Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Heidemarie Neitzel

Showing results (31-40 of 54) with videos related to

Pageof 6
Sort By:
Molecular Cytogenetics|February 16, 2018
Evidence for a pre-malignant cell line in a skin biopsy from a patient with Nijmegen breakage syndromeRaneem Habib, Heidemarie Neitzel, Aurelie Ernst, et al.
The Journal of Cell Biology|June 24, 2009
Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1Alexandra Tibelius, Joachim Marhold, Hanswalter Zentgraf, et al.
Blood|June 4, 2011
Fanconi anemia (FA)-associated 3q gains in leukemic transformation consistently target EVI1, but do not affect low TERC expression in FAStefan Meyer, Claire Bristow, Mark Wappett, et al.
Human Mutation|October 8, 2005
The first missense alteration in the MCPH1 gene causes autosomal recessive microcephaly with an extremely mild cellular and clinical phenotypeMarc Trimborn, Reyk Richter, Nadine Sternberg, et al.
Bone|May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.
Aging|June 22, 2020
Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndromeRaneem Habib, Ryong Kim, Heidemarie Neitzel, et al.
Cancer Genetics and Cytogenetics|April 6, 2010
Cytogenetic studies in acute leukemia patients relapsing after allogeneic stem cell transplantationMartin Schmidt-Hieber, Igor W Blau, Gregor Richter, et al.
Plos Pathogens|November 14, 2014
PUL21a-Cyclin A2 interaction is required to protect human cytomegalovirus-infected cells from the deleterious consequences of mitotic entryMartin Eifler, Ralf Uecker, Henry Weisbach, et al.
European Journal of Pediatrics|June 24, 2003
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literatureJörg Seidel, Anita Heller, Gabriele Senger, et al.
American Journal of Human Genetics|June 17, 2004
Mutations in microcephalin cause aberrant regulation of chromosome condensationMarc Trimborn, Sandra M Bell, Clive Felix, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Molecular Cytogenetics|February 16, 2018
Evidence for a pre-malignant cell line in a skin biopsy from a patient with Nijmegen breakage syndromeRaneem Habib, Heidemarie Neitzel, Aurelie Ernst, et al.
The Journal of Cell Biology|June 24, 2009
Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1Alexandra Tibelius, Joachim Marhold, Hanswalter Zentgraf, et al.
Blood|June 4, 2011
Fanconi anemia (FA)-associated 3q gains in leukemic transformation consistently target EVI1, but do not affect low TERC expression in FAStefan Meyer, Claire Bristow, Mark Wappett, et al.
Human Mutation|October 8, 2005
The first missense alteration in the MCPH1 gene causes autosomal recessive microcephaly with an extremely mild cellular and clinical phenotypeMarc Trimborn, Reyk Richter, Nadine Sternberg, et al.
Bone|May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.
Aging|June 22, 2020
Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndromeRaneem Habib, Ryong Kim, Heidemarie Neitzel, et al.
Cancer Genetics and Cytogenetics|April 6, 2010
Cytogenetic studies in acute leukemia patients relapsing after allogeneic stem cell transplantationMartin Schmidt-Hieber, Igor W Blau, Gregor Richter, et al.
Plos Pathogens|November 14, 2014
PUL21a-Cyclin A2 interaction is required to protect human cytomegalovirus-infected cells from the deleterious consequences of mitotic entryMartin Eifler, Ralf Uecker, Henry Weisbach, et al.
European Journal of Pediatrics|June 24, 2003
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literatureJörg Seidel, Anita Heller, Gabriele Senger, et al.
American Journal of Human Genetics|June 17, 2004
Mutations in microcephalin cause aberrant regulation of chromosome condensationMarc Trimborn, Sandra M Bell, Clive Felix, et al.
Pageof 6