SFX by Ex Libris Inc.

Title:	Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults
Source:	Molecular Biology Reports [0301-4851] Jouini, Latifa yr:2011

Basic

Full text

Full text available via SpringerLINK Contemporary 1997-Present

Year:

Volume:

Issue:

Start Page:

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Smith, Elenoe C. "Hemoglobin genetics: recent contributions of GWAS and gene editing." Human molecular genetics 25.R2 (2016).
description	2.	Mtatiro, Siana N. "Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania." PLoS ONE 9.11 (2014).
description	3.	WHITE, J C. "Foetal Haemoglobin." British Medical Bulletin 15.1 (1959): 33-9.
description	4.	de Vasconcellos, Jaira F. "LIN28A Expression Reduces Sickling of Cultured Human Erythrocytes." PLoS ONE 9.9 (2014).
description	5.	MartÃ-Carvajal, Arturo J. "Interventions for treating leg ulcers in people with sickle cell disease." Cochrane Database of Systematic Reviews 11.12 (2012).
description	6.	Timmann, C. "Genome-wide association study indicates two novel resistance loci for severe malaria." Nature 489.7416 (2012): 443-446.
description	7.	Lodish, Harvey A. "Gene induction and repression during terminal erythropoiesis are mediated by distinct epigenetic changes." Blood 118.16 (2011): 128-38.
description	8.	Bulger, M. "Conservation of sequence and structure flanking the mouse and human beta-globin loci: The beta-globin genes are embedded within an array of odorant receptor genes." Proceedings of the National Academy of Sciences of the United States of America 96.9 (1999): 5129-5134.
description	9.	Volpe, Thomas A A. "Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi." Science 297.5588 (2002): 1833-7.
description	10.	Tawil, M. "Sickle cell leg ulcers: a frequently disabling complication and a marker of severity." British journal of dermatology 158.2 (2008): 339-44.
description	11.	Lena, L. "Foetal haemoglobin and disease severity in sickle cell anaemia patients in Kampala, Uganda." BMC Blood Disorders 12.1 (2012): 11-11.
description	12.	Khan, Muhammad A. "Reversal of hepatic and renal failure from sickle cell intrahepatic cholestasis." Digestive diseases and sciences 56.6 (2011): 1634-1636.
description	13.	Ladizinski B, B. "Sickle cell disease and leg ulcers." Advances in Skin & Wound Care 25.9 (2012): 429-430.
description	14.	Grewal, Shiv I S I. "RNAi-independent heterochromatin nucleation by the stress-activated ATF/CREB family proteins." Science 304.5679 (2004): 1971-6.
description	15.	Lippman, Z. "The role of RNA interference in heterochromatic silencing." Nature 431.7006 (2004): 364-70.
description	16.	Verdel, A. "RNAi-mediated targeting of heterochromatin by the RITS complex." Science 303.5658 (2003): 672-6.
description	17.	"Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster." Hemoglobin. 46.3: 168-175.
description	18.	Krivega, I. "Chromatin looping as a target for altering erythroid gene expression." Annals of the New York Academy of Sciences 13681.1 (2016): 31-39.
description	19.	Kadima, Bertin T. "High rate of sickle cell anaemia in Sub-Saharan Africa underlines the need to screen all children with severe anaemia for the disease." Acta paediatrica 104.12 (2015): 1269-73.
description	20.	Khoriaty, E. "Incidence of sickle cell disease and other hemoglobin variants in 10,095 lebanese neonates." PLoS ONE 9.9 (2014).