| 1 | LAMP2, LGALS9
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| Lumenal Galectin-9-Lamp2 interaction regulates lysosome and autophagy to prevent pathogenesis in the intestine and pancreas.
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| Sudhakar JN, Lu HH, Chiang HY, Suen CS, Hwang MJ, Wu SY, Shen CN, Chang YM, Li FA, Liu FT, Shui JW.
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| Nat Commun. Aug 27;11(1):4286. doi: 10.1038/s41467-020-18102-7. 2020
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| 2 | LAMP2
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| The Lysosomal Membrane Protein Lamp2 Alleviates Lysosomal Cell Death by Promoting Autophagic Flux in Ischemic Cardiomyocytes
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| Cui L, Zhao LP, Ye JY, Yang L, Huang Y, Jiang XP, Zhang Q, Jia JZ, Zhang DX, Huang Y.
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| Front Cell Dev Biol. Feb 7;8:31. doi: 10.3389/fcell.2020.00031. 2020
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| 3 | LAMP2
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| Genetic LAMP2 deficiency accelerates the age-associated formation of basal laminar deposits in the retina
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| Notomi S, Ishihara K, Efstathiou NE, Lee JJ, Hisatomi T, Tachibana T, Konstantinou EK, Ueta T, Murakami Y, Maidana DE, Ikeda Y, Kume S, Terasaki H, Sonoda S, Blanz J, Young L, Sakamoto T, Sonoda KH, Saftig P, Ishibashi T, Miller JW, Kroemer G, Vavvas DG.
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| Proc Natl Acad Sci U S A. Nov 19;116(47):23724-23734. doi: 10.1073/pnas.1906643116. Epub 2019 Nov 7. 2019
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| 4 | LAMP2, SNAI1
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| Lamp2 inhibits epithelial-mesenchymal transition by suppressing Snail expression in HCC
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| Zheng H, Yang Y, Ye C, Li PP, Wang ZG, Xing H, Ren H, Zhou WP.
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| Oncotarget. Jul 13;9(54):30240-30252. doi: 10.18632/oncotarget.25367. 2018
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| 5 | GSD2B, LAMP2
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| LAMP2 exon-copy number variations in Danon disease heterozygote female probands: Infrequent or underdetected?
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| Majer F, Piherova L, Reboun M, Stara V, Pelak O, Norambuena P, Stranecky V, Krebsova A, Vlaskova H, Dvorakova L, Kmoch S, Kalina T, Kubanek M, Sikora J.
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| Am J Med Genet A. Nov;176(11):2430-2434. doi: 10.1002/ajmg.a.40430. Epub 2018 Sep 8. 2018
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| 6 | LAMP2
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| High expression of LAMP2 predicts poor prognosis in patients with esophageal squamous cell carcinoma
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| Li L, Wang W, Zhang R, Liu J, Yu J, Wu X, Xu Y, Ma M, Huang J.
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| Cancer Biomark. Jul 4;19(3):305-311. doi: 10.3233/CBM-160469. 2017
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| 7 | LAMP1, LAMP2
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| Lysosome-associated membrane proteins-1 and -2 (LAMP-1 and LAMP-2) assemble via distinct modes
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| Terasawa K, Tomabechi Y, Ikeda M, Ehara H, Kukimoto-Niino M, Wakiyama M, Podyma-Inoue KA, Rajapakshe AR, Watabe T, Shirouzu M, Hara-Yokoyama M.
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| Biochem Biophys Res Commun. Oct 21;479(3):489-495. doi: 10.1016/j.bbrc.2016.09.093. Epub 2016 Sep 20. 2016
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| 8 | LAMP2, MTOR, WDFY1
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| Angiogenic growth factor axis in autophagy regulation
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| Stanton MJ, Dutta S, Polavaram NS, Roy S, Muders MH, Datta K.
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| Autophagy. May;9(5):789-90. doi: 10.4161/auto.23783. Epub 2013 Feb 6. 2013
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| 9 | LAMP2
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| Profound left ventricular remodeling associated with LAMP2 cardiomyopathy.
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| Maron BJ, Roberts WC, Ho CY, Kitner C, Haas TS, Wright GB, Moazami N, Feldman DS.
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| Am J Cardiol. Oct 15;106(8):1194-6. doi: 10.1016/j.amjcard.2010.06.035. 2010
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| 10 | LAMP2, NKX2-5, PRKAG2
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| Molecular analysis of PRKAG2, LAMP2, and NKX2-5 genes in a cohort of 125 patients with accessory atrioventricular connection.
