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Blood|July 3, 2010
Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell traitJeffrey J Swensen, Archana M Agarwal, Jose M Esquilin, et al.British Journal of Haematology|June 14, 2016
Clinical utility of next-generation sequencing in the diagnosis of hereditary haemolytic anaemiasArchana M Agarwal, Roberto H Nussenzveig, Noel S Reading, et al.Science (New York, N.Y.)|May 15, 2010
Genetic evidence for high-altitude adaptation in TibetTatum S Simonson, Yingzhong Yang, Chad D Huff, et al.Haematologica|June 14, 2006
Endothelin-1, vascular endothelial growth factor and systolic pulmonary artery pressure in patients with Chuvash polycythemiaVladimir I Bushuev, Galina Y Miasnikova, Adelina I Sergueeva, et al.Health and Quality of Life Outcomes|April 13, 2019
Development of a symptom assessment in patients with myelofibrosis: qualitative study findingsRuben A Mesa, Yun Su, Adrien Woolfson, et al.Leukemia Research|September 22, 2017
A phase 1 study of the Janus kinase 2 (JAK2)V617F inhibitor, gandotinib (LY2784544), in patients with primary myelofibrosis, polycythemia vera, and essential thrombocythemiaSrdan Verstovsek, Ruben A Mesa, Mohamed E Salama, et al.Gait & Posture|November 29, 2005
Induced acceleration contributions to locomotion dynamics are not physically well definedGeorge ChenBlood Advances|January 26, 2026
Ropeginterferon alfa-2b has minimal transplacental passage and breastmilk secretion in pregnant MPN patientsTsewang Tashi, Lee-Yung Shih, Yi-Te Yo, et al.Leukemia|May 12, 2018
Autocrine Tnf signaling favors malignant cells in myelofibrosis in a Tnfr2-dependent fashionWilliam L Heaton, Anna V Senina, Anthony D Pomicter, et al.British Journal of Haematology|May 29, 2010
Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemiaMehdi Nouraie, Noel S Reading, Andrew Campbell, et al.Pageof 29