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MCPH1 is essential for cellular adaptation to the G2‐phase decatenation checkpoint

The FASEB journal, 2019-07, Vol.33 (7), p.8363-8374

2019

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The evolution of metazoan shelterin

Genes & development, 2021-12, Vol.35 (23-24), p.1625-1641

2021

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The E3 ubiquitin ligase APC/CCdh1 degrades MCPH1 after MCPH1‐βTrCP2‐Cdc25A‐mediated mitotic entry to ensure neurogenesis

The EMBO journal, 2017-12, Vol.36 (24), p.3666-3681

2017

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The emerging role of MCPH1/BRIT1 in carcinogenesis

Frontiers in oncology, 2023-01, Vol.13, p.1047588-1047588

2023

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Transgenic rhesus monkeys carrying the human MCPH1 gene copies show human-like neoteny of brain development

National science review, 2019-05, Vol.6 (3), p.480-493

2019

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Functional analysis of a novel intronic variant of MCPH1 with autosomal recessive primary microcephaly

Heliyon, 2024-05, Vol.10 (10), p.e30285, Article e30285

2024

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Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis

EMBO reports, 2024-05, Vol.25 (5), p.2418-2440

2024

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Generation and analysis of mouse embryonic stem cells with knockout of the Mcph1 (microcephalin) gene

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2024-09, Vol.28 (5), p.487-494

2024

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Morphogenesis-coupled DNA repair - in mammalian embryogenesis, morphogenesis and DNA double strand break (DSB) repair are carried out simultaneously to ensure normal development

Journal of radiation research, 2024-05, Vol.65 (3), p.416-419

Noda, Asao

2024

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The analyses of human MCPH1 DNA repair machinery and genetic variations

Open medicine (Warsaw, Poland), 2024-02, Vol.19 (1), p.20240917-20240917

Oluwole, Oluwafemi G.

2024

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MCPH1, beyond its role deciding the brain size

Aging (Albany, NY.), 2021-10, Vol.13 (20), p.23437-23439

2021

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Microcephaly Gene Mcph1 Deficiency Induces p19ARF-Dependent Cell Cycle Arrest and Senescence

International journal of molecular sciences, 2024-05, Vol.25 (9), p.4597

2024

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TALEN-based generation of a cynomolgus monkey disease model for human microcephaly

Cell research, 2016-09, Vol.26 (9), p.1048-1061

2016

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Adaptive evolution of four microcephaly genes and the evolution of brain size in anthropoid primates

Molecular biology and evolution, 2011-01, Vol.28 (1), p.625-638

2011

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Molecular Genetics of Microcephaly Primary Hereditary: An Overview

Brain sciences, 2021-04, Vol.11 (5), p.581

2021

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Investigation of promoter methylation of MCPH1 gene in circulating cell-free DNA of brain tumor patients

Experimental brain research, 2020-09, Vol.238 (9), p.1903-1909

2020

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Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly

International journal of cancer, 2019-10, Vol.145 (8), p.2070-2081

2019

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Hyperammonemic Encephalopathy Associated with Perampanel: Case Report and Discussion

Canadian journal of neurological sciences, 2021-05, Vol.48 (3), p.438-439

2021

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Induced Impairment of Neurogenesis and Brain Diseases

Tang, FengRu

2023

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Prenatal Identification of a Novel Mutation in the MCPH1 Gene Associated with Autosomal Recessive Primary Microcephaly (MCPH) Using Next Generation Sequencing (NGS): A Case Report and Review of the Literature

Children (Basel), 2022-11, Vol.9 (12), p.1879

2022

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Mitotic entry upon Topo II catalytic inhibition is controlled by Chk1 and Plk1

The FEBS journal, 2020-11, Vol.287 (22), p.4933-4951

2020

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DNA damage response in microcephaly development of MCPH1 mouse model

DNA repair, 2013-08, Vol.12 (8), p.645-655

2013

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Expression analysis of the MCPH1/BRIT1 and BRCA1 tumor suppressor genes and telomerase splice variants in epithelial ovarian cancer

Gene, 2018-09, Vol.672, p.34-44

2018

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Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2019-06, Vol.180 (4), p.258-265

2019

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Genetic heterogeneity in Pakistani microcephaly families

Clinical genetics, 2013-05, Vol.83 (5), p.446-451

2013

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MCPH1 is essential for cellular adaptation to the G2‐phase decatenation checkpoint

The evolution of metazoan shelterin

The E3 ubiquitin ligase APC/CCdh1 degrades MCPH1 after MCPH1‐βTrCP2‐Cdc25A‐mediated mitotic entry to ensure neurogenesis

The emerging role of MCPH1/BRIT1 in carcinogenesis

Transgenic rhesus monkeys carrying the human MCPH1 gene copies show human-like neoteny of brain development

Functional analysis of a novel intronic variant of MCPH1 with autosomal recessive primary microcephaly

Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis

Generation and analysis of mouse embryonic stem cells with knockout of the Mcph1 (microcephalin) gene

Morphogenesis-coupled DNA repair - in mammalian embryogenesis, morphogenesis and DNA double strand break (DSB) repair are carried out simultaneously to ensure normal development

The analyses of human MCPH1 DNA repair machinery and genetic variations

MCPH1, beyond its role deciding the brain size

Microcephaly Gene Mcph1 Deficiency Induces p19ARF-Dependent Cell Cycle Arrest and Senescence

TALEN-based generation of a cynomolgus monkey disease model for human microcephaly

Adaptive evolution of four microcephaly genes and the evolution of brain size in anthropoid primates

Molecular Genetics of Microcephaly Primary Hereditary: An Overview

Investigation of promoter methylation of MCPH1 gene in circulating cell-free DNA of brain tumor patients

Tumor suppressor MCPH1 regulates gene expression profiles related to malignant conversion and chromosomal assembly

Hyperammonemic Encephalopathy Associated with Perampanel: Case Report and Discussion

Induced Impairment of Neurogenesis and Brain Diseases

Prenatal Identification of a Novel Mutation in the MCPH1 Gene Associated with Autosomal Recessive Primary Microcephaly (MCPH) Using Next Generation Sequencing (NGS): A Case Report and Review of the Literature

Mitotic entry upon Topo II catalytic inhibition is controlled by Chk1 and Plk1

DNA damage response in microcephaly development of MCPH1 mouse model

Expression analysis of the MCPH1/BRIT1 and BRCA1 tumor suppressor genes and telomerase splice variants in epithelial ovarian cancer

Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia

Genetic heterogeneity in Pakistani microcephaly families

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