Increased rate of gluconeogenesis in type II diabetes mellitus. A 13C nuclear magnetic resonance study.

I Magnusson, Douglas L. Rothman, Lee D. Katz, +2

Journal of Clinical Investigation

Glucose Metabolism and Regulation: Beyond Insulin and Glucagon

Stephen Aronoff, Kathy J. Berkowitz, Barb Shreiner, +1

Diabetes Spectrum

Metabolic SyndromeInsulin SignalingDiabetes ManagementBiochemistryInsulin Management +12

Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1

Lygia V. Pereira, Sui Ying Lee, Barbara Gayraud-Morel, +7

Proceedings of the National Academy of Sciences

A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome.

Dianna M. Milewicz, Joseph Grossfield, Shinuo Cao, +3

Journal of Clinical Investigation

Marfan SyndromeFibrosisDevelopmental BiologyMendelian DisorderGenetic Disorder +10

Seipin ablation in mice results in severe generalized lipodystrophy

Xin Cui, Yan Wang, Yuhan Tang, +7

Human Molecular Genetics

Biochemistry of the Protein Hormones

O K Behrens, William Bromer

Annual Review of Biochemistry

Tissue GrowthOrgan DevelopmentCell GrowthCellular PhysiologyDrosophila Melanogaster +19

The Triterpenoid 2-Cyano-3,12-dioxooleana-1,9-dien-28-oic-acid Methyl Ester Has Potent Anti-diabetic Effects in Diet-induced Diabetic Mice and Lepr Mice

Pradip Saha, Vasumathi T. Reddy, Marina Konopleva, +2

Journal of Biological Chemistry

Marfan syndrome with neonatal progeroid syndrome‐like lipodystrophy associated with a novel frameshift mutation at the 3′ terminus of the <i>FBN1</i>‐gene

Luitgard Graul‐Neumann, Tina Kienitz, Peter N. Robinson, +7

American Journal of Medical Genetics Part A

Evidence for furin-type activity-mediated C-terminal processing of profibrillin-1 and interference in the processing by certain mutations

Lasse Lönnqvist

Human Molecular Genetics

Severe congenital lipodystrophy and a progeroid appearance: Mutation in the penultimate exon of <i>FBN1</i> causing a recognizable phenotype

Toshiki Takenouchi, Mariko Hida, Yoshiaki Sakamoto, +4

American Journal of Medical Genetics Part A