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Showing results (1651-1660 of 2,138) with videos related to
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Microvascular Research
|
June 13, 2020
Bulk and single-cell gene expression analyses reveal aging human choriocapillaris has pro-inflammatory phenotype
Andrew P Voigt, S Scott Whitmore, Kelly Mulfaul, et al.
Molecular Genetics and Metabolism
|
January 12, 2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
Nancy E Braverman, Gerald V Raymond, William B Rizzo, et al.
Ophthalmology
|
September 6, 2001
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier
J E Craig, P N Baird, D L Healey, et al.
Leukemia Research
|
June 19, 2013
Phase I dose escalation study of bortezomib in combination with lenalidomide in patients with myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML)
Eyal C Attar, Philip C Amrein, James W Fraser, et al.
Human Gene Therapy
|
July 13, 2016
Using Patient-Specific Induced Pluripotent Stem Cells and Wild-Type Mice to Develop a Gene Augmentation-Based Strategy to Treat CLN3-Associated Retinal Degeneration
Luke A Wiley, Erin R Burnight, Arlene V Drack, et al.
Leukemia Research
|
June 24, 2011
Outcome of older adults with cytogenetically normal AML (CN-AML) and FLT3 mutations
Harshabad Singh, Salma Asali, Lillian L Werner, et al.
Annals of the Rheumatic Diseases
|
December 7, 2007
Dissemination and evaluation of the ASAS/EULAR recommendations for the management of ankylosing spondylitis: results of a study among 1507 rheumatologists
L Gossec, M Dougados, C Phillips, et al.
Human Mutation
|
June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis
Artur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
Environmental Challenges (Amsterdam, Netherlands)
|
September 19, 2025
First national study on genomic profiling of <i>Escherichia coli</i> in United Arab Emirates (UAE) aquatic environments shows diverse Quinolone and Cephalosporin resistance
A Papadopoulou, C A Moubareck, D Ryder, et al.
Contact Dermatitis
|
September 1, 2005
A multicentre review of the hairdressing allergens tested in the UK
Ruwani P Katugampola, Barry N Statham, John S C English, et al.
Page
of 214
Search research articles
Search
Showing results (1651-1660 of 2,138) with videos related to
Sort By:
Page
of 214
Microvascular Research
|
June 13, 2020
Bulk and single-cell gene expression analyses reveal aging human choriocapillaris has pro-inflammatory phenotype
Andrew P Voigt, S Scott Whitmore, Kelly Mulfaul, et al.
Molecular Genetics and Metabolism
|
January 12, 2016
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines
Nancy E Braverman, Gerald V Raymond, William B Rizzo, et al.
Ophthalmology
|
September 6, 2001
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier
J E Craig, P N Baird, D L Healey, et al.
Leukemia Research
|
June 19, 2013
Phase I dose escalation study of bortezomib in combination with lenalidomide in patients with myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML)
Eyal C Attar, Philip C Amrein, James W Fraser, et al.
Human Gene Therapy
|
July 13, 2016
Using Patient-Specific Induced Pluripotent Stem Cells and Wild-Type Mice to Develop a Gene Augmentation-Based Strategy to Treat CLN3-Associated Retinal Degeneration
Luke A Wiley, Erin R Burnight, Arlene V Drack, et al.
Leukemia Research
|
June 24, 2011
Outcome of older adults with cytogenetically normal AML (CN-AML) and FLT3 mutations
Harshabad Singh, Salma Asali, Lillian L Werner, et al.
Annals of the Rheumatic Diseases
|
December 7, 2007
Dissemination and evaluation of the ASAS/EULAR recommendations for the management of ankylosing spondylitis: results of a study among 1507 rheumatologists
L Gossec, M Dougados, C Phillips, et al.
Human Mutation
|
June 8, 2007
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis
Artur V Cideciyan, Tomas S Aleman, Samuel G Jacobson, et al.
Environmental Challenges (Amsterdam, Netherlands)
|
September 19, 2025
First national study on genomic profiling of <i>Escherichia coli</i> in United Arab Emirates (UAE) aquatic environments shows diverse Quinolone and Cephalosporin resistance
A Papadopoulou, C A Moubareck, D Ryder, et al.
Contact Dermatitis
|
September 1, 2005
A multicentre review of the hairdressing allergens tested in the UK
Ruwani P Katugampola, Barry N Statham, John S C English, et al.
Page
of 214