Alkaline Phosphatase and Hypophosphatasia

Por Millán, José Luis, Whyte, Michael P.
Publicado no Calcif Tissue Int (2015)

Camurati-Engelmann Disease: Unique Variant Featuring a Novel Mutation in TGFβ1 Encoding Transforming Growth Factor Beta 1 and a Missense Change in TNFSF11 Encoding RANK Ligand

Por Whyte, Michael P, Totty, William G, Novack, Deborah V, Zhang, Xiafang, Wenkert, Deborah, Mumm, Steven
Publicado em 2011

Juvenile Paget’s Disease In An Iranian Kindred With Vitamin D Deficiency And Novel Homozygous TNFRSF11B Mutation

Por Saki, Forough, Karamizadeh, Zohreh, Nasirabadi, Shiva, Mumm, Steven, McAlister, William H., Whyte, Michael P.
Publicado em 2013

Outcome of Perinatal Hypophosphatasia in Manitoba Mennonites: A Retrospective Cohort Analysis

Por Leung, Edward C. W., Mhanni, Aizeddin A., Reed, Martin, Whyte, Michael P., Landy, Hal, Greenberg, Cheryl R.
Publicado em 2013

Congenital Insensitivity To Pain: Fracturing Without Apparent Skeletal Pathobiology Caused By An Autosomal Dominant, Second Mutation in SCN11A Encoding Voltage-Gated Sodium Channel...

Por Phatarakijnirund, Voraluck, Mumm, Steven, McAlister, William H., Novack, Deborah, Wenkert, Deborah, Clements, Karen L., Whyte, Michael P.
Publicado no Bone (2015)

Auricular Ossification: A Newly Recognized Feature of Osteoprotegerin-Deficiency Juvenile Paget Disease

Por Gottesman, Gary S., Madson, Katherine L., McAlister, William H., Nenninger, Angela, Wenkert, Deborah, Mumm, Steven, Whyte, Michael P.
Publicado no Am J Med Genet A (2016)

Idiopathic Acquired Osteosclerosis In A Middle-aged Woman With Systemic Lupus Erythematosus

Por Guañabens, Núria, Mumm, Steven, Gifre, Laia, Gaspà, Silvia Ruiz, Demertzis, Jennifer L., Stolina, Marina, Novack, Deborah V., Whyte, Michael P
Publicado no J Bone Miner Res (2016)

Autosomal Recessive Hypophosphatasia Manifesting in Utero with Long Bone Deformity but Showing Spontaneous Postnatal Improvement

Por Stevenson, David A., Carey, John C., Coburn, Stephen P., Ericson, Karen L., Byrne, Janice L. B., Mumm, Steven, Whyte, Michael P.
Publicado em 2008

Dysosteosclerosis Presents as an “Osteoclast-Poor” Form of Osteopetrosis: Comprehensive Investigation of a 3-Year-Old Girl and Literature Review

Por Whyte, Michael P, Wenkert, Deborah, McAlister, William H, Novack, Deborah V, Nenninger, Angie R, Zhang, Xiafang, Huskey, Margaret, Mumm, Steven
Publicado em 2010

Juvenile Paget’s Disease With Heterozygous Duplication In TNFRSF11A Encoding RANK

Por Whyte, Michael P., Tau, Cristina, McAlister, William H., Zhang, Xiafang, Novack, Deborah V., Preliasco, Virginia, Santini-Araujo, Eduardo, Mumm, Steven
Publicado em 2014

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

Por Whyte, Michael P., Rockman-Greenberg, Cheryl, Ozono, Keiichi, Riese, Richard, Moseley, Scott, Melian, Agustin, Thompson, David D., Bishop, Nicholas, Hofmann, Christine
Publicado no J Clin Endocrinol Metab (2016)

Upregulation of Elastase Activity in Aorta in Mucopolysaccharidosis I and VII Dogs May be Due to Increased Cytokine Expression

Por Metcalf, Jason A., Linders, Bruce, Wu, Susan, Bigg, Paul, O’Donnell, Patricia, Sleeper, Meg M., Whyte, Michael P., Haskins, Mark, Ponder, Katherine P.
Publicado em 2009

Pathogenesis of lumbar spine disease in mucopolysaccharidosis VII

Por Smith, Lachlan J, Baldo, Guilherme, Wu, Susan, Liu, Yuli, Whyte, Michael P, Giugliani, Roberto, Elliott, Dawn M, Haskins, Mark E, Ponder, Katherine P
Publicado em 2012

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences:...

Por Hannan, Fadil M, Nesbit, M Andrew, Turner, Jeremy J O, Stacey, Joanna M, Cianferotti, Luisella, Christie, Paul T, Conigrave, Arthur D, Whyte, Michael P, Thakker, Rajesh V
Publicado em 2010

Dose response of bone-targeted enzyme replacement for murine hypophosphatasia

Por Yadav, Manisha C., Lemire, Isabelle, Leonard, Pierre, Boileau, Guy, Blond, Laurent, Beliveau, Martin, Cory, Esther, Sah, Robert L., Whyte, Michael P., Crine, Philippe, Millán, José Luis
Publicado em 2011

Multicentric Carpotarsal Osteolysis Syndrome is Caused by Only a Few Domain-Specific Mutations in MAFB, a Negative Regulator of RANKL-Induced Osteoclastogenesis

Por Mumm, Steven, Huskey, Margaret, Duan, Shenghui, Wenkert, Deborah, Madson, Katherine L., Gottesman, Gary S., Nenninger, Angela R., Laxer, Ronald M., McAlister, William H., Whyte, Michael P.
Publicado no Am J Med Genet A (2014)

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

Por Bowl, Michael R., Nesbit, M. Andrew, Harding, Brian, Levy, Elaine, Jefferson, Andrew, Volpi, Emanuela, Rizzoti, Karine, Lovell-Badge, Robin, Schlessinger, David, Whyte, Michael P., Thakker, Rajesh V.
Publicado em 2005

Enzyme replacement prevents enamel defects in hypophosphatasia mice

Por Yadav, Manisha C., de Oliveira, Rodrigo Cardoso, Foster, Brian L., Fong, Hanson, Cory, Esther, Narisawa, Sonoko, Sah, Robert L., Somerman, Martha, Whyte, Michael P., Millán, José Luis
Publicado em 2012

Alkaline Phosphatase Knock-Out Mice Recapitulate the Metabolic and Skeletal Defects of Infantile Hypophosphatasia

Por FEDDE, KENTON N., BLAIR, LIBBY, SILVERSTEIN, JULIE, COBURN, STEPHEN P., RYAN, LAWRENCE M., WEINSTEIN, ROBERT S., WAYMIRE, KATRINA, NARISAWA, SONOKO, MILLÁN, JOSÉ L., MACGREGOR, GRANT R., WHYTE, MICHAEL P.
Publicado em 1999

Rapid Skeletal Turnover In A Radiographic Mimic Of Osteopetrosis

Por Whyte, Michael P., Madson, Katherine L., Mumm, Steven, McAlister, William H., Novack, Deborah V., Blair, Jo C., Helliwell, Timothy R., Stolina, Marina, Abernethy, Laurence J., Shaw, Nicholas J.
Publicado no J Bone Miner Res (2014)