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Alan J Medlar

Showing results (1-10 of 6) with videos related to

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Nucleic Acids Research|May 16, 2018
AAI-profiler: fast proteome-wide exploratory analysis reveals taxonomic identity, misclassification and contaminationAlan J Medlar, Petri Törönen, Liisa Holm
Pediatric Nephrology (Berlin, Germany)|May 28, 2011
Genetic testing in renal diseaseDetlef Bockenhauer, