| Year |
Citation |
Score |
| 2018 |
Kumari SS, Varadaraj M, Menon AG, Varadaraj K. Aquaporin 5 promotes corneal wound healing. Experimental Eye Research. 172: 152-158. PMID 29660329 DOI: 10.1016/J.Exer.2018.04.005 |
0.303 |
|
| 2015 |
Sindhu Kumari S, Gupta N, Shiels A, FitzGerald PG, Menon AG, Mathias RT, Varadaraj K. Role of Aquaporin 0 in lens biomechanics. Biochemical and Biophysical Research Communications. 462: 339-45. PMID 25960294 DOI: 10.1016/J.Bbrc.2015.04.138 |
0.321 |
|
| 2013 |
Aggarwal NR, Chau E, Garibaldi BT, Mock JR, Sussan T, Rao K, Rao K, Menon AG, D'Alessio FR, Damarla M, Biswal S, King LS, Sidhaye VK. Aquaporin 5 regulates cigarette smoke induced emphysema by modulating barrier and immune properties of the epithelium. Tissue Barriers. 1: e25248. PMID 24665410 DOI: 10.4161/Tisb.25248 |
0.302 |
|
| 2013 |
Kawedia JD, Yang F, Sartor MA, Gozal D, Czyzyk-Krzeska M, Menon AG. Hypoxia and hypoxia mimetics decrease aquaporin 5 (AQP5) expression through both hypoxia inducible factor-1α and proteasome-mediated pathways. Plos One. 8: e57541. PMID 23469202 DOI: 10.1371/Journal.Pone.0057541 |
0.366 |
|
| 2012 |
Menon AG, Klanke CA, Su YR. Identification of disease genes by positional cloning. Trends in Cardiovascular Medicine. 4: 97-102. PMID 21244887 DOI: 10.1016/1050-1738(94)90060-4 |
0.32 |
|
| 2010 |
Kikuchi K, Kawedia J, Menon AG, Hand AR. The structure of tight junctions in mouse submandibular gland. Anatomical Record (Hoboken, N.J. : 2007). 293: 141-9. PMID 19899114 DOI: 10.1002/Ar.21029 |
0.302 |
|
| 2007 |
Kawedia JD, Nieman ML, Boivin GP, Melvin JE, Kikuchi K, Hand AR, Lorenz JN, Menon AG. Interaction between transcellular and paracellular water transport pathways through Aquaporin 5 and the tight junction complex. Proceedings of the National Academy of Sciences of the United States of America. 104: 3621-6. PMID 17360692 DOI: 10.1073/Pnas.0608384104 |
0.31 |
|
| 2006 |
Ingraham SE, Lynch RA, Surti U, Rutter JL, Buckler AJ, Khan SA, Menon AG, Lepont P. Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma. Mutation Research. 602: 43-53. PMID 17045619 DOI: 10.1016/J.Mrfmmm.2006.07.007 |
0.73 |
|
| 2004 |
Gabazza EC, Kasper M, Ohta K, Keane M, D'Alessandro-Gabazza C, Fujimoto H, Nishii Y, Nakahara H, Takagi T, Menon AG, Adachi Y, Suzuki K, Taguchi O. Decreased expression of aquaporin-5 in bleomycin-induced lung fibrosis in the mouse. Pathology International. 54: 774-80. PMID 15482567 DOI: 10.1111/J.1440-1827.2004.01754.X |
0.344 |
|
| 2003 |
Merves M, Krane CM, Dou H, Greinwald JH, Menon AG, Choo D. Expression of aquaporin 1 and 5 in the developing mouse inner ear and audiovestibular assessment of an Aqp5 null mutant. Journal of the Association For Research in Otolaryngology : Jaro. 4: 264-75. PMID 12943377 DOI: 10.1007/S10162-002-3033-7 |
0.342 |
|
| 2003 |
Yang F, Kawedia JD, Menon AG. Cyclic AMP regulates aquaporin 5 expression at both transcriptional and post-transcriptional levels through a protein kinase A pathway. The Journal of Biological Chemistry. 278: 32173-80. PMID 12783871 DOI: 10.1074/Jbc.M305149200 |
0.366 |
|
| 2002 |
