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MeSH Review

Abnormalities, Multiple

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Disease relevance of Abnormalities, Multiple


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Biological context of Abnormalities, Multiple


Anatomical context of Abnormalities, Multiple


Gene context of Abnormalities, Multiple


Analytical, diagnostic and therapeutic context of Abnormalities, Multiple


  1. Differential transcriptional control as the major molecular event in generating Otx1-/- and Otx2-/- divergent phenotypes. Acampora, D., Avantaggiato, V., Tuorto, F., Barone, P., Perera, M., Choo, D., Wu, D., Corte, G., Simeone, A. Development (1999) [Pubmed]
  2. The germinal isozyme of angiotensin-converting enzyme can substitute for the somatic isozyme in maintaining normal renal structure and functions. Kessler, S.P., Gomos, J.B., Scheidemantel, T.S., Rowe, T.M., Smith, H.L., Sen, G.C. J. Biol. Chem. (2002) [Pubmed]
  3. Deletion of the Src homology 3 domain and C-terminal proline-rich sequences in Bcr-Abl prevents Abl interactor 2 degradation and spontaneous cell migration and impairs leukemogenesis. Dai, Z., Kerzic, P., Schroeder, W.G., McNiece, I.K. J. Biol. Chem. (2001) [Pubmed]
  4. Polycystic ovarian syndrome: evidence that flutamide restores sensitivity of the gonadotropin-releasing hormone pulse generator to inhibition by estradiol and progesterone. Eagleson, C.A., Gingrich, M.B., Pastor, C.L., Arora, T.K., Burt, C.M., Evans, W.S., Marshall, J.C. J. Clin. Endocrinol. Metab. (2000) [Pubmed]
  5. Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbances. van Ommen, C.H., Peters, M., Barth, P.G., Vreken, P., Wanders, R.J., Jaeken, J. J. Pediatr. (2000) [Pubmed]
  6. Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance. Kadowaki, T., Bevins, C.L., Cama, A., Ojamaa, K., Marcus-Samuels, B., Kadowaki, H., Beitz, L., McKeon, C., Taylor, S.I. Science (1988) [Pubmed]
  7. Clomid administration to pregnant rats causes abnormalities of the reproductive tract in offspring and mothers. McCormack, S., Clark, J.H. Science (1979) [Pubmed]
  8. BCR/ABL induces multiple abnormalities of cytoskeletal function. Salgia, R., Li, J.L., Ewaniuk, D.S., Pear, W., Pisick, E., Burky, S.A., Ernst, T., Sattler, M., Chen, L.B., Griffin, J.D. J. Clin. Invest. (1997) [Pubmed]
  9. An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect. Hayward, C.P., Rivard, G.E., Kane, W.H., Drouin, J., Zheng, S., Moore, J.C., Kelton, J.G. Blood (1996) [Pubmed]
  10. Evidence that an abnormality in the glycoprotein Ib alpha gene is not the cause of abnormal platelet function in a family with classic Bernard-Soulier disease. Finch, C.N., Miller, J.L., Lyle, V.A., Handin, R.I. Blood (1990) [Pubmed]
  11. Clomid or nafoxidine administered to neonatal rats causes reproductive tract abnormalities. Clark, J.H., McCormack, S. Science (1977) [Pubmed]
  12. Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants. Mendelsohn, C., Lohnes, D., Décimo, D., Lufkin, T., LeMeur, M., Chambon, P., Mark, M. Development (1994) [Pubmed]
  13. Microalbuminuria precedes the development of NIDDM. Mykkänen, L., Haffner, S.M., Kuusisto, J., Pyorälä, K., Laakso, M. Diabetes (1994) [Pubmed]
  14. Multiple abnormalities in insulin responses to nonglucose nutrients in neonatally streptozotocin diabetic rats. Grill, V., Sako, Y., Ostenson, C.G., Jalkanen, P. Endocrinology (1991) [Pubmed]
