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Items: 5


Neurobiological mechanisms of pain in sickle cell disease.

Wang ZJ, Wilkie DJ, Molokie R.

Hematology Am Soc Hematol Educ Program. 2010;2010:403-8. doi: 10.1182/asheducation-2010.1.403.


Human globin knock-in mice complete fetal-to-adult hemoglobin switching in postnatal development.

McConnell SC, Huo Y, Liu S, Ryan TM.

Mol Cell Biol. 2011 Feb;31(4):876-83. doi: 10.1128/MCB.00725-10.


Regulation of iron absorption in hemoglobinopathies.

Rechavi G, Rivella S.

Curr Mol Med. 2008 Nov;8(7):646-62. Review.


Correction of the sickle cell mutation in embryonic stem cells.

Chang JC, Ye L, Kan YW.

Proc Natl Acad Sci U S A. 2006 Jan 24;103(4):1036-40.


Multiple interactions between regulatory regions are required to stabilize an active chromatin hub.

Patrinos GP, de Krom M, de Boer E, Langeveld A, Imam AM, Strouboulis J, de Laat W, Grosveld FG.

Genes Dev. 2004 Jun 15;18(12):1495-509.

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