Nejsum LN, Kwon TH, Jensen UB, Fumagalli O, Frøkiaer J, Krane CM, Menon AG, King LS, Agre PC, Nielsen S. Functional requirement of aquaporin-5 in plasma membranes of sweat glands. Proceedings of the National Academy of Sciences of the United States of America. 99: 511-6. PMID 11773623 DOI: 10.1073/Pnas.012588099 |
0.337 |
|
| 2001 |
Krane CM, Fortner CN, Hand AR, McGraw DW, Lorenz JN, Wert SE, Towne JE, Paul RJ, Whitsett JA, Menon AG. Aquaporin 5-deficient mouse lungs are hyperresponsive to cholinergic stimulation. Proceedings of the National Academy of Sciences of the United States of America. 98: 14114-9. PMID 11707570 DOI: 10.1073/Pnas.231273398 |
0.682 |
|
| 2001 |
Krane CM, Melvin JE, Nguyen HV, Richardson L, Towne JE, Doetschman T, Menon AG. Salivary acinar cells from aquaporin 5-deficient mice have decreased membrane water permeability and altered cell volume regulation. The Journal of Biological Chemistry. 276: 23413-20. PMID 11290736 DOI: 10.1074/Jbc.M008760200 |
0.644 |
|
| 2001 |
Towne JE, Krane CM, Bachurski CJ, Menon AG. Tumor necrosis factor-alpha inhibits aquaporin 5 expression in mouse lung epithelial cells. The Journal of Biological Chemistry. 276: 18657-64. PMID 11279049 DOI: 10.1074/Jbc.M100322200 |
0.651 |
|
| 2000 |
Dalton TP, Miller ML, Wu X, Menon A, Cianciolo E, McKinnon RA, Smith PW, Robinson LJ, Nebert DW. Refining the mouse chromosomal location of Cdm, the major gene associated with susceptibility to cadmium-induced testicular necrosis. Pharmacogenetics. 10: 141-51. PMID 10762002 DOI: 10.1097/00008571-200003000-00006 |
0.361 |
|
| 2000 |
Towne JE, Harrod KS, Krane CM, Menon AG. Decreased expression of aquaporin (AQP)1 and AQP5 in mouse lung after acute viral infection. American Journal of Respiratory Cell and Molecular Biology. 22: 34-44. PMID 10615063 DOI: 10.1165/Ajrcmb.22.1.3818 |
0.66 |
|
| 1999 |
Ingraham SE, Lynch RA, Kathiresan S, Buckler AJ, Menon AG. hREC2, a RAD51-like gene, is disrupted by t(12;14)(q15;q24.1) in a uterine leiomyoma Cancer Genetics and Cytogenetics. 115: 56-61. PMID 10565301 DOI: 10.1016/S0165-4608(99)00070-9 |
0.723 |
|
| 1999 |
Deimling Av, Larson J, Wellenreuther R, Stangl AP, Velthoven Vv, Warnick R, Tew J, Balko G, Menon AG. Clonal origin of recurrent meningiomas. Brain Pathology. 9: 645-650. PMID 10517503 DOI: 10.1111/J.1750-3639.1999.Tb00546.X |
0.302 |
|
| 1999 |
Krane CM, Towne JE, Menon AG. Cloning and characterization of murine Aqp5: evidence for a conserved aquaporin gene cluster. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 498-505. PMID 10337625 DOI: 10.1007/S003359901030 |
0.683 |
|
| 1999 |
Baird NR, Orlowski J, Szabó EZ, Zaun HC, Schultheis PJ, Menon AG, Shull GE. Molecular cloning, genomic organization, and functional expression of Na+/H+ exchanger isoform 5 (NHE5) from human brain. The Journal of Biological Chemistry. 274: 4377-82. PMID 9933641 DOI: 10.1074/Jbc.274.7.4377 |
0.348 |
|
| 1998 |
Einum DD, Zhang J, Arneson PJ, Menon AG, Ptacek LJ. Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological disease. Neurogenetics. 1: 289-92. PMID 10732805 DOI: 10.1007/S100480050043 |
0.313 |
|
| 1998 |
Lynch RA, Piper M, Bankier A, Bhugra B, Surti U, Liu J, Buckler A, Dear PH, Menon AG. Genomic and functional map of the chromosome 14 t(12; 14) breakpoint cluster region in uterine leiomyoma Genomics. 52: 17-26. PMID 9740667 DOI: 10.1006/Geno.1998.5406 |
