Genomics of phage-bacterium-host interaction of mushroom pathogenic Pseudomonads Nathaniel Storey
Medical laboratory science examination review by OHANA - Issuu
An NLRP3 Mutation Causes Arthropathy and Osteoporosis in Humanized Mice
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Calcium metabolism in grey parrots - Harrison's Bird Foods
Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Bruton's Tyrosine Kinase ...
Marie Meurs-Gerken on Twitter: "Skadestuebesøg nr 2 veloverstået - vabel tacklet af fluffy duffy og gigant forbinding http://t.co/NAPoSqhZ" / Twitter
Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Bruton's Tyrosine Kinase ...
Primates, Pathogens, and Evolution
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Renal Diseases Associated with Hematopoietic Disorders or Organized Deposits (Chapter 11) - Silva's Diagnostic Renal Pathology
Apoproteins and Cell Surface Receptors Regulating Lipoprotein Metabolism in the Setting of Type 2 Diabetes | SpringerLink
Dual Effect of the Acidic Polysaccharose Ulvan on the Inhibition of Amyloid-β Protein Fibrillation and Disintegration of Mature Fibrils | ACS Applied Materials & Interfaces
Vegan Pancakes Recipe | One Ingredient Chef
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Infectious disease - Abstract - Europe PMC
The effect of direct amine substituted push–pull oligothiophene chromophores on dye-sensitized and bulk heterojunction solar cells performance - ScienceDirect
Synthesis, Structure, and Activity of Diclofenac Analogues as Transthyretin Amyloid Fibril Formation Inhibitors | Journal of Medicinal Chemistry
Invention of MK-8262, a Cholesteryl Ester Transfer Protein (CETP) Inhibitor Backup to Anacetrapib with Best-in-Class Properties | Journal of Medicinal Chemistry
![2S,3S)-3-Amino-4-(3,3-difluoropyrrolidin-1-yl)-N,N-dimethyl-4-oxo-2-(4-[1,2,4]triazolo[1,5-a]- pyridin-6-ylphenyl)butanamide: A Selective α-Amino Amide Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/jm060015t/asset/images/jm060015t.social.jpeg_v03 "2S,3S)-3-Amino-4-(3,3-difluoropyrrolidin-1-yl)-N,N-dimethyl-4-oxo-2-(4-[1,2,4]triazolo[1,5-a]- pyridin-6-ylphenyl)butanamide: A Selective α-Amino Amide Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes | Journal of Medicinal Chemistry")
2S,3S)-3-Amino-4-(3,3-difluoropyrrolidin-1-yl)-N,N-dimethyl-4-oxo-2-(4-[1,2,4]triazolo[1,5-a]- pyridin-6-ylphenyl)butanamide: A Selective α-Amino Amide Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes | Journal of Medicinal Chemistry
CXCL12 retargeting of an adenovirus vector to cancer cells using a bispecific adapter
Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Bruton's Tyrosine Kinase ...
Science - 2020 12 04
Neuromedin: An insight into its types, receptors and therapeutic opportunities
