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M Jablonski

Showing results (151-160 of 186) with videos related to

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Investigative Ophthalmology & Visual Science|November 24, 2006
CTRP5 is a membrane-associated and secretory protein in the RPE and ciliary body and the S163R mutation of CTRP5 impairs its secretionMd Nawajes A Mandal, Vidyullatha Vasireddy, G Bhanuprakash Reddy, et al.
Age (Dordrecht, Netherlands)|April 20, 2013
Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized miceDabney K Johnson, Eugene M Rinchik, Naima Moustaid-Moussa, et al.
Nature|July 20, 2018
Leukaemia hijacks a neural mechanism to invade the central nervous systemHisayuki Yao, Trevor T Price, Gaia Cantelli, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 30, 2013
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndromeM Le Quintrec, J Zuber, B Moulin, et al.
Investigative Ophthalmology & Visual Science|September 28, 2006
Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degenerationVidyullatha Vasireddy, Monica M Jablonski, Md Nawajes A Mandal, et al.
BMJ Open Ophthalmology|April 12, 2025
Genotypes of SNPs of key genes regulate susceptibility and drug sensitivity to neovascular AMD in the human populationJinglin Cui, Hang Lu, Suoxi Wang, et al.
Journal of Clinical Immunology|November 1, 1995
Molecular structure of staphylococcus and streptococcus superantigensP M Schlievert, G A Bohach, D H Ohlendorf, et al.
Bioengineering (Basel, Switzerland)|June 26, 2026
Comparison of Deep Learning Tools for Optic Nerve Axon Quantification Finds Limited Generalizability Upon Independent ValidationBenton Chuter, Noah Emmert, Min Young Kim, et al.
Journal of Medical Genetics|November 25, 2003
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutationA Iannaccone, D K Breuer, X F Wang, et al.
JCI Insight|February 10, 2025
Ablation of Htra1 leads to sub-RPE deposits and photoreceptor abnormalitiesPooja Biswas, DaNae R Woodard, T J Hollingsworth, et al.
Pageof 19

Showing results (151-160 of 186) with videos related to

Sort By:
Pageof 19
Investigative Ophthalmology & Visual Science|November 24, 2006
CTRP5 is a membrane-associated and secretory protein in the RPE and ciliary body and the S163R mutation of CTRP5 impairs its secretionMd Nawajes A Mandal, Vidyullatha Vasireddy, G Bhanuprakash Reddy, et al.
Age (Dordrecht, Netherlands)|April 20, 2013
Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized miceDabney K Johnson, Eugene M Rinchik, Naima Moustaid-Moussa, et al.
Nature|July 20, 2018
Leukaemia hijacks a neural mechanism to invade the central nervous systemHisayuki Yao, Trevor T Price, Gaia Cantelli, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 30, 2013
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndromeM Le Quintrec, J Zuber, B Moulin, et al.
Investigative Ophthalmology & Visual Science|September 28, 2006
Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degenerationVidyullatha Vasireddy, Monica M Jablonski, Md Nawajes A Mandal, et al.
BMJ Open Ophthalmology|April 12, 2025
Genotypes of SNPs of key genes regulate susceptibility and drug sensitivity to neovascular AMD in the human populationJinglin Cui, Hang Lu, Suoxi Wang, et al.
Journal of Clinical Immunology|November 1, 1995
Molecular structure of staphylococcus and streptococcus superantigensP M Schlievert, G A Bohach, D H Ohlendorf, et al.
Bioengineering (Basel, Switzerland)|June 26, 2026
Comparison of Deep Learning Tools for Optic Nerve Axon Quantification Finds Limited Generalizability Upon Independent ValidationBenton Chuter, Noah Emmert, Min Young Kim, et al.
Journal of Medical Genetics|November 25, 2003
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutationA Iannaccone, D K Breuer, X F Wang, et al.
JCI Insight|February 10, 2025
Ablation of Htra1 leads to sub-RPE deposits and photoreceptor abnormalitiesPooja Biswas, DaNae R Woodard, T J Hollingsworth, et al.
Pageof 19