0.398 |
|
| 1998 |
Rutkowski MP, Klanke CA, Su YR, Reif M, Menon AG. Genetic markers at the leptin (OB) locus are not significantly linked to hypertension in African Americans. Hypertension (Dallas, Tex. : 1979). 31: 1230-4. PMID 9622134 DOI: 10.1161/01.Hyp.31.6.1230 |
0.302 |
|
| 1998 |
Bhugra B, Smolarek TA, Lynch RA, Meloni AM, Sandberg AA, Deaven L, Menon AG. Cloning of a breakpoint cluster region on chromosome 14 in uterine leiomyoma. Cancer Letters. 126: 119-26. PMID 9585056 DOI: 10.1016/S0304-3835(97)00478-3 |
0.392 |
|
| 1998 |
Smolarek TA, Wessner LL, McCormack FX, Mylet JC, Menon AG, Henske EP. Evidence that lymphangiomyomatosis is caused by TSC2 mutations: chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosis. American Journal of Human Genetics. 62: 810-5. PMID 9529362 DOI: 10.1086/301804 |
0.366 |
|
| 1998 |
Cruz M, Elenich LA, Smolarek TA, Menon AG, Monaco JJ. DNA sequence, chromosomal localization, and tissue expression of the mouse proteasome subunit lmp10 (Psmb10) gene. Genomics. 45: 618-22. PMID 9367687 DOI: 10.1006/Geno.1997.4977 |
0.434 |
|
| 1997 |
Micka J, Milatovich A, Menon A, Grabowski GA, Puga A, Nebert DW. Human Ah receptor (AHR) gene: Localization to 7p15 and suggestive correlation of polymorphism with CYP1A1 inducibility Pharmacogenetics. 7: 95-101. PMID 9170146 DOI: 10.1097/00008571-199704000-00002 |
0.368 |
|
| 1997 |
Stangl AP, Wellenreuther R, Lenartz D, Kraus JA, Menon AG, Schramm J, Wiestler OD, Von Deimling A. Clonality of multiple meningiomas Journal of Neurosurgery. 86: 853-858. PMID 9126902 DOI: 10.1097/00041327-199712000-00036 |
0.335 |
|
| 1997 |
Menon AG, Rutter JL, von Sattel JP, Synder H, Murdoch C, Blumenfeld A, Martuza RL, von Deimling A, Gusella JF, Houseal TW. Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putative 'tumor progression' locus. Oncogene. 14: 611-6. PMID 9053860 DOI: 10.1038/Sj.Onc.1200853 |
0.364 |
|
| 1997 |
Simon M, Kokkino AJ, Warnick RE, Tew JM, von Deimling A, Menon AG. Role of genomic instability in meningioma progression. Genes, Chromosomes & Cancer. 16: 265-9. PMID 8875241 DOI: 10.1002/(Sici)1098-2264(199608)16:4<265::Aid-Gcc7>3.0.Co;2-W |
0.389 |
|
| 1996 |
Shinoura N, Chen L, Wani MA, Kim YG, Larson JJ, Warnick RE, Simon M, Menon AG, Bi WL, Stambrook PJ. Protein and messenger RNA expression of connexin43 in astrocytomas: implications in brain tumor gene therapy. Journal of Neurosurgery. 84: 839-45; discussion 8. PMID 8622159 DOI: 10.3171/Jns.1996.84.5.0839 |
0.354 |
|
| 1995 |
Burk SE, Menon AG, Shull GE. Analysis of the 5' end of the rat plasma membrane Ca(2+)-ATPase isoform 3 gene and identification of extensive trinucleotide repeat sequences in the 5' untranslated region. Biochimica Et Biophysica Acta. 1240: 119-24. PMID 8541282 DOI: 10.1016/0005-2736(95)00217-0 |
0.302 |
|
| 1995 |
Linn SC, Askew GR, Menon AG, Shull GE. Conservation of an AE3 Cl-/HCO3- exchanger cardiac-specific exon and promoter region and AE3 mRNA expression patterns in murine and human hearts. Circulation Research. 76: 584-91. PMID 7895333 DOI: 10.1161/01.Res.76.4.584 |
0.316 |
|
| 1995 |
