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A Pathogenetic Role for TNFα in the Syndrome of Cachexia, Arthritis, and Autoimmunity Resulting from Tristetraprolin (TTP) Deficiency
Results from the International Conference of Experts on Intra-abdominal Hypertension and Abdominal Compartment Syndrome. I. Definiti...
Direct neural fate specification from embryonic stem cells: a primitive mammalian neural stem cell stage acquired through a default ...
Platelet‐rich plasma and bovine porous bone mineral combined with guided tissue regeneration in the treatment of intrabony defects ...
MEK kinase 1 gene disruption alters cell migration and c-Jun NH2-terminal kinase regulation but does not cause a measurable defect i...
The 2008 National Institute of Child Health and Human Development Workshop Report on Electronic Fetal Monitoring: Update on Definiti...
A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficien...
Identification of a meristem L1 layer-specific gene in Arabidopsis that is expressed during embryonic pattern formation and defines ...
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumours and mismatch repair-defectiv...
Re: Viberg H, et al. Neurobehavioral derangements in adult mice receiving decabrominated diphenyl ether (PBDE 209) during a defined ...