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Refined by: collection: MEDLINE/PubMed (NLM) remove material type: Articles remove journal title: Blood remove
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Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD.

Blood, October 13, 2016, Vol.128(15), pp.1979-1986 [Peer Reviewed Journal]

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Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.

Blood, June 23, 2016, Vol.127(25), pp.3154-3164 [Peer Reviewed Journal]

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Severe chronic primary neutropenia in adults: report on a series of 108 patients.

Blood, October 1, 2015, Vol.126(14), pp.1643-1650 [Peer Reviewed Journal]

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A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation.

Blood, November 3, 2011, Vol.118(18), pp.4798-4807 [Peer Reviewed Journal]

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New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein.

Blood, July 28, 2011, Vol.118(4), pp.926-935 [Peer Reviewed Journal]

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In vitro proliferation and differentiation of erythroid progenitors from patients with myelodysplastic syndromes: evidence for Fas-dependent apoptosis.

Blood, March 1, 2002, Vol.99(5), pp.1594-1601 [Peer Reviewed Journal]

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