Cargando…

Novel insights into congenital surfactant dysfunction disorders by in silico analysis of ABCA3 proteins

Detalles Bibliográficos
Autores principales:	Xiao, Guo-Liang, Gao, Yuan, Hao, Hu, Wei, Tao, Hong, Chun, Wang, Yue, Lin, Ying-Yi, Chi, Xiu-Fang, Liu, Ying, Gao, Hong-Yi, Nie, Chuan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Nature Singapore 2022
Materias:	Research Letter
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974682/ https://www.ncbi.nlm.nih.gov/pubmed/36404394 http://dx.doi.org/10.1007/s12519-022-00645-y

Ejemplares similares

Diagnostic Challenges in Neonatal Respiratory Distress—Congenital Surfactant Metabolism Dysfunction Caused by ABCA3 Mutation
por: Rogulska, Justyna, et al.
Publicado: (2022)

Cryo-EM structures of the human surfactant lipid transporter ABCA3
por: Xie, Tian, et al.
Publicado: (2022)

Structural and Pathogenic Impacts of ABCA4 Variants in Retinal Degenerations—An In-Silico Study
por: Cevik, Senem, et al.
Publicado: (2023)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis
por: Walsh, D. M., et al.
Publicado: (2012)

Novel variants of ABCA4 in Han Chinese families with Stargardt disease
por: Hu, Fang-Yuan, et al.
Publicado: (2020)

Surfactant deficiency syndrome in an infant with a C‐terminal frame shift in ABCA3: A case report
por: Akil, Nour, et al.
Publicado: (2018)

Mitochondrial Dysfunction in Parkinson’s Disease: From Mechanistic Insights to Therapy
por: Gao, Xiao-Yan, et al.
Publicado: (2022)

Surfactant Levels in Congenital Diaphragmatic Hernia
por: Davey, Marcus
Publicado: (2007)

Astrocytic dysfunction induced by ABCA1 deficiency causes optic neuropathy
por: Shinozaki, Youichi, et al.
Publicado: (2022)

Congenital ichthyosiform erythroderma with a novel variant in ABCA12 in a Chinese patient
por: Yang, Zhou, et al.
Publicado: (2020)

Sex-specific lipid dysregulation in the Abca7 knockout mouse brain
por: Fu, YuHong, et al.
Publicado: (2022)

Effects of Deletion of Macrophage ABCA7 on Lipid Metabolism and the Development of Atherosclerosis in the Presence and Absence of ABCA1
por: Meurs, Illiana, et al.
Publicado: (2012)

ABCA13 dysfunction associated with psychiatric disorders causes impaired cholesterol trafficking
por: Nakato, Mitsuhiro, et al.
Publicado: (2020)

A Comprehensive In Silico Analysis of the Functional and Structural Impact of Nonsynonymous SNPs in the ABCA1 Transporter Gene
por: Marín-Martín, Francisco R., et al.
Publicado: (2014)

Surfactant protein C dysfunction with new clinical insights for diffuse alveolar hemorrhage and autoimmunity
por: Tang, Xiaolei, et al.
Publicado: (2019)

Correction: Effects of Deletion of Macrophage ABCA7 on Lipid Metabolism and the Development of Atherosclerosis in the Presence and Absence of ABCA1
por: Meurs, Illiana, et al.
Publicado: (2012)

Congenital Surfactant C Deficiency with Pulmonary Hypertension—A Case Report
por: Chua, Wei Chard, et al.
Publicado: (2022)

In Silico Characterization of the Binding Modes of Surfactants with Bovine Serum Albumin
por: Nnyigide, Osita Sunday, et al.
Publicado: (2019)

Lung surfactant proteins as potential targets of prallethrin: An in silico approach
por: Ghanty, Siddhartha, et al.
Publicado: (2022)

Carriers of Loss-of-Function Mutations in ABCA1 Display Pancreatic β-Cell Dysfunction
por: Vergeer, Menno, et al.
Publicado: (2010)

Moiréless correlations in ABCA graphene
por: Kerelsky, Alexander, et al.
Publicado: (2021)

Drug Allergy and the Risk of Lymph Node Metastasis in Rectal Cancer
por: Gao, Chun, et al.
Publicado: (2014)

Biomedical Advances in ABCA1 Transporter: From Bench to Bedside
por: Choi, Hong Y., et al.
Publicado: (2023)

Identification of Dehydroxytrichostatin A as a Novel Up-Regulator of the ATP-Binding Cassette Transporter A1 (ABCA1)
por: Xu, Yang, et al.
Publicado: (2011)

Genetic and Epigenetic Factors at COL2A1 and ABCA4 Influence Clinical Outcome in Congenital Toxoplasmosis
por: Jamieson, Sarra E., et al.
Publicado: (2008)

In silico analysis of serum miRNA profiles in seronegative and seropositive rheumatoid arthritis patients by small RNA sequencing
por: He, Xiao-Hong, et al.
Publicado: (2023)

Author Correction: In Silico Characterization of the Binding Modes of Surfactants with Bovine Serum Albumin
por: Nnyigide, Osita Sunday, et al.
Publicado: (2020)

Cryo‐EM structures of human ABCA7 provide insights into its phospholipid translocation mechanisms
por: Le, Le Thi My, et al.
Publicado: (2022)

ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants
por: Hu, Fang-Yuan, et al.
Publicado: (2019)

Role of ABCA1 in Cardiovascular Disease
por: Wang, Jing, et al.
Publicado: (2022)

ABCA1 is an extracellular phospholipid translocase
por: Segrest, Jere P., et al.
Publicado: (2022)

Stargardt disease-associated in-frame ABCA4 exon 17 skipping results in significant ABCA4 function
por: Kaltak, Melita, et al.
Publicado: (2023)

The human ortholog of the rodent testis-specific ABC transporter Abca17 is a ubiquitously expressed pseudogene (ABCA17P) and shares a common 5' end with ABCA3
por: Piehler, Armin P, et al.
Publicado: (2006)

Gene Therapy Potential for Genetic Disorders of Surfactant Dysfunction
por: Cooney, Ashley L., et al.
Publicado: (2022)

LRP1 Controls cPLA(2) Phosphorylation, ABCA1 Expression and Cellular Cholesterol Export
por: Zhou, Li, et al.
Publicado: (2009)

Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease
por: Xiang, Qin, et al.
Publicado: (2019)

Association of novel MUC16, MAP3K15 and ABCA1 mutation with giant congenital melanocytic nevus
por: Zhou, Renpeng, et al.
Publicado: (2022)

Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
por: Serra, Gregorio, et al.
Publicado: (2022)

Structural basis of substrate recognition and translocation by human ABCA4
por: Xie, Tian, et al.
Publicado: (2021)

Frequency of ABCA4 mutations in 278 Spanish controls: an insight into the prevalence of autosomal recessive Stargardt disease
por: Riveiro-Alvarez, R, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_b9qghin98hldqa2kc80mrfd816