Below are the most recent publications written about "Hemoglobinopathies" by people in Profiles.
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M?tais JY, Doerfler PA, Mayuranathan T, Bauer DE, Fowler SC, Hsieh MM, Katta V, Keriwala S, Lazzarotto CR, Luk K, Neel MD, Perry SS, Peters ST, Porter SN, Ryu BY, Sharma A, Shea D, Tisdale JF, Uchida N, Wolfe SA, Woodard KJ, Wu Y, Yao Y, Zeng J, Pruett-Miller S, Tsai SQ, Weiss MJ. Genome editing of HBG1 and HBG2 to induce fetal hemoglobin. Blood Adv. 2019 11 12; 3(21):3379-3392.
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Pederson T. The Hemoglobinopathies: An Empowering Era of Human Genetics in the Clinic and the Laboratory. FASEB J. 2017 09; 31(9):3711.
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Sahai I, Marsden D. Newborn screening. Crit Rev Clin Lab Sci. 2009; 46(2):55-82.
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Sankaran VG, Menne TF, Xu J, Akie TE, Lettre G, Van Handel B, Mikkola HK, Hirschhorn JN, Cantor AB, Orkin SH. Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A. Science. 2008 Dec 19; 322(5909):1839-42.
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Memtsoudis SG, Lekowski RW, Rosenberger P, Khalpey Z, FitzGerald DJ, Claypoole V, Courtney KD, Landzberg MJ, Bunn HF, Shekar PS. Pulmonary thrombectomy in a patient with hemoglobin Nottingham. Perfusion. 2007 Jul; 22(4):299-301.
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Wille RT, Krishnan K, Cooney KA, Bach DS, Martinez F. Familial association of primary pulmonary hypertension and a new low-oxygen affinity beta-chain hemoglobinopathy, Hb Washtenaw. Chest. 1996 Mar; 109(3):848-50.
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Krishnan K, Martinez F, Wille RT, Jones RT, Shih DT, Head C, Fairbanks VF, Dabich L. Hb Washtenaw [ beta 11(A8)Val-->Phe]: an electrophorectically silent, unstable, low oxygen affinity variant associated with anemia and chronic cyanosis. Hemoglobin. 1994 Sep; 18(4-5):285-95.