ライフサイエンスコーパス: Adams

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1 Adams et al. in this issue of Immunity provide evidence

2 Adams-Oliver syndrome (AOS) is a rare developmental diso

3 Adams-Oliver syndrome (AOS) is a rare disorder character

4 pply evolved magmas to Mounts St. Helens and Adams, and possibly Rainier, and could contain approxima

5 ade before her language deficits arose, Anne Adams (AA), a lifelong scientist, developed an intense d

6 In an accompanying article, Adams et al. used a subsample of the National Institutes

7 In this issue of Blood, Adams et al provide evidence for an important novel func

8 Therefore, both Adams and the miR-29 family represent therapeutic target

9 BPJ) in two independent families affected by Adams-Oliver syndrome (AOS), a rare multiple-malformatio

10 See related article by Adams et al., Cancer Res 1999;59:2615-22Visit the Cancer

11 sumer expenditures for alcohol, published by Adams Business Research.

12 tigated a recognized developmental disorder, Adams-Oliver syndrome (AOS), characterized by the combin

13 but mesotrione-sensitive population (ACR for Adams County mesotrione-sensitive but atrazine-resistant

14 ghly cited 1999 Cancer Research article from Adams and colleagues was published during the period whe

15 Helens, Adams, and Rainier these pathways connect subduction-ind

16 (i) gain-of-function CdGAP mutants found in Adams-Oliver Syndrome patients strongly destabilize cell

17 model renal fibrosis, we observed increased Adams gene expression that was blocked by oral administr

18 Jean Adams and colleagues argue that population interventions

19 The Carpentier-McCarthy-Adams (CMA) IMR ETlogix annuloplasty ring is the first r

20 e melt source region lies east towards Mount Adams.

21 ls results in a significant up-regulation of Adams 10, 17, 12, and 19.

22 ic Reactions and the initiation of the Roger Adams Award are discussed.

23 This study shows that Adams are involved in renal fibrosis and are regulated b

24 al solute concentration that incorporate the Adams-Fujita assumption for composition-dependence of ac

25 OTCH1 variants in unrelated individuals with Adams-Oliver syndrome (AOS), a rare disease with major f

26 posed by a father and two affected sibs with Adams Oliver syndrome (AOS) (OMIM 100300).

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