نتایج جستجو برای: premature chromosome condensation

تعداد نتایج: 202062  

Journal: :Cancer research 1995
C Badie G Iliakis N Foray G Alsbeih G E Pantellias R Okayasu N Cheong N S Russell A C Begg C F Arlett

A radiation-sensitive fibroblast culture (180BR) established from an acute lymphoblastic leukemia patient who died following radiotherapy is defective in the repair of radiation-induced DNA double-strand breaks. The cells also show a reduced capacity to repair interphase chromosome damage visualized by means of premature chromosome condensation and metaphase chromosome aberrations measured by f...

Journal: :American journal of human genetics 2004
Marc Trimborn Sandra M Bell Clive Felix Yasmin Rashid Hussain Jafri Paul D Griffiths Luitgard M Neumann Alice Krebs André Reis Karl Sperling Heidemarie Neitzel Andrew P Jackson

Microcephalin (MCPH1) is a gene mutated in primary microcephaly, an autosomal recessive neurodevelopmental disorder in which there is a marked reduction in brain size. PCC syndrome is a recently described disorder of microcephaly, short stature, and misregulated chromosome condensation. Here, we report the finding that MCPH1 primary microcephaly and PCC syndrome are allelic disorders, both havi...

2004
S. Hosseini H. Mozdarani Hossein Mozdarani

B iological dosimetry of ionizing radiation is generally performed by scoring dicentrics and/or translocations in chromosome from peripheral blood lymphocytes (pbl) at the first mitosis following in vitro growth stimulation. It is well known that after irradiation, in this procedure mitotic index is low in some individuals, so the scored mitoses might not be representative of the exposed cell p...

2010
Marc Trimborn Mahdi Ghani Diego J. Walther Monika Dopatka Véronique Dutrannoy Andreas Busche Franziska Meyer Stefanie Nowak Jean Nowak Claus Zabel Joachim Klose Veronica Esquitino Masoud Garshasbi Andreas W. Kuss Hans-Hilger Ropers Susanne Mueller Charlotte Poehlmann Ioannis Gavvovidis Detlev Schindler Karl Sperling Heidemarie Neitzel

Mutations in the human gene MCPH1 cause primary microcephaly associated with a unique cellular phenotype with premature chromosome condensation (PCC) in early G2 phase and delayed decondensation post-mitosis (PCC syndrome). The gene encodes the BRCT-domain containing protein microcephalin/BRIT1. Apart from its role in the regulation of chromosome condensation, the protein is involved in the cel...

2011
Sri Ramachandra Maddaly Ravi Deepa Parvathi Govind Pai Sulogna Ghosh Solomon F.D Paul

Premature Chromosome Condensation (PCC) has been shown to be a powerful cytogenetic and cytokinetic tool in understanding cell-cycle analysis(1) and also for diagnostic purposes(2,3). Although PCC is a useful cytogenetic tool, it involves somatic cell hybridizations employing a mitotic partner. Understanding of the factors responsible for chromatin condensation and their mechanism of action can...

2013
Takao Ono Daisuke Yamashita Tatsuya Hirano

Condensins I and II are multisubunit complexes that play essential yet distinct functions in chromosome condensation and segregation in mitosis. Unlike condensin I, condensin II localizes to the nucleus during interphase, but it remains poorly understood what functions condensin II might have before mitotic entry. Here, we report that condensin II changes its chromatin-binding property during S...

Journal: :The Journal of biological chemistry 2011
Justin W Leung Andrea Leitch Jamie L Wood Charles Shaw-Smith Kay Metcalfe Louise S Bicknell Andrew P Jackson Junjie Chen

Primary microcephaly is an autosomal recessive disorder characterized by marked reduction in human brain size. Microcephalin (MCPH1), one of the genes mutated in primary microcephaly, plays an important role in DNA damage checkpoint control and mitotic entry. Additionally, MCPH1 ensures the proper temporal activation of chromosome condensation during mitosis, by acting as a negative regulator o...

Journal: :Oncology reports 2012
Nicolaas A P Franken Suzanne Hovingh Rosemarie Ten Cate Przemek Krawczyk Jan Stap Ron Hoebe Jacob Aten Gerrit W Barendsen

Ionizing radiation-induced foci (IRIF) of DNA repair-related proteins accumulated at DNA double-strand break (DSB) sites have been suggested to be a powerful biodosimetric tool. However, the relationship between IRIF induction and biologically relevant endpoints, such as cell death and formation of chromosome rearrangements is less clear, especial...

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