  15. Impaired glucose tolerance is characterized by multiple abnormalities in the regulation of intermediary metabolism. Krentz, A.J., Singh, B.M., Nattrass, M. Diabet. Med. (1991) [Pubmed]
  16. Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings. Bernstein, R., Jenkins, T., Dawson, B., Wagner, J., Dewald, G., Koo, G.C., Wachtel, S.S. J. Med. Genet. (1980) [Pubmed]
  17. Insulin resistance: a multifaceted metabolic syndrome. Insights gained using a low-dose insulin infusion technique. Krentz, A.J., Nattrass, M. Diabet. Med. (1996) [Pubmed]
  18. Human DNA topoisomerases II alpha and II beta can functionally substitute for yeast TOP2 in chromosome segregation and recombination. Jensen, S., Redwood, C.S., Jenkins, J.R., Andersen, A.H., Hickson, I.D. Mol. Gen. Genet. (1996) [Pubmed]
  19. Trisomy 16 in a mid-trimester IVF foetus with multiple abnormalities. Seller, M.J., Fear, C., Kumar, A., Mohammed, S. Clin. Dysmorphol. (2004) [Pubmed]
  20. Polydactyly and ectopic ZPA formation in Alx-4 mutant mice. Qu, S., Niswender, K.D., Ji, Q., van der Meer, R., Keeney, D., Magnuson, M.A., Wisdom, R. Development (1997) [Pubmed]
  21. Role of intestinal transit in the pathogenesis of gallbladder stones. Dowling, R.H., Veysey, M.J., Pereira, S.P., Hussaini, S.H., Thomas, L.A., Wass, J.A., Murphy, G.M. Can. J. Gastroenterol. (1997) [Pubmed]
  22. Dyskeratosis congenita: a disorder of defective telomere maintenance? Walne, A.J., Marrone, A., Dokal, I. Int. J. Hematol. (2005) [Pubmed]
  23. Neutrophils from patients with myelodysplastic syndromes: relationship between impairment of granular contents, complement receptors, functional activities and disease status. Moretti, S., Lanza, F., Spisani, S., Latorraca, A., Rigolin, G.M., Giuliani, A.L., Castoldi, G.L., Traniello, S. Leuk. Lymphoma (1994) [Pubmed]
  24. Abnormal vascular function and hypertension in mice deficient in estrogen receptor beta. Zhu, Y., Bian, Z., Lu, P., Karas, R.H., Bao, L., Cox, D., Hodgin, J., Shaul, P.W., Thoren, P., Smithies, O., Gustafsson, J.A., Mendelsohn, M.E. Science (2002) [Pubmed]
  25. Signalling molecules and cytokine production in T cells of multiple myeloma-increased abnormalities with advancing stage. Mozaffari, F., Hansson, L., Kiaii, S., Ju, X., Rossmann, E.D., Rabbani, H., Mellstedt, H., Osterborg, A. Br. J. Haematol. (2004) [Pubmed]
  26. Activation of the canonical Wnt/beta-catenin pathway confers growth advantages in c-Myc/E2F1 transgenic mouse model of liver cancer. Calvisi, D.F., Conner, E.A., Ladu, S., Lemmer, E.R., Factor, V.M., Thorgeirsson, S.S. J. Hepatol. (2005) [Pubmed]
  27. Surfactant metabolism in SP-D gene-targeted mice. Ikegami, M., Whitsett, J.A., Jobe, A., Ross, G., Fisher, J., Korfhagen, T. Am. J. Physiol. Lung Cell Mol. Physiol. (2000) [Pubmed]
  28. Wasp sting anaphylaxis. Ratnoff, O.D., Nossel, H.L. Blood (1983) [Pubmed]
  29. Multiple intron retention occurs in tumor cell CD44 mRNA processing. Goodison, S., Yoshida, K., Churchman, M., Tarin, D. Am. J. Pathol. (1998) [Pubmed]
  30. Technetium-99m MDP bone scintigraphy shows multiple abnormalities in sickle cell disease. Adams, B.K., Parkar, S., Al-Haider, Z.Y. Arch. Dis. Child. (2003) [Pubmed]
  31. Leuconostoc bacteremia in a child with short-gut syndrome. Helali, A., McAlear, D., Osoba, A. Saudi medical journal. (2005) [Pubmed]
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