Mouse knockout solves endocrine puzzle and promotes new pituitary lineage model
Open Access
- 15 March 2003
- journal article
- editorial
- Published by Cold Spring Harbor Laboratory in Genes & Development
- Vol. 17 (6) , 677-682
- https://doi.org/10.1101/gad.1085903
Abstract
No abstract availableThis publication has 69 references indexed in Scilit:
- Tbx1is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancerGenes & Development, 2003
- Variations on a ‘T’: orchestration of T-box signalling in developmentTrends in Genetics, 2002
- Tbx3 impinges on the p53 pathway to suppress apoptosis, facilitate cell transformation and block myogenic differentiationOncogene, 2002
- Alan Wolffe (1959–2001)Cell, 2001
- A Single Pitx1 Binding Site Is Essential for Activity of the LH Promoter in Transgenic MiceMolecular Endocrinology, 2001
- Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasiaHuman Molecular Genetics, 2001
- Heritable Disorders of Pituitary DevelopmentJournal of Clinical Endocrinology & Metabolism, 1999
- Mutations in PROP1 cause familial combined pituitary hormone deficiencyNature Genetics, 1998
- Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1Nature, 1990
- Heterogeneity of Ion Exchange ResinsScience, 1960