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1 Ninety-one percent of donors were blood group O.
2 an blood samples from adults and newborns of blood groups O, A, and B were treated with either anti-A
3 0.27-0.70) of type 2 diabetes compared with blood group O, adjusting for sE-selectin, sICAM-1, TNF-R
6 previously frozen plasma (four units each of blood group O and A), which can be issued immediately fo
7 f blood group A2 kidneys (20% of group A) to blood group O and B patients expands their potential don
8 the allocation of blood group A2 kidneys for blood group O and B recipients is a practical way to exp
9 nsplantation within 30 days for infants with blood group O and may benefit a broader range of transpl
10 is demonstrated that the association between blood group O and protection from infection with V. chol
11 is for understanding the association between blood group O and the risk of infection with V. cholerae
13 risk factor for bleeding in combination with blood group O and/other unknown genetic factors, and (3)
14 rmediate rate (30%) among secretors with non-blood group O, and the highest rate (51%) among secretor
19 ison with the frameshift deletion underlying blood group O: case-control allelic odds ratio (OR), 1.2
21 to the Globo H hexaglycosylceramide, i.e. a blood group O determinant on a type 4 core chain, the ge
22 abA-expressing H. pylori strains bind to the blood group O determinants on type 1 core chains, i.e. t
23 iver/small intestinal transplantation with a blood group O donor to a blood type A recipient is descr
24 ood group compatible donors, 100 consecutive blood group O donors, or ten highly selected homozygous
26 ssociated with severe malaria, is reduced in blood group O erythrocytes compared with groups A, B, an
28 th VWF:RCo < 50 U/dL (< 40 for patients with blood group O) fulfilled the acquired von Willebrand syn
31 n the transplant team preferentially selects blood group O living donors and cadaveric kidney allocat
32 candidates will not be affected adversely if blood group O living donors are selected preferentially
35 mic equivalents [gEq]) for secretor-positive blood group O or A persons and 7.0 (approximately 2800 g
40 ferase-deficient enzyme that encodes the ABO blood group O phenotype previously proposed to protect a
41 were isolated from the small intestine of a blood group O pig and characterized by mass spectrometry
43 el was associated with high SES, white race, blood group O, private insurance, and residence in regio
45 ransplantation of blood group A2 livers into blood group O recipients is safe and can be performed wi
46 ered more transplant opportunities to women, blood group O recipients, retransplants, and older patie
47 ped to avoid increasing the waiting time for blood group O recipients, we would support the implement
48 was significantly greater in volunteers with blood group O than those with non-O blood types (10,353
50 e samples were collected from a patient with blood group O undergoing antibody removal and subsequent
51 proposal would disadvantage cadaveric kidney blood group O wait list candidates, and present an appro
53 made the novel observation that persons with blood group O were less likely than those with other blo
54 or studies, however, household contacts with blood group O were more likely to develop severe illness
55 with each group including 2 volunteers with blood group O, were given a dose of 10(5) CFU, and 34 of
56 ible adult patients (aged >/= 18 years) with blood group O+, who required up to two whole blood unit
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