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M Carr

Showing results (1231-1240 of 1,288) with videos related to

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American Journal of Human Genetics|December 23, 2023
A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genesErica L Harris, Vincent Roy, Martin Montagne, et al.
Scientific Reports|May 5, 2022
Reversal of diabetic-induced myopathy by swimming exercise in pregnant rats: a translational intervention studyBruna B Catinelli, Patrícia S Rossignoli, Juliana F Floriano, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityKamron Khan, Ahmed Al-Maskari, Martin McKibbin, et al.
British Journal of Cancer|July 13, 2021
Transcriptome profiles of stem-like cells from primary breast cancers allow identification of ITGA7 as a predictive marker of chemotherapy responseNoha Gwili, Stacey J Jones, Waleed Al Amri, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)James A Poulter, Alice E Davidson, Manir Ali, et al.
The Journal of Biological Chemistry|January 29, 2020
The extracellular sulfatase SULF2 promotes liver tumorigenesis by stimulating assembly of a promoter-looping GLI1-STAT3 transcriptional complexRyan M Carr, Paola A Romecin Duran, Ezequiel J Tolosa, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences|April 15, 2021
e-ASPECTS software improves interobserver agreement and accuracy of interpretation of aspects scoreWaleed Brinjikji, Mehdi Abbasi, Catherine Arnold, et al.
Global Change Biology|September 6, 2021
Bright spots as climate-smart marine spatial planning tools for conservation and blue growthAna M Queirós, Elizabeth Talbot, Nicola J Beaumont, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.
Pageof 129

Showing results (1231-1240 of 1,288) with videos related to

Sort By:
Pageof 129
American Journal of Human Genetics|December 23, 2023
A recurrent de novo MAX p.Arg60Gln variant causes a syndromic overgrowth disorder through differential expression of c-Myc target genesErica L Harris, Vincent Roy, Martin Montagne, et al.
Scientific Reports|May 5, 2022
Reversal of diabetic-induced myopathy by swimming exercise in pregnant rats: a translational intervention studyBruna B Catinelli, Patrícia S Rossignoli, Juliana F Floriano, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityKamron Khan, Ahmed Al-Maskari, Martin McKibbin, et al.
British Journal of Cancer|July 13, 2021
Transcriptome profiles of stem-like cells from primary breast cancers allow identification of ITGA7 as a predictive marker of chemotherapy responseNoha Gwili, Stacey J Jones, Waleed Al Amri, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)James A Poulter, Alice E Davidson, Manir Ali, et al.
The Journal of Biological Chemistry|January 29, 2020
The extracellular sulfatase SULF2 promotes liver tumorigenesis by stimulating assembly of a promoter-looping GLI1-STAT3 transcriptional complexRyan M Carr, Paola A Romecin Duran, Ezequiel J Tolosa, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
Interventional Neuroradiology : Journal of Peritherapeutic Neuroradiology, Surgical Procedures and Related Neurosciences|April 15, 2021
e-ASPECTS software improves interobserver agreement and accuracy of interpretation of aspects scoreWaleed Brinjikji, Mehdi Abbasi, Catherine Arnold, et al.
Global Change Biology|September 6, 2021
Bright spots as climate-smart marine spatial planning tools for conservation and blue growthAna M Queirós, Elizabeth Talbot, Nicola J Beaumont, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.
Pageof 129