Paul T. Christie
Oxford, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Genetic background influences tumour development in heterozygous Men1 knockout mice.
Journal: Endocrine connections
Published: April 17, 2020
Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism.
Journal: Endocrine connections
Published: December 19, 2019
An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: June 10, 2018
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: April 20, 2018
Pseudohypoparathyroidism type 1a due to a novel mutation in the GNAS gene.
Journal: Clinical endocrinology
Published: September 25, 2015
GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasiveness.
Journal: Hormones & cancer
Published: January 02, 2013
MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomas.
Journal: Cancer research
Published: August 24, 2012
Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 03, 2012
Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites.
Journal: Human molecular genetics
Published: March 17, 2012
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Last Updated: 09/26/2026