Cargando…

rhIGF-1 Therapy for Growth Failure and IGF-1 Deficiency in Congenital Disorder of Glycosylation Ia (PMM2 Deficiency)

Background. Congenital disorders of glycosylation (CDG) are a group of rare disorders in which glycosylation required for proper protein-protein interactions and protein stability is disrupted, manifesting clinically with multiple system involvement and growth failure. The insulin-like growth factor...

Descripción completa

Detalles Bibliográficos
Autores principales:	Miller, Bradley S., Duffy, Meghann M., Addo, O. Yaw, Sarafoglou, Kyriakie
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2013
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586814/ https://www.ncbi.nlm.nih.gov/pubmed/26425584 http://dx.doi.org/10.1177/2324709613503316

Ejemplares similares

Assessment of compatibility of rhIGF-1/rhIGFBP-3 with neonatal intravenous medications
por: Salamat-Miller, Nazila, et al.
Publicado: (2022)

rhIGF-1 Therapy: A Silver Bullet for Bronchopulmonary Dysplasia Prevention?
por: Plosa, Erin J., et al.
Publicado: (2020)

Effectiveness and safety of rhIGF1 therapy in patients with or without Laron syndrome
por: Bang, Peter, et al.
Publicado: (2020)

rhIGF-1/rhIGFBP-3 in Preterm Infants: A Phase 2 Randomized Controlled Trial
por: Ley, David, et al.
Publicado: (2018)

rhIGF-1/BP3 Preserves Lung Growth and Prevents Pulmonary Hypertension in Experimental Bronchopulmonary Dysplasia
por: Seedorf, Gregory, et al.
Publicado: (2020)

Expression of Recombinant Human Insulin-like Growth Factor Type 1 (rhIGF-1) in Escherichia coli
por: Iranpoor, Hamidreza, et al.
Publicado: (2015)

Pilot dose-ranging of rhIGF-1/rhIGFBP-3 in a preterm lamb model of evolving bronchopulmonary dysplasia
por: Albertine, Kurt H., et al.
Publicado: (2023)

The role of rhIGF-1/BP3 in the prevention of pulmonary hypertension in bronchopulmonary dysplasia and its underlying mechanism
por: Qu, Sehua, et al.
Publicado: (2023)

Subcutaneous administration of rhIGF-I post irradiation exposure enhances hematopoietic recovery and survival in BALB/c mice
por: Chen, Shilei, et al.
Publicado: (2012)

Randomized Control Trial of Postnatal rhIGF-1/rhIGFBP-3 Replacement in Preterm Infants: Post-hoc Analysis of Its Effect on Brain Injury
por: Horsch, Sandra, et al.
Publicado: (2020)

Defective IGF-1 prohormone N-glycosylation and reduced IGF-1 receptor signaling activation in congenital disorders of glycosylation
por: Di Patria, Laura, et al.
Publicado: (2022)

SUN-251 Tanner Stage Adjustment of CDC Height Curves and Potential Clinical Applications
por: Addo, O. Yaw, et al.
Publicado: (2019)

Development of Tanner Stage–Age Adjusted CDC Height Curves for Research and Clinical Applications
por: Miller, Bradley S, et al.
Publicado: (2020)

PMM2‐CDG caused by uniparental disomy: Case report and literature review
por: Vaes, Laurien, et al.
Publicado: (2020)

Sexual dimorphic effects of igf1 deficiency on metabolism in zebrafish
por: Zeng, Ningmei, et al.
Publicado: (2022)

Serum IGF1 and linear growth in children with congenital leptin deficiency before and after leptin substitution
por: Beghini, Marianna, et al.
Publicado: (2021)

Average IGF-1 Prediction for Once-Weekly Lonapegsomatropin in Children With Growth Hormone Deficiency
por: Lin, Zhengning, et al.
Publicado: (2021)

Non-glycosylated IGF2 prohormones are more mitogenic than native IGF2
por: Potalitsyn, Pavlo, et al.
Publicado: (2023)

Autophagy resolves early retinal inflammation in Igf1-deficient mice
por: Arroba, Ana I., et al.
Publicado: (2016)

Role of IGF-1R in ameliorating apoptosis of GNE deficient cells
por: Singh, Reema, et al.
Publicado: (2018)

IGF1 deficiency integrates stunted growth and neurodegeneration in Down syndrome
por: Araya, Paula, et al.
Publicado: (2022)

Baseline IGFBP - 3 as the Key Element to Predict Growth Response to Growth Hormone and IGF - 1 Therapy in Subjects with Non - GH Deficient Short Stature and IGF - 1 Deficiency
por: Perez-Colon, Sheila, et al.
Publicado: (2018)

Evaluation of Cell Models to Study Monocyte Functions in PMM2 Congenital Disorders of Glycosylation
por: de Haas, Paola, et al.
Publicado: (2022)

IGF2: The Achilles' heel of p53-deficiency?
por: Clermont, Frederic, et al.
Publicado: (2012)

Experimental approach to IGF-1 therapy in CCl(4)-induced acute liver damage in healthy controls and mice with partial IGF-1 deficiency
por: Morales-Garza, Luis A., et al.
Publicado: (2017)

IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
por: Toth, Peter, et al.
Publicado: (2015)

Clinical and molecular diagnosis of a cartilage‐hair hypoplasia with IGF‐1 deficiency
por: Castilla‐Cortázar, Inma, et al.
Publicado: (2016)

IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal
por: Ibba, Anastasia, et al.
Publicado: (2020)

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2
por: Chan, Barden, et al.
Publicado: (2016)

Anesthetic management of a child with phosphomannomutase-2 congenital disorder of glycosylation (PMM2-CDG)
por: Sakai, Wataru, et al.
Publicado: (2017)

IGF2 deficiency causes mitochondrial defects in skeletal muscle
por: Zhu, Yiyi, et al.
Publicado: (2021)

Macular Hypoplasia in Congenital Disorder of Glycosylation Type Ia
por: Wang, Bob Z., et al.
Publicado: (2012)

Disparate Central and Peripheral Effects of Circulating IGF-1 Deficiency on Tissue Mitochondrial Function
por: Pharaoh, Gavin, et al.
Publicado: (2019)

Circulating LEAP-2 Levels in Adult Growth Hormone Deficiency and Their Relationship With IGF-1
por: Vergani, Edoardo, et al.
Publicado: (2021)

Phosphomannomutase deficiency (PMM2-CDG): ataxia and cerebellar assessment
por: Serrano, Mercedes, et al.
Publicado: (2015)

Sex non-specific growth charts and potential clinical implications in the care of transgender youth
por: Bomberg, Eric Morris, et al.
Publicado: (2023)

A zebrafish model of PMM2-CDG reveals altered neurogenesis and a substrate-accumulation mechanism for N-linked glycosylation deficiency
por: Cline, Abigail, et al.
Publicado: (2012)

IGF1R Deficiency Modulates Brain Signaling Pathways and Disturbs Mitochondria and Redox Homeostasis
por: Cardoso, Susana, et al.
Publicado: (2021)

Cartilage-specific Sirt6 deficiency represses IGF-1 and enhances osteoarthritis severity in mice
por: Collins, John A, et al.
Publicado: (2023)

Delayed skeletal development and IGF-1 deficiency in a mouse model of lysinuric protein intolerance
por: Stroup, Bridget M., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_ns0314nac09mgp6srktsfrotvm