Shinoura N, Shamraj OI, Hugenholz H, Zhu JG, McBlack P, Warnick R, Tew JJ, Wani MA, Menon AG. Identification and partial sequence of a cDNA that is differentially expressed in human brain tumors. Cancer Letters. 89: 215-21. PMID 7889532 DOI: 10.1016/0304-3835(95)03690-X |
0.344 |
|
| 1995 |
Klanke CA, Su YR, Callen DF, Wang Z, Meneton P, Baird N, Kandasamy RA, Orlowski J, Otterud BE, Leppert M, Shull GE, Menon AG. Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1 Genomics. 25: 615-622. PMID 7759094 DOI: 10.1016/0888-7543(95)80002-4 |
0.418 |
|
| 1995 |
Larson JJ, Tew JM, Simon M, Menon AG. Evidence for clonal spread in the development of multiple meningiomas. Journal of Neurosurgery. 83: 705-9. PMID 7674021 DOI: 10.3171/Jns.1995.83.4.0705 |
0.346 |
|
| 1995 |
Deimling Av, Krone W, Menon AG. Neurofibromatosis type 1: pathology, clinical features and molecular genetics. Brain Pathology. 5: 153-162. PMID 7670656 DOI: 10.1111/J.1750-3639.1995.Tb00589.X |
0.368 |
|
| 1995 |
Doney MK, Gerken SC, Lynch R, Bhugra B, Hug K, White R, Weissenbach J, Menon AG. Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540. Cancer Letters. 96: 245-52. PMID 7585464 DOI: 10.1016/0304-3835(95)03938-S |
0.399 |
|
| 1994 |
Bianchi AB, Hara T, Ramesh V, Gao J, Klein-Szanto AJ, Morin F, Menon AG, Trofatter JA, Gusella JF, Seizinger BR. Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types. Nature Genetics. 6: 185-92. PMID 8162073 DOI: 10.1038/Ng0294-185 |
0.34 |
|
| 1994 |
Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG. Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36. Genomics. 22: 605-9. PMID 8001971 DOI: 10.1006/Geno.1994.1433 |
0.414 |
|
| 1994 |
Hug K, Doney MK, Tyler MJ, Grundy DA, Soukup S, Houseal TW, Menon AG. Physical mapping of the uterine leiomyoma t(12;14)(q13-15;q24.1) breakpoint on chromosome 14 between SPTB and D14S77. Genes, Chromosomes & Cancer. 11: 263-6. PMID 7533530 DOI: 10.1002/Gcc.2870110409 |
0.421 |
|
| 1994 |
Shinoura N, Heffelfinger SC, Miller M, Shamraj OI, Miura NC, Larson JJ, DeTribolet N, Warnick RE, Tew JJ, Menon AG. RNA expression of complement regulatory proteins in human brain tumors. Cancer Letters. 86: 143-149. PMID 7526972 DOI: 10.1016/0304-3835(94)90072-8 |
0.341 |
|
| 1994 |
Menon AG, Gusella JF, Seizinger BR. Progress toward the isolation and characterization of the genes causing neurofibromatosis. Brain Pathology (Zurich, Switzerland). 1: 33-40. PMID 1669691 DOI: 10.1111/J.1750-3639.1990.Tb00636.X |
0.398 |
|
| 1994 |
Riegman PH, Lekanne Deprez RH, Groen N, Kortenhorst U, Hagemeijer A, van Drunen E, Bootsma D, Menon A, Kley N, Seizinger BR, de Jong P, Zwarthoff EC. Cloning of a putative meningioma tumor suppressor gene Cancer Genetics and Cytogenetics. 77: 174. DOI: 10.1016/0165-4608(94)90331-X |
0.333 |
|
| 1993 |
The I, Murthy AE, Hannigan GE, Jacoby LB, Menon AG, Gusella JF, Bernards A. Neurofibromatosis type 1 gene mutations in neuroblastoma. Nature Genetics. 3: 62-6. PMID 8490657 DOI: 10.1038/Ng0193-62 |
0.331 |
|
| 1993 |
MacCollin M, Romano D, Budarf M, Denny C, Trofatter J, Menon A, Rouleau G, Fontaine B, Emanuel B, Gusella J. A set of STS assays targeting the chromosome 22 physical framework markers. Genomics. 15: 680-3. PMID 8468063 DOI: 10.1006/Geno.1993.1125 |
0.354 |
|
| 1993 |