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| Esposito G, Grutter G, Drago F, Costa MW, De Santis A, Bosco G, Marino B, Bellacchio E, Lepri F, Harvey RP, Sarkozy A, Dallapiccola B.
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| Am J Med Genet A 149A(7):1574-7. No abstract available. PMID: 19533775 2009
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| 11 | LAMP1, LAMP2
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| Differential expression of LAMPs and ubiquitin in human thymus.
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| Sarafian VS, Marinova TT, Gulubova MV.
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| APMIS 117(4):248-52.
2009
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| 12 | LAMP2
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| Molecular mimicry in pauci-immune focal necrotizing glomerulonephritis.
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| Kain R, Exner M, Brandes R, Ziebermayr R, Cunningham D, Alderson CA, Davidovits A, Raab I, Jahn R, Ashour O, Spitzauer S, Sunder-Plassmann G, Fukuda M, Klemm P, Rees AJ, Kerjaschki D.
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| Nat Med 14(10):1088-96. Epub 2008 Oct 5.
2008
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| 13 | GSD2B, LAMP2
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| Danon disease: a novel Lamp-2 gene mutation in a family with four affected members.
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| Tuñón T, Guerrero D, Urchaga A, Nishino I, Ayuso T, Matsuda Y, Caballero MC, Berjón J, Imizcoz MA.
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| Neuromuscul Disord 18(2):167-74. Epub 2007 Dec 3.PMID: 18061453 2008
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| 14 | CTSE, SCARB1, SCARB2, LAMP1, LAMP2
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| Cathepsin E deficiency induces a novel form of lysosomal storage disorder showing the accumulation of lysosomal membrane sialoglycoproteins and the elevation of lysosomal pH in macrophages.
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| Yanagawa M, Tsukuba T, Nishioku T, Okamoto Y, Okamoto K, Takii R, Terada Y, Nakayama KI, Kadowaki T, Yamamoto K.
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| J Biol Chem 282(3):1851-62. Epub 2006 Nov 9. 2007
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| 15 | LAMP2, GSD2B
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| Danon disease presenting with dilated cardiomyopathy and a complex phenotype.
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| Taylor MR, Ku L, Slavov D, Cavanaugh J, Boucek M, Zhu X, Graw S, Carniel E, Barnes C, Quan D, Prall R, Lovell MA, Mierau G, Ruegg P, Mandava N, Bristow MR, Towbin JA, Mestroni L; Familial Cardiomyopathy Registry.
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| J Hum Genet 52(10):830-5. 2007
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| 16 | LAMP1, LAMP2
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| LAMP proteins are required for fusion of lysosomes with phagosomes.
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| Huynh KK, Eskelinen EL, Scott CC, Malevanets A, Saftig P, Grinstein S.
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| EMBO J 26(2):313-24.
2007
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| 17 | GSD2B, LAMP2
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| Morphological, clinical and genetic aspects in a family with a novel LAMP-2 gene mutation (Danon disease).
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| Lobrinus JA, Schorderet DF, Payot M, Jeanrenaud X, Bottani A, Superti-Furga A, Schlaepfer J, Fromer M, Jeannet PY.
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| Neuromuscul Disord 15(4):293-8. 2005
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| 18 | LAMP2, GSD2B
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| Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2gene.
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| Balmer C, Ballhausen D, Bosshard NU, Steinmann B, Boltshauser E, Bauersfeld U, Superti-Furga A.
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| Eur J Pediatr 164(8):509-14. Epub 2005 May 12. 2005
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| 19 | GSD2B, LAMP2
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| Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children.
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| Yang Z, McMahon CJ, Smith LR, Bersola J, Adesina AM, Breinholt JP, Kearney DL, Dreyer WJ, Denfield SW, Price JF, Grenier M, Kertesz NJ, Clunie SK, Fernbach SD, Southern JF, Berger S, Towbin JA, Bowles KR, Bowles NE.
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| Circulation 112(11):1612-7. Epub 2005 Sep 6. 2005
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| 20 | GSD2B,LAMP2
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| Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation.
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| Bertini E, Donati MA, Broda P, Cassandrini D, Petrini S, Dionisi-Vici C, Ballerini L, Boldrini R, D'Amico A, Pasquini E, Minetti C, Santorelli FM, Bruno C.
