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Heidemarie Neitzel

Showing results (21-30 of 54) with videos related to

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Carcinogenesis|July 15, 2006
Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS proteinLars Krüger, Ilja Demuth, Heidemarie Neitzel, et al.
Orphanet Journal of Rare Diseases|January 17, 2007
Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failureBernd Gruhn, Joerg Seidel, Felix Zintl, et al.
Molecular Cytogenetics|July 23, 2025
A homozygous TRIP13 pathogenic variant associated with familiar oocyte arrest and prematurely condensed sperm chromosomesMichal Schweiger, André Reis, Esen Gümüslü, et al.
Cell Cycle (Georgetown, Tex.)|December 15, 2010
MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrestIoannis Gavvovidis, Charlotte Pöhlmann, Juan Alberto Marchal, et al.
American Journal of Human Genetics|February 22, 2002
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive conditionHeidemarie Neitzel, Luitgard M Neumann, Detlev Schindler, et al.
Plos One|September 7, 2012
A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cellsIoannis Gavvovidis, Isabell Rost, Marc Trimborn, et al.
Prenatal Diagnosis|September 2, 2014
Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European populationRolf Becker, Thomas Keller, Rolf-Dieter Wegner, et al.
Nature Cell Biology|June 20, 2006
Regulation of mitotic entry by microcephalin and its overlap with ATR signallingGemma K Alderton, Laura Galbiati, Elen Griffith, et al.
The Journal of Investigative Dermatology|April 17, 2004
Genomic aberrations and survival in cutaneous T cell lymphomasTanja C Fischer, Sylke Gellrich, J Marcus Muche, et al.
Molecular Cytogenetics|March 10, 2010
Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?Anna Polityko, Olga Khurs, Natalia Rumyantseva, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Carcinogenesis|July 15, 2006
Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS proteinLars Krüger, Ilja Demuth, Heidemarie Neitzel, et al.
Orphanet Journal of Rare Diseases|January 17, 2007
Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failureBernd Gruhn, Joerg Seidel, Felix Zintl, et al.
Molecular Cytogenetics|July 23, 2025
A homozygous TRIP13 pathogenic variant associated with familiar oocyte arrest and prematurely condensed sperm chromosomesMichal Schweiger, André Reis, Esen Gümüslü, et al.
Cell Cycle (Georgetown, Tex.)|December 15, 2010
MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrestIoannis Gavvovidis, Charlotte Pöhlmann, Juan Alberto Marchal, et al.
American Journal of Human Genetics|February 22, 2002
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive conditionHeidemarie Neitzel, Luitgard M Neumann, Detlev Schindler, et al.
Plos One|September 7, 2012
A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cellsIoannis Gavvovidis, Isabell Rost, Marc Trimborn, et al.
Prenatal Diagnosis|September 2, 2014
Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European populationRolf Becker, Thomas Keller, Rolf-Dieter Wegner, et al.
Nature Cell Biology|June 20, 2006
Regulation of mitotic entry by microcephalin and its overlap with ATR signallingGemma K Alderton, Laura Galbiati, Elen Griffith, et al.
The Journal of Investigative Dermatology|April 17, 2004
Genomic aberrations and survival in cutaneous T cell lymphomasTanja C Fischer, Sylke Gellrich, J Marcus Muche, et al.
Molecular Cytogenetics|March 10, 2010
Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?Anna Polityko, Olga Khurs, Natalia Rumyantseva, et al.
Pageof 6