Hereditary mucoepithelial dysplasia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hereditary mucoepithelial dysplasia" in English language version.

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  • Bredrup, C.; Knappskog, P. M.; Majewski, J.; Rødahl, E.; Boman, H. (February 2005). "Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene". Invest Ophthalmol Vis Sci. 46 (2): 420–426. doi:10.1167/iovs.04-0804. PMID 15671264.
  • Putran J, S. C.; Sowden, C. (October 2007). "Abnormal cervical smear in hereditary mucoepithelial dysplasia: a case report". Journal of Lower Genital Tract Disease. 11 (4): 274–275. doi:10.1097/LGT.0b013e31803c4de0. ISSN 1089-2591. PMID 17917573.
  • Scheman, A.; Ray, D.; Witkop Jr, C.; Dahl, M. (Aug 1989). "Hereditary mucoepithelial dysplasia. Case report and review of the literature". Journal of the American Academy of Dermatology. 21 (2 Pt 2): 351–357. doi:10.1016/S0190-9622(89)80033-7. ISSN 0190-9622. PMID 2666466.
  • Rogers, M.; Kourt, G.; Cameron, A. (Jun 1994). "Hereditary mucoepithelial dysplasia". Pediatric Dermatology. 11 (2): 133–138. doi:10.1111/j.1525-1470.1994.tb00567.x. ISSN 0736-8046. PMID 8041653. S2CID 39481017.
  • Huber, O. (Sep 2003). "Structure and function of desmosomal proteins and their role in development and disease". Cellular and Molecular Life Sciences. 60 (9): 1872–1890. doi:10.1007/s00018-003-3050-7. ISSN 1420-682X. PMC 11138567. PMID 14523549. S2CID 11557417.
  • Lampe, P. D.; Lau, A. F. (Jul 2004). "The effects of connexin phosphorylation on gap junctional communication". The International Journal of Biochemistry & Cell Biology (Free full text). 36 (7): 1171–1186. doi:10.1016/S1357-2725(03)00264-4. ISSN 1357-2725. PMC 2878204. PMID 15109565.
  • Lampe, P.; Lau, A. F. (Dec 2000). "Regulation of gap junctions by phosphorylation of connexins". Archives of Biochemistry and Biophysics. 384 (2): 205–215. doi:10.1006/abbi.2000.2131. ISSN 0003-9861. PMID 11368307.
  • Freundlich, E.; Amit, S.; Montag, Y.; Suprun, H.; Nevo, S. (February 1972). "Familial Occurrence of Letterer-Siwe Disease". Archives of Disease in Childhood (Free full text). 47 (251): 122–125. doi:10.1136/adc.47.251.122. PMC 1647995. PMID 5018627.

nih.gov

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  • Bredrup, C.; Knappskog, P. M.; Majewski, J.; Rødahl, E.; Boman, H. (February 2005). "Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene". Invest Ophthalmol Vis Sci. 46 (2): 420–426. doi:10.1167/iovs.04-0804. PMID 15671264.
  • Putran J, S. C.; Sowden, C. (October 2007). "Abnormal cervical smear in hereditary mucoepithelial dysplasia: a case report". Journal of Lower Genital Tract Disease. 11 (4): 274–275. doi:10.1097/LGT.0b013e31803c4de0. ISSN 1089-2591. PMID 17917573.
  • Scheman, A.; Ray, D.; Witkop Jr, C.; Dahl, M. (Aug 1989). "Hereditary mucoepithelial dysplasia. Case report and review of the literature". Journal of the American Academy of Dermatology. 21 (2 Pt 2): 351–357. doi:10.1016/S0190-9622(89)80033-7. ISSN 0190-9622. PMID 2666466.
  • Witkop Jr, C. J.; White, J. G.; King, R. A.; Dahl, M. V.; Young, W. G.; Sauk Jr, J. J. (Jul 1979). "Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation". American Journal of Human Genetics. 31 (4): 414–427. ISSN 0002-9297. PMC 1685894. PMID 484550.
  • Rogers, M.; Kourt, G.; Cameron, A. (Jun 1994). "Hereditary mucoepithelial dysplasia". Pediatric Dermatology. 11 (2): 133–138. doi:10.1111/j.1525-1470.1994.tb00567.x. ISSN 0736-8046. PMID 8041653. S2CID 39481017.
  • Witkop Jr, C. J.; White, J. G.; Waring, G. O. (1982). "Hereditary mucoepithelial dysplasia, a disease of gap junction and desmosome formation". Birth Defects Original Article Series. 18 (6): 493–511. ISSN 0547-6844. PMID 7171771.
  • Huber, O. (Sep 2003). "Structure and function of desmosomal proteins and their role in development and disease". Cellular and Molecular Life Sciences. 60 (9): 1872–1890. doi:10.1007/s00018-003-3050-7. ISSN 1420-682X. PMC 11138567. PMID 14523549. S2CID 11557417.
  • Lampe, P. D.; Lau, A. F. (Jul 2004). "The effects of connexin phosphorylation on gap junctional communication". The International Journal of Biochemistry & Cell Biology (Free full text). 36 (7): 1171–1186. doi:10.1016/S1357-2725(03)00264-4. ISSN 1357-2725. PMC 2878204. PMID 15109565.
  • Lampe, P.; Lau, A. F. (Dec 2000). "Regulation of gap junctions by phosphorylation of connexins". Archives of Biochemistry and Biophysics. 384 (2): 205–215. doi:10.1006/abbi.2000.2131. ISSN 0003-9861. PMID 11368307.
  • Freundlich, E.; Amit, S.; Montag, Y.; Suprun, H.; Nevo, S. (February 1972). "Familial Occurrence of Letterer-Siwe Disease". Archives of Disease in Childhood (Free full text). 47 (251): 122–125. doi:10.1136/adc.47.251.122. PMC 1647995. PMID 5018627.

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