Homocysteine stability in heparinized plasma stored in a gel separator tube.

نویسندگان

  • Roger R Calam
  • Ibrahim Mansoor
  • James Blaga
چکیده

References 1. Takahashi M, Buma Y, Iwamoto T, Inaguma Y, Ikeda H, Hiai H. Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains. Oncogene 1988;3:571–8. 2. Takahashi M, Buma Y, Hiai H. Isolation of ret proto-oncogene cDNA with an amino-terminal signal sequence. Oncogene 1989;4:805–6. 3. Airaksinen MS, Saarma M. The GDNF family: signalling, biological functions and therapeutic value. Nat Rev Neurosci 2002;3:383–94. 4. Amiel J, Lyonnet S. Hirschsprung disease, associated syndromes, and genetics: a review. J Med Genet 2001;38:729–39. 5. Chakravarti A, Lyonnet S. Hirschsprung disease. In: Scriver CR, Sly WS, Childs B, Beaudet AL, Valle D, Kinzler KW, Vogelstein B. The metabolic and molecular bases of inherited disease, 8th ed. New York: McGraw-Hill, 2001:6231–55. 6. Parisi MA, Kapur RP. Genetics of Hirschsprung disease. Curr Opin Pediatr 2000;12:610–7. 7. Iwashita T, Murakami H, Asai N, Takahashi M. Mechanism of ret dysfunction by Hirschsprung mutations affecting its extracellular domain. Hum Mol Genet 1996;5:1577–80. 8. Pelet A, Geneste O, Edery P, Pasini A, Chappuis S, Attie T, et al. Various mechanisms cause RET-mediated signaling defects in Hirschsprung’s disease. J Clin Invest 1998;101:1415–23. 9. Cosma M, Cardone M, Carlomagno F, Colantuoni V. Mutations in the extracellular domain cause RET loss of function by a dominant negative mechanism. Mol Cell Biol 1998;18:3321–9. 10. Geneste O, Biduad C, De Vita G, Hofstra R, Tartare-Deckert S, Buys C, et al. Two distinct mutations of the RET receptor causing Hirschsprung’s disease impair the binding of signalling effectors to a multifunctional docking site. Hum Mol Genet 1999;8:1989–99. 11. Iwashita T, Kurokawa K, Qiao S, Murakami H, Asai N, Kawai K, et al. Functional analysis of RET with Hirschsprung mutations affecting its kinase domain. Gastroenterology 2001;121:24–33. 12. Pasini B, Borrello M, Greco A, Bongarzone I, Luo Y, Mondellini P, et al. Loss of function effect of RET mutations causing Hirschsprung disease. Nat Genet 1995;10:35–40. 13. Garcia-Barceló M, Sham MH, Lui VCH, Chen BLS, Tam PKH. Analysis of the RET, GDNF, EDNRB and EDN3 genes in Chinese Hirschsprung’s patients. Clin Chem 2004;50:93–100. 14. Tam PK, Garcia-Barceló M. Molecular genetics of Hirschsprung’s disease. Semin Pediatr Surg 2004;3:236–48.

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عنوان ژورنال:
  • Clinical chemistry

دوره 51 8  شماره 

صفحات  -

تاریخ انتشار 2005