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Nadine Kraemer

Showing results (1-10 of 22) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|April 16, 2004
bHLH gene expression in the Emx2-deficient dentate gyrus reveals defective granule cells and absence of migrating precursorsJudit Oldekamp, Nadine Kraemer, Gonzalo Alvarez-Bolado, et al.
Neurological Research|June 28, 2012
Reference genes in the developing murine brain and in differentiating embryonic stem cellsNadine Kraemer, Gerda Neubert, Lina Issa, et al.
Cellular and Molecular Life Sciences : CMLS|February 18, 2011
What's the hype about CDK5RAP2?Nadine Kraemer, Lina Issa, Stefanie C R Hauck, et al.
Plos One|September 1, 2015
Novel Alternative Splice Variants of Mouse Cdk5rap2Nadine Kraemer, Lina Issa-Jahns, Gerda Neubert, et al.
The European Journal of Neuroscience|July 6, 2006
Emx2 in the developing hippocampal fissure regionTianyu Zhao, Nadine Kraemer, Judit Oldekamp, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 19, 2012
CDK5RAP2 expression during murine and human brain development correlates with pathology in primary autosomal recessive microcephalyLina Issa, Nadine Kraemer, Christian H Rickert, et al.
Orphanet Journal of Rare Diseases|April 17, 2013
Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutationLina Issa, Katrin Mueller, Katja Seufert, et al.
Cell Cycle (Georgetown, Tex.)|May 6, 2015
Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytesNadine Kraemer, Ethiraj Ravindran, Sami Zaqout, et al.
Cell Cycle (Georgetown, Tex.)|April 3, 2014
Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutationsHao Hu, Vanessa Suckow, Luciana Musante, et al.
Progress in Neurobiology|November 26, 2009
Many roads lead to primary autosomal recessive microcephalyAngela M Kaindl, Sandrine Passemard, Pavan Kumar, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Cerebral Cortex (New York, N.Y. : 1991)|April 16, 2004
bHLH gene expression in the Emx2-deficient dentate gyrus reveals defective granule cells and absence of migrating precursorsJudit Oldekamp, Nadine Kraemer, Gonzalo Alvarez-Bolado, et al.
Neurological Research|June 28, 2012
Reference genes in the developing murine brain and in differentiating embryonic stem cellsNadine Kraemer, Gerda Neubert, Lina Issa, et al.
Cellular and Molecular Life Sciences : CMLS|February 18, 2011
What's the hype about CDK5RAP2?Nadine Kraemer, Lina Issa, Stefanie C R Hauck, et al.
Plos One|September 1, 2015
Novel Alternative Splice Variants of Mouse Cdk5rap2Nadine Kraemer, Lina Issa-Jahns, Gerda Neubert, et al.
The European Journal of Neuroscience|July 6, 2006
Emx2 in the developing hippocampal fissure regionTianyu Zhao, Nadine Kraemer, Judit Oldekamp, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 19, 2012
CDK5RAP2 expression during murine and human brain development correlates with pathology in primary autosomal recessive microcephalyLina Issa, Nadine Kraemer, Christian H Rickert, et al.
Orphanet Journal of Rare Diseases|April 17, 2013
Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutationLina Issa, Katrin Mueller, Katja Seufert, et al.
Cell Cycle (Georgetown, Tex.)|May 6, 2015
Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytesNadine Kraemer, Ethiraj Ravindran, Sami Zaqout, et al.
Cell Cycle (Georgetown, Tex.)|April 3, 2014
Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutationsHao Hu, Vanessa Suckow, Luciana Musante, et al.
Progress in Neurobiology|November 26, 2009
Many roads lead to primary autosomal recessive microcephalyAngela M Kaindl, Sandrine Passemard, Pavan Kumar, et al.
Pageof 3