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Martin Poot

Showing results (61-70 of 100) with videos related to

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Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|June 18, 2002
Insulin-like growth factor binding protein-related protein 1 inhibits proliferation of MCF-7 breast cancer cells via a senescence-like mechanismHeather-Marie P Wilson, Roger S Birnbaum, Martin Poot, et al.
Leukemia Research|August 15, 2009
Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardationSaskia van der Crabben, Ellen van Binsbergen, Margreet Ausems, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|July 11, 2003
Reduced joining of DNA ends correlates with chromosomal instability in three melanoma cell linesThomas M Rünger, Markus Kotas, Martin Poot, et al.
European Journal of Human Genetics : EJHG|July 23, 2009
Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complexMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
European Journal of Medical Genetics|April 23, 2013
Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 casesMartin Poot, Annemarie A Verrijn Stuart, Emma van Daalen, et al.
Aging Cell|February 3, 2007
Functional role of the Werner syndrome RecQ helicase in human fibroblastsKiranjit K Dhillon, Julia Sidorova, Yannick Saintigny, et al.
American Journal of Medical Genetics. Part A|November 24, 2004
Insights from genomic microarrays into structural chromosome rearrangementsJeroen Knijnenburg, Károly Szuhai, Jacques Giltay, et al.
Human Mutation|October 2, 2010
Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletionsFemke Hannes, Jeroen Van Houdt, Oliver W Quarrell, et al.
Neurogenetics|July 8, 2009
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorderMartin Poot, Vera Beyer, Ira Schwaab, et al.
European Journal of Human Genetics : EJHG|October 3, 2008
Wolf-Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regionsHannelie Engbers, Jasper J van der Smagt, Ruben van 't Slot, et al.
Pageof 10

Showing results (61-70 of 100) with videos related to

Sort By:
Pageof 10
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|June 18, 2002
Insulin-like growth factor binding protein-related protein 1 inhibits proliferation of MCF-7 breast cancer cells via a senescence-like mechanismHeather-Marie P Wilson, Roger S Birnbaum, Martin Poot, et al.
Leukemia Research|August 15, 2009
Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardationSaskia van der Crabben, Ellen van Binsbergen, Margreet Ausems, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|July 11, 2003
Reduced joining of DNA ends correlates with chromosomal instability in three melanoma cell linesThomas M Rünger, Markus Kotas, Martin Poot, et al.
European Journal of Human Genetics : EJHG|July 23, 2009
Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complexMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
European Journal of Medical Genetics|April 23, 2013
Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 casesMartin Poot, Annemarie A Verrijn Stuart, Emma van Daalen, et al.
Aging Cell|February 3, 2007
Functional role of the Werner syndrome RecQ helicase in human fibroblastsKiranjit K Dhillon, Julia Sidorova, Yannick Saintigny, et al.
American Journal of Medical Genetics. Part A|November 24, 2004
Insights from genomic microarrays into structural chromosome rearrangementsJeroen Knijnenburg, Károly Szuhai, Jacques Giltay, et al.
Human Mutation|October 2, 2010
Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletionsFemke Hannes, Jeroen Van Houdt, Oliver W Quarrell, et al.
Neurogenetics|July 8, 2009
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorderMartin Poot, Vera Beyer, Ira Schwaab, et al.
European Journal of Human Genetics : EJHG|October 3, 2008
Wolf-Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regionsHannelie Engbers, Jasper J van der Smagt, Ruben van 't Slot, et al.
Pageof 10