11747203 DOI: 10.1002/gene.10015  1
2001 Frankfort BJ, Nolo R, Zhang Z, Bellen H, Mardon G. senseless repression of rough is required for R8 photoreceptor differentiation in the developing Drosophila eye. Neuron. 32: 403-14. PMID 11709152 DOI: 10.1016/S0896-6273(01)00480-9  1
2001 Davis RJ, Shen W, Sandler YI, Heanue TA, Mardon G. Characterization of mouse Dach2, a homologue of Drosophila dachshund. Mechanisms of Development. 102: 169-79. PMID 11287190 DOI: 10.1016/S0925-4773(01)00307-0  1
2001 Davis RJ, Shen W, Sandler YI, Amoui M, Purcell P, Maas R, Ou CN, Vogel H, Beaudet AL, Mardon G. Dach1 mutant mice bear no gross abnormalities in eye, limb, and brain development and exhibit postnatal lethality. Molecular and Cellular Biology. 21: 1484-90. PMID 11238885 DOI: 10.1128/MCB.21.5.1484-1490.2001  1
2000 Martini SR, Roman G, Meuser S, Mardon G, Davis RL. The retinal determination gene, dachshund, is required for mushroom body cell differentiation. Development (Cambridge, England). 127: 2663-72. PMID 10821764  1
1999 Heanue TA, Reshef R, Davis RJ, Mardon G, Oliver G, Tomarev S, Lassar AB, Tabin CJ. Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation. Genes & Development. 13: 3231-43. PMID 10617572 DOI: 10.1101/gad.13.24.3231  1
1999 Davis RJ, Shen W, Heanue TA, Mardon G. Mouse Dach, a homologue of Drosophila dachshund, is expressed in the developing retina, brain and limbs. Development Genes and Evolution. 209: 526-36. PMID 10502109 DOI: 10.1007/s004270050285  1
1999 Chen R, Halder G, Zhang Z, Mardon G. Signaling by the TGF-beta homolog decapentaplegic functions reiteratively within the network of genes controlling retinal cell fate determination in Drosophila. Development (Cambridge, England). 126: 935-43. PMID 9927595  1
1997 Chen R, Amoui M, Zhang Z, Mardon G. Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila. Cell. 91: 893-903. PMID 9428513 DOI: 10.1016/S0092-8674(00)80481-X  1
1997 Shen W, Mardon G. Ectopic eye development in Drosophila induced by directed dachshund expression. Development (Cambridge, England). 124: 45-52. PMID 9006066  1
1994 Mardon G, Solomon NM, Rubin GM. dachshund encodes a nuclear protein required for normal eye and leg development in Drosophila. Development (Cambridge, England). 120: 3473-86. PMID 7821215  1
1992 Gaul U, Mardon G, Rubin GM. A putative Ras GTPase activating protein acts as a negative regulator of signaling by the Sevenless receptor tyrosine kinase. Cell. 68: 1007-19. PMID 1547500 DOI: 10.1016/0092-8674(92)90073-L  1
1992 Simon MA, Carthew RW, Fortini ME, Gaul U, Mardon G, Rubin GM. Signal transduction pathway initiated by activation of the sevenless tyrosine kinase receptor. Cold Spring Harbor Symposia On Quantitative Biology. 57: 375-80. PMID 1339672  1
1990 Mardon G, Luoh SW, Simpson EM, Gill G, Brown LG, Page DC. Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers. Molecular and Cellular Biology. 10: 681-8. PMID 2105457  1
1989 Schaeffer E, Smith D, Mardon G, Quinn W, Zuker C. Isolation and characterization of two new drosophila protein kinase C genes, including one specifically expressed in photoreceptor cells. Cell. 57: 403-12. PMID 2720775 DOI: 10.1016/0092-8674(89)90915-X  1
1989 Mardon G, Mosher R, Disteche CM, Nishioka Y, McLaren A, Page DC. Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome. Science (New York, N.Y.). 243: 78-80. PMID 2563173  1
1989 Schneider-Gädicke A, Beer-Romero P, Brown LG, Mardon G, Luoh SW, Page DC. Putative transcription activator with alternative isoforms encoded by human ZFX gene. Nature. 342: 708-11. PMID 2512506 DOI: 10.1038/342708a0  1
1989 Mardon G, Page DC. The sex-determining region of the mouse Y chromosome encodes a protein with a highly acidic domain and 13 zinc fingers. Cell. 56: 765-70. PMID 2493989 DOI: 10.1016/0092-8674(89)90680-6  1
1988 Kaplan JM, Mardon G, Bishop JM, Varmus HE. The first seven amino acids encoded by the v-src oncogene act as a myristylation signal: lysine 7 is a critical determinant. Molecular and Cellular Biology. 8: 2435-41. PMID 2841581  1
1987 Page DC, Mosher R, Simpson EM, Fisher EM, Mardon G, Pollack J, McGillivray B, de la Chapelle A, Brown LG. The sex-determining region of the human Y chromosome encodes a finger protein. Cell. 51: 1091-104. PMID 3690661 DOI: 10.1016/0092-8674(87)90595-2  1
1985 Parker RC, Mardon G, Lebo RV, Varmus HE, Bishop JM. Isolation of duplicated human c-src genes located on chromosomes 1 and 20. Molecular and Cellular Biology. 5: 831-8. PMID 2581127  1
1983 Mardon G, Varmus HE. Frameshift and intragenic suppressor mutations in a Rous sarcoma provirus suggest src encodes two proteins. Cell. 32: 871-9. PMID 6299579 DOI: 10.1016/0092-8674(83)90072-7  1
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