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Yves Sabbagh

Research Profile

Chemicals & Drugs

Disorders

Physiology

Anatomy

Living Beings

Mouse

Procedures

Biotinylation

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Publications

TOP 3
Yves Sabbagh; Guy Boileau; Marcelo Campos; Adriana K Carmona; Harriet S Tenenhouse
Structure and function of disease-causing missense mutations in the PHEX gene.
Harriet S Tenenhouse; Yves Sabbagh
Novel phosphate-regulating genes in the pathogenesis of renal phosphate wasting disorders.
D L Thompson; Yves Sabbagh; Harriet S Tenenhouse; P C Roche; Marc K Drezner; Jeffrey Salisbury; J P Grande; E M Poeschla; R Kumar
Ontogeny of Phex/PHEX protein expression in mouse embryo and subcellular localization in osteoblasts.

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All Publications

2003: Yves Sabbagh; Guy Boileau; Marcelo Campos; Adriana K Carmona; Harriet S Tenenhouse
Structure and function of disease-causing missense mutations in the PHEX gene.
The Journal of clinical endocrinology and metabolism 2003;88(5):2213-22.
2002: Harriet S Tenenhouse; Yves Sabbagh
Novel phosphate-regulating genes in the pathogenesis of renal phosphate wasting disorders.
Pflügers Archiv : European journal of physiology 2002;444(3):317-26.
2002: D L Thompson; Yves Sabbagh; Harriet S Tenenhouse; P C Roche; Marc K Drezner; Jeffrey Salisbury; J P Grande; E M Poeschla; R Kumar
Ontogeny of Phex/PHEX protein expression in mouse embryo and subcellular localization in osteoblasts.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2002;17(2):311-20.
2002: Yves Sabbagh; Claude Gauthier; Harriet S Tenenhouse
The X chromosome deletion in HYP mice extends into the intergenic region but does not include the SAT gene downstream from Phex.
Cytogenetic and genome research 2002;99(1-4):344-9.
2001: Yves Sabbagh; Guy Boileau; Luc DesGroseillers; Harriet S Tenenhouse
Disease-causing missense mutations in the PHEX gene interfere with membrane targeting of the recombinant protein.
Human molecular genetics 2001;10(15):1539-46.
2000: Yves Sabbagh; A O Jones; Harriet S Tenenhouse
PHEXdb, a locus-specific database for mutations causing X-linked hypophosphatemia.
Human mutation 2000;16(1):1-6.

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