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Lars Bolund

Showing results (41-50 of 184) with videos related to

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Clinical Endocrinology|December 18, 2003
Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Genome Research|September 14, 2012
SOAPindel: efficient identification of indels from short paired readsShengting Li, Ruiqiang Li, Heng Li, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Cancer Biomarkers : Section a of Disease Markers|September 5, 2009
Familial colorectal cancer, can it be identified by microsatellite instability and chromosomal instability? - A case-control studyLone Sunde, Marie Luise Bisgaard, Helle Soll-Johanning, et al.
BMC Biotechnology|September 7, 2010
Sequencing bias: comparison of different protocols of microRNA library constructionGeng Tian, XuYang Yin, Hong Luo, et al.
Cellular Reprogramming|May 24, 2011
DNA methylation in peripheral blood cells of pigs cloned by somatic cell nuclear transferFei Gao, Shengting Li, Lin Lin, et al.
Molecular Genetics and Metabolism|April 23, 2003
Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transferDavid A Holm, Frederik Dagnaes-Hansen, Henrik Simonsen, et al.
Clinical and Experimental Reproductive Medicine|April 16, 2015
The parental origin correlates with the karyotype of human embryos developing from tripronuclear zygotesMette Warming Joergensen, Rodrigo Labouriau, Johnny Hindkjaer, et al.
Plos One|November 13, 2015
Triploidy--Observations in 154 Diandric CasesNanna Brink Scholz, Lars Bolund, Mette Nyegaard, et al.
FEBS Letters|June 6, 2017
Chromatin accessibility and guide sequence secondary structure affect CRISPR-Cas9 gene editing efficiencyKristopher Torp Jensen, Lasse Fløe, Trine Skov Petersen, et al.
Pageof 19

Showing results (41-50 of 184) with videos related to

Sort By:
Pageof 19
Clinical Endocrinology|December 18, 2003
Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Genome Research|September 14, 2012
SOAPindel: efficient identification of indels from short paired readsShengting Li, Ruiqiang Li, Heng Li, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidusJane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Cancer Biomarkers : Section a of Disease Markers|September 5, 2009
Familial colorectal cancer, can it be identified by microsatellite instability and chromosomal instability? - A case-control studyLone Sunde, Marie Luise Bisgaard, Helle Soll-Johanning, et al.
BMC Biotechnology|September 7, 2010
Sequencing bias: comparison of different protocols of microRNA library constructionGeng Tian, XuYang Yin, Hong Luo, et al.
Cellular Reprogramming|May 24, 2011
DNA methylation in peripheral blood cells of pigs cloned by somatic cell nuclear transferFei Gao, Shengting Li, Lin Lin, et al.
Molecular Genetics and Metabolism|April 23, 2003
Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transferDavid A Holm, Frederik Dagnaes-Hansen, Henrik Simonsen, et al.
Clinical and Experimental Reproductive Medicine|April 16, 2015
The parental origin correlates with the karyotype of human embryos developing from tripronuclear zygotesMette Warming Joergensen, Rodrigo Labouriau, Johnny Hindkjaer, et al.
Plos One|November 13, 2015
Triploidy--Observations in 154 Diandric CasesNanna Brink Scholz, Lars Bolund, Mette Nyegaard, et al.
FEBS Letters|June 6, 2017
Chromatin accessibility and guide sequence secondary structure affect CRISPR-Cas9 gene editing efficiencyKristopher Torp Jensen, Lasse Fløe, Trine Skov Petersen, et al.
Pageof 19