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| Neuropediatrics 36(5):309-13. 2005
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| 21 | LAMP2,MEAX
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| A new congenital form of X-linked autophagic vacuolar myopathy.
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| Yan C, Tanaka M, Sugie K, Nobutoki T, Woo M, Murase N, Higuchi Y, Noguchi S, Nonaka I, Hayashi YK, Nishino I.
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| Neurology 65(7):1132-4. 2005
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| 22 | LAMP1, LAMP2
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| Differential expression of lysosomal associated membrane protein (LAMP-1) during mammalian spermiogenesis.
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| Moreno RD.
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| Mol Reprod Dev 66(2):202-9.
2003
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| 23 | LAMP2, GSD2B
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| Germline mosaicism of a novel mutation in lysosome-associated membrane protein-2 deficiency (Danon disease).
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| Takahashi M, Yamamoto A, Takano K, Sudo A, Wada T, Goto Y, Nishino I, Saitoh S.
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| Ann Neurol 52(1):122-5. 2002
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| 24 | GSD2B, LAMP2
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| Danon's disease (X-linked vacuolar cardiomyopathy and myopathy): a case with a novel Lamp-2 gene mutation.
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| Lacoste-Collin L, Garcia V, Uro-Coste E, Arne-Bes MC, Durand D, Levade T, Delisle MB.
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| Neuromuscul Disord 12(9):882-5. 2002
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| 25 | LAMP2
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| Infantile autophagic vacuolar myopathy is distinct from Danon disease.
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| Yamamoto A, Morisawa Y, Verloes A, Murakami N, Hirano M, Nonaka I, Nishino I.
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| Neurology 57(5):903-5. 2001
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| 26 | LAMP2, MEAX
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| Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles.
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| Tsuruta Y, Furuta A, Furuta K, Yamada T, Kira J, Iwaki T.
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| Acta Neuropathol (Berl) 101(6):579-84. 2001
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| 27 | GSD2B, LAMP2
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| Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy.
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| Nishino I, Fu J, Tanji K, Yamada T, Shimojo S, Koori T, Mora M, Riggs JE, Oh SJ, Koga Y, Sue CM, Yamamoto A, Murakami N, Shanske S, Byrne E, Bonilla E, Nonaka I, DiMauro S, Hirano M.
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| Nature 406(6798):906-10. 2000
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| 28 | GSD2B, LAMP2
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| Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice.
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| Tanaka Y, Guhde G, Suter A, Eskelinen EL, Hartmann D, Lullmann-Rauch R, Janssen PM, Blanz J, von Figura K, Saftig P.
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| Nature 406(6798):902-6. 2000
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| 29 | APOA1, LAMP2, MEAX, NNHA
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| The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide.
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| Obici L, Bellotti V, Mangione P, Stoppini M, Arbustini E, Verga L, Zorzoli I, Anesi E, Zanotti G, Campana C, Viganò M, Merlini G.
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| Am J Pathol 155(3):695-702. 1999
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| 30 | LAMP1, LAMP2
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| The family of LAMP-2 proteins arises by alternative splicing from a single gene : characterization of the avian LAMP-2 gene and identification of mammalian homologs of LAMP-2b and LAMP-2c.
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| Gough NR, et al.
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| DNA Cell Biol 14 : 863-867. 1995
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| 31 | LAMP1, LAMP2
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| Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease.
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| Schleutker J, et al.
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| Hum Genet 88 : 95-97. 1991
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| 32 | LAMP2
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| The nucleotide sequence of a CpG island demonstrates the presence of the first exon of the gene encoding the human lysosomal membrane protein lamp2 and assigns the gene to Xq24.
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| Manoni M, et al.
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| Genomics 9 : 551-554. 1991
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| 33 | LAMP1, LAMP1L1, LAMP2
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| Two human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2, are encoded by genes localized to chromosome 13q34 and chromosome Xq24-25, respectively.
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| Mattei MG, et al.
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| J Biol Chem 265 : 7548-7551. 1990
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| 34 | LAMP2, DXS477
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| Probes for CpG islands on the distal long arm of the human X chromosome are clustered in Xq24 and Xq28.
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| Maestrini E, et al.
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| Genomics 8 : 664-670. 1990
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| 35 | LAMP1, LAMP2
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| Cloning of cDNAs encoding human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2. Comparison of their deduced amino acid sequences.
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| Fukuda M, et al.
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| J Biol Chem 263 : 18920-18928. 1988
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