Gloriosa Go

Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes

S. Young, Jennifer M. Gardner, L. Fong, 2007, Human mutation.

Laminin β2 gene missense mutation produces endoplasmic reticulum stress in podocytes.

Y. Kikkawa, Yuefang Zhou, J. Miner, 2013, Journal of the American Society of Nephrology : JASN.

Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation

A. Sutherland, J. Miner, Cong Li, 2004, Development.

Discs-large homolog 1 regulates smooth muscle orientation in the mouse ureter

R. Xavier, W. Swat, B. Sammut, 2006, Proceedings of the National Academy of Sciences.

Feasibility of repairing glomerular basement membrane defects in Alport syndrome.

J. Miner, J. Suh, Gloriosa Go, 2014, Journal of the American Society of Nephrology : JASN.

Induction of lambdoid prophages by amino acid deprivation: Differential inducibility; Role of recA

Gloriosa Go, N. E. Melechen, 2004, Molecular and General Genetics MGG.

Effect of cI repressor level on thymineless and spontaneous induction; Specificity of lambda RNA transcription

Gloriosa Go, H. Lozeron, N. E. Melechen, 1978, Molecular and General Genetics MGG.

Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy.

Jennifer M. Gardner, A. C. van der Wal, J. Miner, 2005, The Journal of investigative dermatology.

Transgenic isolation of skeletal muscle and kidney defects in lamininβ 2 mutant mice: implications for Pierson syndrome

J. Miner, G. Jarad, B. Patton, 2006, Development.