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• Malfait, F., Francomano, C., Byers, P., Belmont, J., Berglund, B., Black, J., Bloom, L., Bowen, J.M., Brady, A.F., Burrows, N.P. et al. (2017) The 2017 international classification of the Ehlers-Danlos syndromes. Am. J. Med. Genet. C Semin. Med. Genet., 175, 8-26.
• Alazami, A.M., Al-Qattan, S.M., Faqeih, E., Alhashem, A., Alshammari, M., Alzahrani, F., Al-Dosari, M.S., Patel, N., Alsagheir, A., Binabbas, B. et al. (2016) Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue. Hum. Genet., 135, 525-540.
• Blackburn, P.R., Xu, Z., Tumelty, K.E., Zhao, R.W., Monis, W.J., Harris, K.G., Gass, J.M., Cousin, M.A., Boczek, N.J., Mitkov, M.V. et al. (2018) Bi-Allelic alterations in AEBP1 lead to defective collagen assembly and connective tissue structure resulting in a variant of Ehlers-Danlos syndrome. Am. J. Hum. Genet., 102, 696-705.
• Layne, M.D., Yet, S.F., Maemura, K., Hsieh, C.M., Bernfield, M., Perrella, M.A. and Lee, M.E. (2001) Impaired abdominal wall development and deficient wound healing in mice lacking aortic carboxypeptidase-like protein. Mol. Cell. Biol., 21, 5256-5261.
• Ith, B., Wei, J., Yet, S.F., Perrella, M.A. and Layne, M.D. (2005) Aortic carboxypeptidase-like protein is expressed in collagen-rich tissues during mouse embryonic development. Gene Expr. Patterns, 5, 533-537.
• Voermans, N.C., van Alfen, N., Pillen, S., Lammens, M., Schalkwijk, J., Zwarts, M.J., van Rooij, I.A., Hamel, B.C.J. and van Engelen, B.G. (2009) Neuromuscular involvement in various types of Ehlers-Danlos syndrome. Ann. Neurol., 65, 687-697.
• Lyons, P.J., Mattatall, N.R. and Ro, H.S. (2006) Modeling and functional analysis of AEBP1, a transcriptional repressor. Proteins, 63, 1069-1083.
• Schissel, S.L., Dunsmore, S.E., Liu, X., Shine, R.W., Perrella, M.A. and Layne, M.D. (2009) Aortic carboxypeptidase-like protein is expressed in fibrotic human lung and its absence protects against bleomycin-induced lung fibrosis. Am. J. Pathol., 174, 818-828.
• Tumelty, K.E., Smith, B.D., Nugent, M.A. and Layne, M.D. (2014) Aortic carboxypeptidase-like protein (ACLP) enhances lung myofibroblast differentiation through transforming growth factor β receptor-dependent and-independent pathways. J. Biol. Chem., 289, 2526-2536.
• Jager, M., Lee, M.J., Li, C., Farmer, S.R., Fried, S.K. and Layne, M.D. (2018) Aortic carboxypeptidase-like protein enhances adipose tissue stromal progenitor differentiation into myofibroblasts and is upregulated in fibrotic white adipose tissue. PLoS One, 13, e0197777.
• Teratani, T., Tomita, K., Suzuki, T., Furuhashi, H., Irie, R., Nishikawa, M., Yamamoto, J., Hibi, T., Miura, S., Minamino, T. et al. (2018) Aortic carboxypeptidase-like protein, a WNT ligand, exacerbates nonalcoholic steatohepatitis. J. Clin. Invest., 128, 1581-1596.
• Zhong, Z., Ethen, N.J. andWilliams, B.O. (2014)WNTsignaling in bone development and homeostasis.Wiley Interdiscip. Rev. Dev. Biol., 3, 489-500.
• Iguez-Ariza, N.M. and Clarke, B.L. (2015) Bone biology, signaling pathways, and therapeutic targets for osteoporosis. Maturitas, 82, 245-255.
• Symoens, S., Syx, D., Malfait, F., Callewaert, B., De Backer, J., Vanakker, O., Coucke, P. and De Paepe, A. (2012) Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria. Hum. Mutat., 33, 1485-1493.
• den Dunnen, J.T., Dalgleish, R., Maglott, D.R., Hart, R.K., Greenblatt, M.S., McGowan-Jordan, J., Roux, A.F., Smith, T., Antonarakis, S.E. and Taschner, P.E.M. (2016) HGVS recommendations for the description of sequence variants: 2016 update. Hum. Mutat., 37, 564-569.
• Richards, S., Aziz, N., Bale, S., Bick, D., Das, S., Gastier-Foster, J., Grody, W.W., Hegde, M., Lyon, E., Spector, E. et al. (2015) Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet. Med., 17, 405-424.
• Menten, B., Pattyn, F., De Preter, K., Robbrecht, P., Michels, E., Buysse, K., Mortier, G., De Paepe, A., van Vooren, S., Vermeesch, J. et al . (2005) arrayCGHbase: An analysis platform for comparative genomic hybridization microarrays. BMC Bioinformatics, 6, 124.
• Steinmann, B., Eyre, D.R. and Shao, P. (1995) Urinary pyridinoline cross-links in Ehlers-Danlos syndrome type VI. Am. J. Hum. Genet., 57, 1505-1508.
• Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B. et al. (2012) Fiji: An open-source platform for biological-image analysis. Nat. Methods, 9, 676-682.