The N-terminal BRCT domain determines MCPH1 function in brain development and fertility
Published 2021 View Full Article
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Title
The N-terminal BRCT domain determines MCPH1 function in brain development and fertility
Authors
Keywords
-
Journal
Cell Death & Disease
Volume 12, Issue 2, Pages -
Publisher
Springer Science and Business Media LLC
Online
2021-02-04
DOI
10.1038/s41419-021-03406-3
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Related references
Note: Only part of the references are listed.- The Genetics of Primary Microcephaly
- (2018) Divya Jayaraman et al. Annual Review of Genomics and Human Genetics
- Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
- (2018) Muhammad Naseer et al. Neurosciences
- The DNA damage response molecule MCPH1 in brain development and beyond
- (2016) Xiaoqian Liu et al. ACTA BIOCHIMICA ET BIOPHYSICA SINICA
- Molecular genetics of human primary microcephaly: an overview
- (2015) Muhammad Faheem et al. BMC Medical Genomics
- MCPH1: a window into brain development and evolution
- (2015) Jeremy N. Pulvers Frontiers in Cellular Neuroscience
- Autosomal recessive primary microcephalies (MCPH)
- (2014) Angela M. Kaindl EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
- The overexpression of MCPH1 inhibits cell growth through regulating cell cycle-related proteins and activating cytochrome c-caspase 3 signaling in cervical cancer
- (2014) Li Mai et al. MOLECULAR AND CELLULAR BIOCHEMISTRY
- DNA damage response in microcephaly development of MCPH1 mouse model
- (2013) Zhong-Wei Zhou et al. DNA REPAIR
- Primary Microcephaly Gene MCPH1 Shows Signatures of Tumor Suppressors and Is Regulated by miR-27a in Oral Squamous Cell Carcinoma
- (2013) Thejaswini Venkatesh et al. PLoS One
- Mcph1-Deficient Mice Reveal a Role for MCPH1 in Otitis Media
- (2013) Jing Chen et al. PLoS One
- A Novel MCPH1 Isoform Complements the Defective Chromosome Condensation of Human MCPH1-Deficient Cells
- (2012) Ioannis Gavvovidis et al. PLoS One
- MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1–Cdc25 pathway
- (2011) Ralph Gruber et al. NATURE CELL BIOLOGY
- Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1
- (2010) Muhammad Farooq et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A clinical and molecular genetic study of 112 Iranian families with primary microcephaly
- (2010) H. Darvish et al. JOURNAL OF MEDICAL GENETICS
- Establishment of a Mouse Model with Misregulated Chromosome Condensation due to Defective Mcph1 Function
- (2010) Marc Trimborn et al. PLoS One
- Multiple Roles of BRIT1/MCPH1 in DNA Damage Response, DNA Repair, and Cancer Suppression
- (2010) Shiaw-Yih Lin et al. YONSEI MEDICAL JOURNAL
- BRIT1/MCPH1 Is Essential for Mitotic and Meiotic Recombination DNA Repair and Maintaining Genomic Stability in Mice
- (2010) Yulong Liang et al. PLoS Genetics
- Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1
- (2009) Alexandra Tibelius et al. JOURNAL OF CELL BIOLOGY
- BRIT1/MCPH1 links chromatin remodelling to DNA damage response
- (2009) Guang Peng et al. NATURE CELL BIOLOGY
- Krüppel-like factor 4 is involved in functional differentiation of testicular Sertoli cells
- (2008) Maren Godmann et al. DEVELOPMENTAL BIOLOGY
- MCPH1/BRIT1 cooperates with E2F1 in the activation of checkpoint, DNA repair and apoptosis
- (2008) Shan-Zhong Yang et al. EMBO REPORTS
- Microcephalin/MCPH1 Associates with the Condensin II Complex to Function in Homologous Recombination Repair
- (2008) Jamie L. Wood et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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