Endocrine Manifestations of Chromosome 22q11.2 Microdeletion Syndrome

Identification of novel mutations of the DAX-1 gene in the patients with X-linked adrenal hypoplasia congenita (AHC)

Detection of maternal uniparental disomy at the two imprinted genes on chromosome 7, GRB10 and PEG1/MEST, in a Silver-Russell syndrome patient using methylation-specific PCR assays

Progressive hair loss and myocardial degeneration in rough coat mice: reduced LOXL expression in the skin and heart

Neutrophil Lactoferrin Upregulates the Human p53 Gene through Induction of NF-kB Activation Cascade

Clinical characteristics and molecular analysis of PIT1, PROP1, LHX3, and HESX1 in combined pituitary hormone deficiency patients with abnormal pitui

Expression and purification of enzymatically active forms of the human lysyl oxidase-like protein 4

PKCd-dependent cleavage and nuclear translocation of annexin A1 by phorbol 12-myristate 13-acetate

Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome

Purification of enzymatically active human lysyl oxidase (LOX) and lysyl oxidase-like protein (LOXL) from Escherichia coli inclusion bodies.