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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 insipidus
Jane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Genome Research
|
September 14, 2012
SOAPindel: efficient identification of indels from short paired reads
Shengting 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 insipidus
Jane 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 study
Lone Sunde, Marie Luise Bisgaard, Helle Soll-Johanning, et al.
BMC Biotechnology
|
September 7, 2010
Sequencing bias: comparison of different protocols of microRNA library construction
Geng 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 transfer
Fei 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 transfer
David 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 zygotes
Mette Warming Joergensen, Rodrigo Labouriau, Johnny Hindkjaer, et al.
Plos One
|
November 13, 2015
Triploidy--Observations in 154 Diandric Cases
Nanna 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 efficiency
Kristopher Torp Jensen, Lasse Fløe, Trine Skov Petersen, et al.
Page
of 19
Search research articles
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Showing results (41-50 of 184) with videos related to
Sort By:
Page
of 19
Clinical Endocrinology
|
December 18, 2003
Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus
Jane H Christensen, Charlotte Siggaard, Thomas J Corydon, et al.
Genome Research
|
September 14, 2012
SOAPindel: efficient identification of indels from short paired reads
Shengting 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 insipidus
Jane 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 study
Lone Sunde, Marie Luise Bisgaard, Helle Soll-Johanning, et al.
BMC Biotechnology
|
September 7, 2010
Sequencing bias: comparison of different protocols of microRNA library construction
Geng 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 transfer
Fei 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 transfer
David 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 zygotes
Mette Warming Joergensen, Rodrigo Labouriau, Johnny Hindkjaer, et al.
Plos One
|
November 13, 2015
Triploidy--Observations in 154 Diandric Cases
Nanna 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 efficiency
Kristopher Torp Jensen, Lasse Fløe, Trine Skov Petersen, et al.
Page
of 19