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BMC Nephrology
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May 16, 2012
A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy
Bernward Hinkes, Karl F Hilgers, Hanno J Bolz, et al.
Plos One
|
June 17, 2015
Sphingosine-1-Phosphate Is a Novel Regulator of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activity
Firhan A Malik, Anja Meissner, Illya Semenkov, et al.
Clinical & Experimental Ophthalmology
|
April 13, 2019
Genetic testing in patients with retinitis pigmentosa: Features of unsolved cases
Johannes Birtel, Martin Gliem, Akio Oishi, et al.
Bioengineering (Basel, Switzerland)
|
December 30, 2025
Comparative Analysis of Two Measurement Modalities for Ex Vivo Analysis of Corneal Stiffness in Porcine Corneas
Sophia A Reifeltshammer, Hannah Seferovic, Malavika H Nambiar, et al.
Molecular & Cellular Proteomics : MCP
|
December 20, 2023
Interactome Analysis Reveals a Link of the Novel ALMS1-CEP70 Complex to Centrosomal Clusters
Franziska Woerz, Felix Hoffmann, Shibu Antony, et al.
Leukemia & Lymphoma
|
July 27, 2016
Polymerase Chain Reaction Analysis of t(14;18) Junctional Regions in B-Cell Lymphomas
M Kneba, S Eick, S Willigeroth, et al.
Neuroscience
|
August 9, 2011
Phosphodiesterase-5 is a therapeutic target for peripheral neuropathy in diabetic mice
L Wang, M Chopp, A Szalad, et al.
International Journal of Molecular Sciences
|
August 12, 2022
In Vitro Cytotoxicity of D18 and Y6 as Potential Organic Photovoltaic Materials for Retinal Prostheses
Ana Cetkovic, Alessandro Bellapianta, Mihai Irimia-Vladu, et al.
The British Journal of Ophthalmology
|
April 9, 2014
A systematic correlation of morphology and function using spectral domain optical coherence tomography and microperimetry in patients with geographic atrophy
Ramzi G Sayegh, Christopher G Kiss, Christian Simader, et al.
Human Mutation
|
February 16, 2007
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction
Inga Ebermann, Martin Walger, Hendrik P N Scholl, et al.
Page
of 87
Search research articles
Search
Showing results (641-650 of 866) with videos related to
Sort By:
Page
of 87
BMC Nephrology
|
May 16, 2012
A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy
Bernward Hinkes, Karl F Hilgers, Hanno J Bolz, et al.
Plos One
|
June 17, 2015
Sphingosine-1-Phosphate Is a Novel Regulator of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activity
Firhan A Malik, Anja Meissner, Illya Semenkov, et al.
Clinical & Experimental Ophthalmology
|
April 13, 2019
Genetic testing in patients with retinitis pigmentosa: Features of unsolved cases
Johannes Birtel, Martin Gliem, Akio Oishi, et al.
Bioengineering (Basel, Switzerland)
|
December 30, 2025
Comparative Analysis of Two Measurement Modalities for Ex Vivo Analysis of Corneal Stiffness in Porcine Corneas
Sophia A Reifeltshammer, Hannah Seferovic, Malavika H Nambiar, et al.
Molecular & Cellular Proteomics : MCP
|
December 20, 2023
Interactome Analysis Reveals a Link of the Novel ALMS1-CEP70 Complex to Centrosomal Clusters
Franziska Woerz, Felix Hoffmann, Shibu Antony, et al.
Leukemia & Lymphoma
|
July 27, 2016
Polymerase Chain Reaction Analysis of t(14;18) Junctional Regions in B-Cell Lymphomas
M Kneba, S Eick, S Willigeroth, et al.
Neuroscience
|
August 9, 2011
Phosphodiesterase-5 is a therapeutic target for peripheral neuropathy in diabetic mice
L Wang, M Chopp, A Szalad, et al.
International Journal of Molecular Sciences
|
August 12, 2022
In Vitro Cytotoxicity of D18 and Y6 as Potential Organic Photovoltaic Materials for Retinal Prostheses
Ana Cetkovic, Alessandro Bellapianta, Mihai Irimia-Vladu, et al.
The British Journal of Ophthalmology
|
April 9, 2014
A systematic correlation of morphology and function using spectral domain optical coherence tomography and microperimetry in patients with geographic atrophy
Ramzi G Sayegh, Christopher G Kiss, Christian Simader, et al.
Human Mutation
|
February 16, 2007
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction
Inga Ebermann, Martin Walger, Hendrik P N Scholl, et al.
Page
of 87