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Disease relevance of Telangiectasis


Psychiatry related information on Telangiectasis


High impact information on Telangiectasis


Chemical compound and disease context of Telangiectasis


Biological context of Telangiectasis


Anatomical context of Telangiectasis


Gene context of Telangiectasis


Analytical, diagnostic and therapeutic context of Telangiectasis


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  2. Liver disease in patients with hereditary hemorrhagic telangiectasia. Garcia-Tsao, G., Korzenik, J.R., Young, L., Henderson, K.J., Jain, D., Byrd, B., Pollak, J.S., White, R.I. N. Engl. J. Med. (2000) [Pubmed]
  3. Antifibrillarin autoantibodies present in systemic sclerosis and other connective tissue diseases interact with similar epitopes. Kasturi, K.N., Hatakeyama, A., Spiera, H., Bona, C.A. J. Exp. Med. (1995) [Pubmed]
  4. Aerosolized prostacyclin and iloprost in severe pulmonary hypertension. Olschewski, H., Walmrath, D., Schermuly, R., Ghofrani, A., Grimminger, F., Seeger, W. Ann. Intern. Med. (1996) [Pubmed]
  5. Atm and Bax cooperate in ionizing radiation-induced apoptosis in the central nervous system. Chong, M.J., Murray, M.R., Gosink, E.C., Russell, H.R., Srinivasan, A., Kapsetaki, M., Korsmeyer, S.J., McKinnon, P.J. Proc. Natl. Acad. Sci. U.S.A. (2000) [Pubmed]
  6. Cytogenetic study in a mentally retarded child with Bloom syndrome and acute lymphoblastic leukemia. Werner-Favre, C., Wyss, M., Cabrol, C., Félix, F., Guenin, R., Laufer, D., Engel, E. Am. J. Med. Genet. (1984) [Pubmed]
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  8. Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice. Bonyadi, M., Rusholme, S.A., Cousins, F.M., Su, H.C., Biron, C.A., Farrall, M., Akhurst, R.J. Nat. Genet. (1997) [Pubmed]
  9. Heterozygous ATM mutations do not contribute to early onset of breast cancer. FitzGerald, M.G., Bean, J.M., Hegde, S.R., Unsal, H., MacDonald, D.J., Harkin, D.P., Finkelstein, D.M., Isselbacher, K.J., Haber, D.A. Nat. Genet. (1997) [Pubmed]
  10. Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. Johnson, D.W., Berg, J.N., Baldwin, M.A., Gallione, C.J., Marondel, I., Yoon, S.J., Stenzel, T.T., Speer, M., Pericak-Vance, M.A., Diamond, A., Guttmacher, A.E., Jackson, C.E., Attisano, L., Kucherlapati, R., Porteous, M.E., Marchuk, D.A. Nat. Genet. (1996) [Pubmed]
  11. Atm-deficient mice: a paradigm of ataxia telangiectasia. Barlow, C., Hirotsune, S., Paylor, R., Liyanage, M., Eckhaus, M., Collins, F., Shiloh, Y., Crawley, J.N., Ried, T., Tagle, D., Wynshaw-Boris, A. Cell (1996) [Pubmed]
  12. Defective DNA repair and increased lethality in ataxia telangiectasia cells exposed to 4-nitroquinoline-1-oxide. Smith, P.J., Paterson, M.C. Nature (1980) [Pubmed]
  13. Nifedipine and telangiectasias. Tsele, E., Chu, A.C. Lancet (1992) [Pubmed]
  14. Estrogen therapy for bleeding gastrointestinal telangiectasias. Brinberg, D., Green, P.H., Lebwohl, O. Ann. Intern. Med. (1986) [Pubmed]
  15. Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in fibroblasts from patients with Huntington disease, familial dysautonomia, and other primary neuronal degenerations. Scudiero, D.A., Meyer, S.A., Clatterbuck, B.E., Tarone, R.E., Robbins, J.H. Proc. Natl. Acad. Sci. U.S.A. (1981) [Pubmed]
  16. Mutations revealed by sequencing the 5' half of the gene for ataxia telangiectasia. Byrd, P.J., McConville, C.M., Cooper, P., Parkhill, J., Stankovic, T., McGuire, G.M., Thick, J.A., Taylor, A.M. Hum. Mol. Genet. (1996) [Pubmed]
  17. TEL1, a gene involved in controlling telomere length in S. cerevisiae, is homologous to the human ataxia telangiectasia gene. Greenwell, P.W., Kronmal, S.L., Porter, S.E., Gassenhuber, J., Obermaier, B., Petes, T.D. Cell (1995) [Pubmed]
