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1 s strongly correlated with neurohormonal and immune abnormalities.
2 to AIDS, organ transplantation or congenital immune abnormalities.
3 ment strategy to compensate for these innate immune abnormalities.
4 t is characterized by serologic and cellular immune abnormalities and is dependent on the presence of
5 ck of or defective hematopoietic stem cells, immune abnormalities, and disorders of the bone marrow m
6 fants may be capable of producing thymic and immune abnormalities, as suggested by previous reports o
7 odels of lupus has provided insight into the immune abnormalities associated with autoantibody produc
8 ment of barrier abnormalities and downstream immune abnormalities during the elicitation phase of mur
9 pic march." Controversy exists as to whether immune abnormalities, epidermal barrier defects, or both
10 he immune system, as evidenced by the severe immune abnormalities exhibited by patients bearing inact
12 and anxiety-like behaviors, suggesting that immune abnormalities in MIA offspring can contribute to
13 rointestinal tract and to define the mucosal immune abnormalities in patients with and without sympto
16 ormation will help to elucidate the cellular immune abnormalities leading to production of pathogenic
22 background AD might be explained by baseline immune abnormalities, such as increased TH2, TH17, and n
23 /TSP and underlie many of the characteristic immune abnormalities, such as spontaneous lymphocyte pro
24 rder (PTSD) is associated with endocrine and immune abnormalities that could increase risk for autoim
25 how that if immune biomarkers exist for such immune abnormality, they may be found in raised macropha
27 er p21 Ras oncoproteins by causing selective immune abnormalities without general developmental defec
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