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Molecular Cancer Research : MCR|August 27, 2021
NP-ALT, a Liposomal:Peptide Drug, Blocks p27Kip1 Phosphorylation to Induce Oxidative Stress, Necroptosis, and Regression in Therapy-Resistant Breast Cancer CellsIrina Jilishitz, Jason Luis Quiñones, Priyank Patel, et al.
The Journal of Clinical Endocrinology and Metabolism|October 12, 2021
Sustained Efficacy and Safety of Burosumab, a Monoclonal Antibody to FGF23, in Children With X-Linked HypophosphatemiaAgnès Linglart, Erik A Imel, Michael P Whyte, et al.
Bone|December 28, 2020
Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type VMichael P Whyte, James Aronson, William H McAlister, et al.
Bone|September 1, 2019
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutationSteven Mumm, Gary S Gottesman, Deborah Wenkert, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
Pathogenic strains of a gut commensal drive systemic platelet activation and thromboinflammation in lupus nephritisAbhimanyu Amarnani, Cristobal F Rivera, Macintosh Cornwell, et al.
Molecular Genetics and Metabolism|April 18, 2006
Enhancement of drug delivery to bone: characterization of human tissue-nonspecific alkaline phosphatase tagged with an acidic oligopeptideTatsuo Nishioka, Shunji Tomatsu, Monica A Gutierrez, et al.
Bone|May 17, 2021
Vitamin B6 deficiency with normal plasma levels of pyridoxal 5'-phosphate in perinatal hypophosphatasiaMichael P Whyte, Jennifer D May, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 4, 2003
Marrow cell transplantation for infantile hypophosphatasiaMichael P Whyte, Joanne Kurtzberg, William H McAlister, et al.
Annals of the Rheumatic Diseases|April 24, 2026
A pathogenic gut lipoglycan drives systemic thromboinflammation in lupus nephritisAbhimanyu Amarnani, Cristobal F Rivera, Macintosh Cornwell, et al.
Bone|November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
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