Cargando…

SMAD4 Controls Cancer Cell Metabolism by Regulating Methylmalonic Aciduria Cobalamin Deficiency (cbl) B Type

Suppressor of mothers against decapentaplegic homolog (SMAD) 4 is a pluripotent signaling mediator that regulates myriad cellular functions, including cell growth, cell division, angiogenesis, apoptosis, cell invasion, and metastasis, through transforming growth factor β (TGF-β)-dependent and -indep...

Descripción completa

Detalles Bibliográficos
Autores principales:	Song, Kyoung, Lee, Hun Seok, Jia, Lina, Chelakkot, Chaithanya, Rajasekaran, Nirmal, Shin, Young Kee
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Society for Molecular and Cellular Biology 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200659/ https://www.ncbi.nlm.nih.gov/pubmed/35680374 http://dx.doi.org/10.14348/molcells.2022.0067

Ejemplares similares

Genetic screening in thrombotic microangiopathy: a plea for methylmalonic aciduria with cobalamine C deficiency detection
por: Rafat, Cédric, et al.
Publicado: (2023)

Spectrum and characterization of bi-allelic variants in MMAB causing cblB-type methylmalonic aciduria
por: Forny, Patrick, et al.
Publicado: (2021)

Mouse Models for Methylmalonic Aciduria
por: Peters, Heidi L., et al.
Publicado: (2012)

Renal Involvement in Methylmalonic Aciduria
por: Alkhunaizi, Ahmed M., et al.
Publicado: (2017)

Manic-depressive Psychosis as the Initial Symptom in Adult Siblings with Late-onset Combined Methylmalonic Aciduria and Homocystinemia, Cobalamin C Type
por: Wu, Li-Yong, et al.
Publicado: (2017)

Monitoring Methylmalonic Aciduria by NMR Urinomics
por: Nicolescu, Alina, et al.
Publicado: (2020)

Brain metabolism and neurological symptoms in combined malonic and methylmalonic aciduria
por: Tucci, Sara
Publicado: (2020)

Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria
por: Hu, Shuang, et al.
Publicado: (2018)

An Expanding Spectrum of Complications in Isolated Methylmalonic Aciduria
por: Forny, Patrick, et al.
Publicado: (2020)

Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency
por: Huemer, Martina, et al.
Publicado: (2016)

Resolution of cor pulmonale after medical management in a patient with cblC-type methylmalonic aciduria and homocystinuria: a case report
por: Profitlich, Laurie, et al.
Publicado: (2009)

A critical reappraisal of dietary practices in methylmalonic acidemia raises concerns about the safety of medical foods. Part 2: Cobalamin C deficiency (cblC).()
por: Manoli, Irini, et al.
Publicado: (2015)

Valproate therapy exacerbating intermediate phenotype of methylmalonic aciduria
por: Murgai, Aditya, et al.
Publicado: (2015)

Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation
por: Rosa, Joana, et al.
Publicado: (2018)

Methylmalonic and malonic aciduria in a dog with progressive encephalomyelopathy
por: Podell, Michael, et al.
Publicado: (1996)

Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull’s Eye Maculopathy
por: Collison, Frederick T., et al.
Publicado: (2015)

Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria
por: Marcadier, Julien L, et al.
Publicado: (2013)

The Value of 1H-MRS and MRI in Combined Methylmalonic Aciduria and Homocystinuria
por: Cheng, Ailan, et al.
Publicado: (2019)

Dietary Treatment from Birth to Pregnancy in a Woman with Methylmalonic Aciduria
por: Kowalik, Agnieszka, et al.
Publicado: (2021)

The impact of metabolic stressors on mitochondrial homeostasis in a renal epithelial cell model of methylmalonic aciduria
por: Schumann, Anke, et al.
Publicado: (2023)

Favorable course of previously undiagnosed Methylmalonic Aciduria with Homocystinuria (cblC type) presenting with pulmonary hypertension and aHUS in a young child: a case report
por: De Simone, Luciano, et al.
Publicado: (2018)

Exome sequencing identifies ACSF3 as the cause of Combined Malonic and Methylmalonic Aciduria
por: Sloan, Jennifer L., et al.
Publicado: (2011)

The value of neuroimaging in the assessment and follow-up of early-onset methylmalonic aciduria and homocystinuria()
por: de Benedictis, Fernando M., et al.
Publicado: (2014)

Pulmonary hypertension in late-onset Methylmalonic Aciduria and Homocystinemia: a case report
por: Wen, Ling-yi, et al.
Publicado: (2020)

Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
por: Lucienne, Marie, et al.
Publicado: (2023)

Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type
por: Girisha, Katta Mohan, et al.
Publicado: (2012)

Clinical picture and treatment effects in 5 patients with Methylmalonic aciduria related to MMAA mutations
por: Wesół-Kucharska, Dorota, et al.
Publicado: (2020)

Considerations of expanded carrier screening: Lessons learned from combined malonic and methylmalonic aciduria
por: Gabriel, Marie Cosette, et al.
Publicado: (2021)

Effect of HPV E6/E7 siRNA with Chemotherapeutic Agents on the Regulation of TP53/E2F Dynamic Behavior for Cell Fate Decisions
por: Rajasekaran, Nirmal, et al.
Publicado: (2017)

Methylmalonic acid levels in serum, exosomes, and urine and its association with cblC type methylmalonic acidemia-induced cognitive impairment
por: Sun, Shuqi, et al.
Publicado: (2022)

Early cardiomyopathy without severe metabolic dysregulation in a patient with cblB‐type methylmalonic acidemia
por: Agnarsdóttir, Dagbjört, et al.
Publicado: (2022)

Serum Cobalamin and Methylmalonic Acid Concentrations in Hyperthyroid Cats Before and After Radioiodine Treatment
por: Geesaman, B.M., et al.
Publicado: (2016)

Methylmalonyl Coenzyme A (CoA) Epimerase Deficiency, an Ultra-Rare Cause of Isolated Methylmalonic Aciduria With Predominant Neurological Features
por: Diogo, Rui, et al.
Publicado: (2023)

Combined Malonic and Methylmalonic Aciduria Diagnosed by Recurrent and Severe Infections Mimicking a Primary Immunodeficiency Disease: A Case Report
por: Lee, Joon Kee, et al.
Publicado: (2023)

Case report: Is exchange transfusion a possible treatment for metabolic decompensation in neonates with methylmalonic aciduria in the setting of limited resources?
por: Cui, Xiaoyu, et al.
Publicado: (2022)

Clinical experience with N-carbamylglutamate in a single-centre cohort of patients with propionic and methylmalonic aciduria
por: Burlina, Alberto, et al.
Publicado: (2016)

Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria
por: Grandone, Elvira, et al.
Publicado: (2019)

Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria
por: Schnabel, Elena, et al.
Publicado: (2023)

Very long‐term outcomes in 23 patients with cblA type methylmalonic acidemia
por: Marelli, Cecilia, et al.
Publicado: (2022)

Serum cobalamin and methylmalonic acid concentrations in juvenile dogs with parvoviral enteritis or other acute enteropathies
por: Hung, Michael, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_omt0vlm57me0b3di06a9ku32s7