Joost Gribnau

Joost Gribnau

Department of Reproduction and Development, Erasmus MC - University Medical Center

Affiliated withErasmus MC - University Medical Center

Research Area

Biography

Joost Gribnau has not added Biography.
If you are Joost Gribnau and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1
Year
Combined DNA-RNA Fluorescent <em>In situ</em> Hybridization (FISH) to Study X Chromosome Inactivation in Differentiated Female Mouse Embryonic Stem Cells
Publication title

Cited by 14

2014

Other Publications

Article
Year
Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality.

Molecular and cellular biology| PubMed ID: 11884600

2002
2003
2003
2004
2005
2006
X inactivation Xplained.

Current opinion in genetics & development| PubMed ID: 17869504

2007
2008
2008
2008
2009
X chromosome inactivation is initiated in human preimplantation embryos.

American journal of human genetics| PubMed ID: 19481196

2009
2009
X-changing information on X inactivation.

Experimental cell research| PubMed ID: 20083102

2010
2010
2010
2010
X chromosome inactivation and embryonic stem cells.

Advances in experimental medicine and biology| PubMed ID: 21222204

2010
Long Noncoding RNAs and X Chromosome Inactivation.

Progress in molecular and subcellular biology| PubMed ID: 21287133

2011
2011
Xist regulation and function explored.

Human genetics| PubMed ID: 21626138

2011
2011
Precise BAC targeting of genetically polymorphic mouse ES cells.

Nucleic acids research| PubMed ID: 21737430

2011
2012
Origin and evolution of X chromosome inactivation.

Current opinion in cell biology| PubMed ID: 22425180

2012
2012
2012
2012
X chromosome inactivation in the cycle of life.

Development (Cambridge, England)| PubMed ID: 22619385

2012
2013
Different flavors of X-chromosome inactivation in mammals.

Current opinion in cell biology| PubMed ID: 23578369

2013
Structural and numerical changes of chromosome X in patients with esophageal atresia.

European journal of human genetics : EJHG| PubMed ID: 24398799

2014
2014