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B Gardiner

Showing results (51-60 of 61) with videos related to

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Genome Research|November 4, 2010
Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptomeTim R Mercer, Marcel E Dinger, Cameron P Bracken, et al.
Human Molecular Genetics|October 26, 2014
Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defectsAideen M McInerney-Leo, Duncan B Sparrow, Jessica E Harris, et al.
Clinical Genetics|December 11, 2014
Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophiesA M McInerney-Leo, J E Harris, P J Leo, et al.
American Journal of Hematology|April 1, 1983
The occurrence of different levels of G gamma chain and of the A gamma T variant of fetal hemoglobin in newborn babies from several countriesT H Huisman, A L Reese, M B Gardiner, et al.
Genome Research|June 20, 2008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiationMarcel E Dinger, Paulo P Amaral, Tim R Mercer, et al.
BMC Genomics|September 6, 2011
Refining transcriptional programs in kidney development by integration of deep RNA-sequencing and array-based spatial profilingRathi D Thiagarajan, Nicole Cloonan, Brooke B Gardiner, et al.
Genomics|September 7, 2001
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism familiesE L Nurmi, Y Bradford, Y Chen, et al.
American Journal of Medical Genetics|December 3, 1999
An autosomal genomic screen for autism. Collaborative linkage study of autismS Barrett, J C Beck, R Bernier, et al.
Nature|October 30, 2012
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genesAndrew V Biankin, Nicola Waddell, Karin S Kassahn, et al.
Nature|September 15, 2015
Whole-genome sequencing identifies EN1 as a determinant of bone density and fractureHou-Feng Zheng, Vincenzo Forgetta, Yi-Hsiang Hsu, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Genome Research|November 4, 2010
Regulated post-transcriptional RNA cleavage diversifies the eukaryotic transcriptomeTim R Mercer, Marcel E Dinger, Cameron P Bracken, et al.
Human Molecular Genetics|October 26, 2014
Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defectsAideen M McInerney-Leo, Duncan B Sparrow, Jessica E Harris, et al.
Clinical Genetics|December 11, 2014
Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophiesA M McInerney-Leo, J E Harris, P J Leo, et al.
American Journal of Hematology|April 1, 1983
The occurrence of different levels of G gamma chain and of the A gamma T variant of fetal hemoglobin in newborn babies from several countriesT H Huisman, A L Reese, M B Gardiner, et al.
Genome Research|June 20, 2008
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiationMarcel E Dinger, Paulo P Amaral, Tim R Mercer, et al.
BMC Genomics|September 6, 2011
Refining transcriptional programs in kidney development by integration of deep RNA-sequencing and array-based spatial profilingRathi D Thiagarajan, Nicole Cloonan, Brooke B Gardiner, et al.
Genomics|September 7, 2001
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism familiesE L Nurmi, Y Bradford, Y Chen, et al.
American Journal of Medical Genetics|December 3, 1999
An autosomal genomic screen for autism. Collaborative linkage study of autismS Barrett, J C Beck, R Bernier, et al.
Nature|October 30, 2012
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genesAndrew V Biankin, Nicola Waddell, Karin S Kassahn, et al.
Nature|September 15, 2015
Whole-genome sequencing identifies EN1 as a determinant of bone density and fractureHou-Feng Zheng, Vincenzo Forgetta, Yi-Hsiang Hsu, et al.
Pageof 7