Cargando…

Molecular evolutionary analysis of human primary microcephaly genes

BACKGROUND: There has been a rapid increase in the brain size relative to body size during mammalian evolutionary history. In particular, the enlarged and globular brain is the most distinctive anatomical feature of modern humans that set us apart from other extinct and extant primate species. Genet...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pervaiz, Nashaiman, Kang, Hongen, Bao, Yiming, Abbasi, Amir Ali
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8091745/ https://www.ncbi.nlm.nih.gov/pubmed/33941077 http://dx.doi.org/10.1186/s12862-021-01801-0

Ejemplares similares

Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene
por: Seemab, Suman, et al.
Publicado: (2019)

Molecular evolutionary and structural analysis of human UCHL1 gene demonstrates the relevant role of intragenic epistasis in Parkinson’s disease and other neurological disorders
por: Nawaz, Muhammad Saqib, et al.
Publicado: (2020)

Molecular evolution of WDR62, a gene that regulates neocorticogenesis
por: Pervaiz, Nashaiman, et al.
Publicado: (2016)

The Parkinson Disease gene SNCA: Evolutionary and structural insights with pathological implication
por: Siddiqui, Irum Javaid, et al.
Publicado: (2016)

Evolutionary history of the human multigene families reveals widespread gene duplications throughout the history of animals
por: Pervaiz, Nashaiman, et al.
Publicado: (2019)

Evolutionary and structural analysis of SARS-CoV-2 specific evasion of host immunity
por: Hussain, Irfan, et al.
Publicado: (2020)

Molecular genetics of human primary microcephaly: an overview
por: Faheem, Muhammad, et al.
Publicado: (2015)

Time is of the essence: the molecular mechanisms of primary microcephaly
por: Phan, Thao P., et al.
Publicado: (2021)

Molecular Genetics of Microcephaly Primary Hereditary: An Overview
por: Siskos, Nikistratos, et al.
Publicado: (2021)

The molecular landscape of ASPM mutations in primary microcephaly
por: Nicholas, A K, et al.
Publicado: (2009)

Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly
por: Barbelanne, Marine, et al.
Publicado: (2014)

STIL balancing primary microcephaly and cancer
por: Patwardhan, Dhruti, et al.
Publicado: (2018)

Human-Specific Genes, Cortical Progenitor Cells, and Microcephaly
por: Heide, Michael, et al.
Publicado: (2021)

Microcephaly
por: Hanzlik, Emily, et al.
Publicado: (2017)

Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly
por: Kousar, Rizwana, et al.
Publicado: (2011)

A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly
por: Hashmi, Jamil A., et al.
Publicado: (2016)

A Novel Frameshift Mutation in Abnormal Spindle-Like Microcephaly (ASPM) Gene in an Iranian Patient with Primary Microcephaly: A Case Report
por: BAZGIR, Afsaneh, et al.
Publicado: (2019)

Digenic inheritance of human primary microcephaly delineates centrosomal and non‐centrosomal pathways
por: Duerinckx, Sarah, et al.
Publicado: (2019)

Dissecting the Genetic and Etiological Causes of Primary Microcephaly
por: Jean, Francesca, et al.
Publicado: (2020)

tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans
por: Igoillo-Esteve, Mariana, et al.
Publicado: (2013)

Primary microcephaly: do all roads lead to Rome?
por: Thornton, Gemma K., et al.
Publicado: (2009)

Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders
por: Marakhonov, Andrey V., et al.
Publicado: (2018)

Multifaceted Microcephaly-Related Gene MCPH1
por: Kristofova, Martina, et al.
Publicado: (2022)

Genomic Analysis of Korean Patient With Microcephaly
por: Lee, Jiwon, et al.
Publicado: (2021)

The Yin and Yang of Autosomal Recessive Primary Microcephaly Genes: Insights from Neurogenesis and Carcinogenesis
por: Zhou, Xiaokun, et al.
Publicado: (2020)

ANKLE2 ‐related microcephaly: A variable microcephaly syndrome resembling Zika infection
por: Thomas, Ajay X., et al.
Publicado: (2022)

Exploring evolution of brain genes involved in microcephaly through phylogeny and synteny analysis
por: Rauf, Sobiah, et al.
Publicado: (2013)

Human Brain Organoids to Decode Mechanisms of Microcephaly
por: Gabriel, Elke, et al.
Publicado: (2020)

Population surveillance for microcephaly
por: Kirby, Russell S
Publicado: (2016)

Microcephaly in Neurometabolic Diseases
por: Kempińska, Wiktoria, et al.
Publicado: (2022)

Primary microcephaly caused by novel compound heterozygous mutations in ASPM
por: Okamoto, Nobuhiko, et al.
Publicado: (2018)

Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly
por: Boonsawat, Paranchai, et al.
Publicado: (2019)

Autosomal Recessive Primary Microcephaly: Not Just a Small Brain
por: Zaqout, Sami, et al.
Publicado: (2022)

The impact of TP53 activation and apoptosis in primary hereditary microcephaly
por: Iegiani, Giorgia, et al.
Publicado: (2023)

Microcephaly genes evolved adaptively throughout the evolution of eutherian mammals
por: Montgomery, Stephen H, et al.
Publicado: (2014)

A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly
por: AKBARIAZAR, Elinaz, et al.
Publicado: (2013)

Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
por: Naseer, Muhammad I., et al.
Publicado: (2018)

Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly
por: Hassan, Muhammad Jawad, et al.
Publicado: (2007)

Cerebral organoids model human brain development and microcephaly
por: Lancaster, Madeline A., et al.
Publicado: (2013)

Association of Infantile Spasms and Hypsarrhythmia with Primary Microcephaly- Three Case Reports
por: Khanna, Laxmi, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_i0h91nfbiejf1k8nfjbe08ejcu