Trofatter JA, MacCollin MM, Rutter JL, Murrell JR, Duyao MP, Parry DM, Eldridge R, Kley N, Menon AG, Pulaski K. A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell. 72: 791-800. PMID 8453669 DOI: 10.1016/0092-8674(93)90406-G |
0.39 |
|
| 1993 |
von Deimling A, Louis DN, Menon AG, von Ammon K, Petersen I, Ellison D, Wiestler OD, Seizinger BR. Deletions on the long arm of chromosome 17 in pilocytic astrocytoma. Acta Neuropathologica. 86: 81-5. PMID 8103960 DOI: 10.1007/Bf00454903 |
0.431 |
|
| 1992 |
Bernards A, Haase VH, Murthy AE, Menon A, Hannigan GE, Gusella JF. Complete human NF1 cDNA sequence: two alternatively spliced mRNAs and absence of expression in a neuroblastoma line. Dna and Cell Biology. 11: 727-34. PMID 1457041 DOI: 10.1089/Dna.1992.11.727 |
0.391 |
|
| 1991 |
Fontaine B, Rouleau GA, Seizinger BR, Menon AG, Jewell AF, Martuza RL, Gusella JF. Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma). Annals of the New York Academy of Sciences. 615: 338-43. PMID 2039155 DOI: 10.1111/J.1749-6632.1991.Tb37776.X |
0.347 |
|
| 1991 |
Chung R, Whaley J, Kley N, Anderson K, Louis D, Menon A, Hettlich C, Freiman R, Hedley-Whyte ET, Martuza R. TP53 gene mutations and 17p deletions in human astrocytomas. Genes, Chromosomes & Cancer. 3: 323-31. PMID 1686725 DOI: 10.1002/Gcc.2870030502 |
0.381 |
|
| 1991 |
Fontaine B, Sanson M, Delattre O, Menon AG, Rouleau GA, Seizinger BR, Jewell AF, Hanson MP, Aurias A, Martuza RL. Parental origin of chromosome 22 loss in sporadic and NF2 neuromas. Genomics. 10: 280-3. PMID 1675196 DOI: 10.1016/0888-7543(91)90513-E |
0.353 |
|
| 1990 |
Menon AG, Anderson KM, Riccardi VM, Chung RY, Whaley JM, Yandell DW, Farmer GE, Freiman RN, L-Ee JK, Li FP, Barker DF, Ledbetter DH, Kleider A, Martuza RL, Gusella JF, et al. Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis Proceedings of the National Academy of Sciences of the United States of America. 87: 5435-5439. PMID 2142531 DOI: 10.1073/Pnas.87.14.5435 |
0.415 |
|
| 1990 |
Haines JL, Ozelius LJ, McFarlane H, Menon A, Tzall S, Martiniuk F, Hirschhorn R, Gusella JF. A genetic linkage map of chromosome 17. Genomics. 8: 1-6. PMID 2081586 DOI: 10.1016/0888-7543(90)90218-J |
0.317 |
|
| 1989 |
Fountain JW, Wallace MR, Bruce MA, Seizinger BR, Menon AG, Gusella JF, Michels VV, Schmidt MA, Dewald GW, Collins FS. Physical mapping of a translocation breakpoint in neurofibromatosis Science. 244: 1085-1087. PMID 2543076 DOI: 10.1126/Science.2543076 |
0.391 |
|
| 1989 |
Menon AG, Ledbetter DH, Rich DC, Seizinger BR, Rouleau GA, Michels VF, Schmidt MA, Dewald G, DallaTorre CM, Haines JL. Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17. Genomics. 5: 245-9. PMID 2507442 DOI: 10.1016/0888-7543(89)90053-0 |
0.414 |
|
| 1987 |
Seizinger BR, Rouleau GA, Lane AH, Farmer G, Ozelius LJ, Haines JL, Parry DM, Korf BR, Pericak-Vance MA, Faryniarz AG, Hobbs WJ, Iannazzi JA, Roy JC, Menon A, Bader JL, et al. Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17 Genomics. 1: 346-348. PMID 2896628 DOI: 10.1016/0888-7543(87)90035-8 |
0.419 |
|
| 1986 |
Menon AG, Lingrel JB. Structural and functional analysis of the goat epsilon-globin genes. Gene. 42: 141-50. PMID 3015728 DOI: 10.1016/0378-1119(86)90290-8 |
0.323 |
|
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