  18. Functional link of BRCA1 and ataxia telangiectasia gene product in DNA damage response. Li, S., Ting, N.S., Zheng, L., Chen, P.L., Ziv, Y., Shiloh, Y., Lee, E.Y., Lee, W.H. Nature (2000) [Pubmed]
  19. An essential function for NBS1 in the prevention of ataxia and cerebellar defects. Frappart, P.O., Tong, W.M., Demuth, I., Radovanovic, I., Herceg, Z., Aguzzi, A., Digweed, M., Wang, Z.Q. Nat. Med. (2005) [Pubmed]
  20. A murine model of hereditary hemorrhagic telangiectasia. Bourdeau, A., Dumont, D.J., Letarte, M. J. Clin. Invest. (1999) [Pubmed]
  21. Defective potassium currents in ataxia telangiectasia fibroblasts. Rhodes, N., D'Souza, T., Foster, C.D., Ziv, Y., Kirsch, D.G., Shiloh, Y., Kastan, M.B., Reinhart, P.H., Gilmer, T.M. Genes Dev. (1998) [Pubmed]
  22. ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome. Curry, C.J., O'Lague, P., Tsai, J., Hutchison, H.T., Jaspers, N.G., Wara, D., Gatti, R.A., Hutchinson, H.T. Am. J. Hum. Genet. (1989) [Pubmed]
  23. Specificity of bleomycin-induced cytotoxic effects on ataxia telangiectasia lymphoid cell lines. Cohen, M.M., Simpson, S.J., Pazos, L. Cancer Res. (1981) [Pubmed]
  24. Atm-deficient mice Purkinje cells show age-dependent defects in calcium spike bursts and calcium currents. Chiesa, N., Barlow, C., Wynshaw-Boris, A., Strata, P., Tempia, F. Neuroscience (2000) [Pubmed]
  25. The pathology of acute hepatic disintegration in hereditary haemorrhagic telangiectasia. Blewitt, R.W., Brown, C.M., Wyatt, J.I. Histopathology (2003) [Pubmed]
  26. A checkpoint regulates the rate of progression through S phase in S. cerevisiae in response to DNA damage. Paulovich, A.G., Hartwell, L.H. Cell (1995) [Pubmed]
  27. The mei-41 gene of D. melanogaster is a structural and functional homolog of the human ataxia telangiectasia gene. Hari, K.L., Santerre, A., Sekelsky, J.J., McKim, K.S., Boyd, J.B., Hawley, R.S. Cell (1995) [Pubmed]
  28. Role of Nbs1 in the activation of the Atm kinase revealed in humanized mouse models. Difilippantonio, S., Celeste, A., Fernandez-Capetillo, O., Chen, H.T., Reina San Martin, B., Van Laethem, F., Yang, Y.P., Petukhova, G.V., Eckhaus, M., Feigenbaum, L., Manova, K., Kruhlak, M., Camerini-Otero, R.D., Sharan, S., Nussenzweig, M., Nussenzweig, A. Nat. Cell Biol. (2005) [Pubmed]
  29. Interaction of FANCD2 and NBS1 in the DNA damage response. Nakanishi, K., Taniguchi, T., Ranganathan, V., New, H.V., Moreau, L.A., Stotsky, M., Mathew, C.G., Kastan, M.B., Weaver, D.T., D'Andrea, A.D. Nat. Cell Biol. (2002) [Pubmed]
  30. The mouse genomic instability mutation chaos1 is an allele of Polq that exhibits genetic interaction with Atm. Shima, N., Munroe, R.J., Schimenti, J.C. Mol. Cell. Biol. (2004) [Pubmed]
  31. Nijmegen breakage syndrome. van der Burgt, I., Chrzanowska, K.H., Smeets, D., Weemaes, C. J. Med. Genet. (1996) [Pubmed]
  32. Idiopathic and radiation-induced ocular telangiectasia: the involvement of the ATM gene. Mauget-Faÿsse, M., Vuillaume, M., Quaranta, M., Moullan, N., Angèle, S., Friesen, M.D., Hall, J. Invest. Ophthalmol. Vis. Sci. (2003) [Pubmed]
  33. Treatment of essential telangiectasia: effects of increasing concentrations of polidocanol. Norris, M.J., Carlin, M.C., Ratz, J.L. J. Am. Acad. Dermatol. (1989) [Pubmed]
  34. Evaluation of the mouse mutant "wasted" as an animal model for ataxia telangiectasia. I. Age-dependent and tissue-specific effects. Tezuka, H., Inoue, T., Noguti, T., Kada, T., Shultz, L.D. Mutat. Res. (1986) [Pubmed]
  35. Painless cauterization of spider veins with the use of iontophoretic local anesthesia. Bezzant, J.L., Stephen, R.L., Petelenz, T.J., Jacobsen, S.C. J. Am. Acad. Dermatol. (1988) [Pubmed]
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