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Human genomics

Showing results (681-690 of 1,110) with videos related to

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Human Genomics|December 14, 2011
In-silico human genomics with GeneCardsGil Stelzer, Irina Dalah, Tsippi Iny Stein, et al.
Human Genomics|October 22, 2013
CER1 gene variations associated with bone mineral density, bone markers, and early menopause in postmenopausal womenTheodora Koromila, Panagiotis Georgoulias, Zoe Dailiana, et al.
Human Genomics|July 29, 2015
Epigenetic inheritance and the missing heritabilityMarco Trerotola, Valeria Relli, Pasquale Simeone, et al.
Human Genomics|August 31, 2017
Falling giants and the rise of gene editing: ethics, private interests and the public goodBenjamin Capps, Ruth Chadwick, Yann Joly, et al.
Human Genomics|November 8, 2017
Identification of a novel genetic locus underlying tremor and dystoniaDorota Monies, Hussam Abou Al-Shaar, Ewa A Goljan, et al.
Human Genomics|November 11, 2017
Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancroftiLinda Batsa Debrah, Anna Albers, Alexander Yaw Debrah, et al.
Human Genomics|October 25, 2017
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patientsVasiliki Chondrou, Petros Kolovos, Argyro Sgourou, et al.
Human Genomics|September 6, 2017
Evaluating somatic tumor mutation detection without matched normal samplesJamie K Teer, Yonghong Zhang, Lu Chen, et al.
Human Genomics|November 25, 2020
Microarray analysis identification of key pathways and interaction network of differential gene expressions during osteogenic differentiationFatemeh Khodabandehloo, Sara Taleahmad, Reza Aflatoonian, et al.
Human Genomics|November 10, 2020
Aldh1l2 knockout mouse metabolomics links the loss of the mitochondrial folate enzyme to deregulation of a lipid metabolism observed in rare human disorderNatalia I Krupenko, Jaspreet Sharma, Peter Pediaditakis, et al.
Pageof 111

Showing results (681-690 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|December 14, 2011
In-silico human genomics with GeneCardsGil Stelzer, Irina Dalah, Tsippi Iny Stein, et al.
Human Genomics|October 22, 2013
CER1 gene variations associated with bone mineral density, bone markers, and early menopause in postmenopausal womenTheodora Koromila, Panagiotis Georgoulias, Zoe Dailiana, et al.
Human Genomics|July 29, 2015
Epigenetic inheritance and the missing heritabilityMarco Trerotola, Valeria Relli, Pasquale Simeone, et al.
Human Genomics|August 31, 2017
Falling giants and the rise of gene editing: ethics, private interests and the public goodBenjamin Capps, Ruth Chadwick, Yann Joly, et al.
Human Genomics|November 8, 2017
Identification of a novel genetic locus underlying tremor and dystoniaDorota Monies, Hussam Abou Al-Shaar, Ewa A Goljan, et al.
Human Genomics|November 11, 2017
Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancroftiLinda Batsa Debrah, Anna Albers, Alexander Yaw Debrah, et al.
Human Genomics|October 25, 2017
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patientsVasiliki Chondrou, Petros Kolovos, Argyro Sgourou, et al.
Human Genomics|September 6, 2017
Evaluating somatic tumor mutation detection without matched normal samplesJamie K Teer, Yonghong Zhang, Lu Chen, et al.
Human Genomics|November 25, 2020
Microarray analysis identification of key pathways and interaction network of differential gene expressions during osteogenic differentiationFatemeh Khodabandehloo, Sara Taleahmad, Reza Aflatoonian, et al.
Human Genomics|November 10, 2020
Aldh1l2 knockout mouse metabolomics links the loss of the mitochondrial folate enzyme to deregulation of a lipid metabolism observed in rare human disorderNatalia I Krupenko, Jaspreet Sharma, Peter Pediaditakis, et al.
Pageof 111