Cargando…

Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy

Albright hereditary osteodystrophy (AHO) is caused by heterozygous inactivation of GNAS, a complex locus that encodes the alpha‐stimulatory subunit of heterotrimeric G proteins (Gsα) in addition to NESP55 and XLαs due to alternative first exons. AHO skeletal manifestations include brachydactyly, bra...

Descripción completa

Detalles Bibliográficos
Autores principales:	McMullan, Patrick, Maye, Peter, Yang, Qingfen, Rowe, David W., Germain‐Lee, Emily L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2021
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771002/ https://www.ncbi.nlm.nih.gov/pubmed/35079678 http://dx.doi.org/10.1002/jbm4.10570

Ejemplares similares

Heterotopic Ossifications in a Mouse Model of Albright Hereditary Osteodystrophy
por: Huso, David L., et al.
Publicado: (2011)

Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction
por: Izzi, Benedetta, et al.
Publicado: (2012)

Bilateral Simultaneous Disc Edema and Cataract Associated with Albright Hereditary Osteodystrophy
por: Sengupta, Sabyasachi, et al.
Publicado: (2012)

Bariatric surgery in an obese patient with Albright hereditary osteodystrophy: a case report
por: Ferrario, Chiara, et al.
Publicado: (2013)

2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance
por: Elli, Francesca Marta, et al.
Publicado: (2019)

A novel variant in the GNAS complex locus causes Albright hereditary osteodystrophy with pseudopseudohypoparathyroidism
por: Smith, Jeffrey S., et al.
Publicado: (2022)

Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation
por: Leclercq, Valérie, et al.
Publicado: (2018)

Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services
por: Noor, Sahar, et al.
Publicado: (2023)

PSAT183 Severe Hypocalcemia Precipitated by COVID-19 Infection in a Patient with Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism
por: Siddiqui, Samrah, et al.
Publicado: (2022)

Ostéodystrophie héréditaire d'Albright: à propos d'une observation
por: Tami, Laila, et al.
Publicado: (2019)

Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?
por: White, M., et al.
Publicado: (2013)

A patient with features of albright hereditory osteodystrophy and unusual neuropsychiatric findings without coding Gsalpha mutations
por: Hasani-Ranjbar, Shirin, et al.
Publicado: (2014)

Hypocalcemic Recurrent Generalized Seizures with Bilateral Basal Ganglia and Frontal Calcification as the Initial Manifestation of Albright’s Hereditary Osteodystrophy in a Child: A Pictorial and Video-graphic Representations
por: Nunavath, Akhilesh Kumar, et al.
Publicado: (2019)

Rickety Osteodystrophy
Publicado: (1935)

Osteodystrophies of jaws
por: Santana, N, et al.
Publicado: (2020)

Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development
por: Krishnan, Neetu, et al.
Publicado: (2023)

Renal osteodystrophy: A historical review of its origins and conceptual evolution
por: Eknoyan, Garabed, et al.
Publicado: (2022)

GS-5734 and its parent nucleoside analog inhibit Filo-, Pneumo-, and Paramyxoviruses
por: Lo, Michael K., et al.
Publicado: (2017)

Osteodystrophy from Cattle Disease
Publicado: (1931)

Parathyreoid Osteodystrophy (Osteitis Fibrosa)
por: Struthers, J. W.
Publicado: (1933)

Post-Traumatic Osteodystrophy at Joints
por: Middleton, D. Stewart, et al.
Publicado: (1934)

Albright's dimpling sign
por: Venkatesh, Chandrasekaran, et al.
Publicado: (2013)

Bone Canopies in Pediatric Renal Osteodystrophy
por: Pereira, Renata C., et al.
Publicado: (2016)

Cyst-like Tumors in Renal Osteodystrophy
por: Li Cavoli, Gioacchino, et al.
Publicado: (2021)

McCune-Albright syndrome
por: Dumitrescu, Claudia E, et al.
Publicado: (2008)

McCune Albright Syndrome
por: Jibbe, Nada, et al.
Publicado: (2020)

Prevalence of Renal Osteodystrophy in African Hemodialysis Patients
por: Bahad, Abdelaali, et al.
Publicado: (2013)

Correction: Bone Canopies in Pediatric Renal Osteodystrophy
por: Pereira, Renata C., et al.
Publicado: (2016)

Gsα deficiency facilitates cardiac remodeling via CREB/ Bmp10-mediated signaling
por: Yin, Ping, et al.
Publicado: (2021)

Divalent ion metabolism and osteodystrophy in chronic renal failure.
por: Kleeman, C. R., et al.
Publicado: (1967)

EXPERIMENTAL FIBROUS OSTEODYSTROPHY (OSTITIS FIBROSA) IN HYPERPARATHYROID DOGS
por: Jaffe, Henry L., et al.
Publicado: (1930)

Opsismodysplasia: Phosphate Wasting Osteodystrophy Responds to Bisphosphonate Therapy
por: Khwaja, Ansab, et al.
Publicado: (2015)

Recent Advances in the Non-invasive Diagnosis of Renal Osteodystrophy
por: Moorthi, Ranjani N, et al.
Publicado: (2013)

Role of the Wnt/β-Catenin Pathway in Renal Osteodystrophy
por: Bisson, Sarah-Kim, et al.
Publicado: (2018)

New Biochemical Serum Markers of Boneturnover in Renal Osteodystrophy
por: Krintus, Magdalena, et al.
Publicado: (2004)

Renal osteodystrophy in the obesity era: Is metabolic syndrome relevant?
por: Da Silva Martins, Janaina, et al.
Publicado: (2017)

Bone Disease in Nephropathic Cystinosis: Beyond Renal Osteodystrophy
por: Machuca-Gayet, Irma, et al.
Publicado: (2020)

Genetic Disorders of Bone or Osteodystrophies of Jaws—A Review
por: Vammi, Sirisha, et al.
Publicado: (2021)

Sclerostin, Osteocytes, and Wnt Signaling in Pediatric Renal Osteodystrophy
por: Laster, Marciana, et al.
Publicado: (2023)

Epidural Hematoma after Minor Trauma on Patient with Biparietal Osteodystrophy
por: Yılmaz, Muhammet Bahadır, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_urq525csi6gnk05mupjpfidcrj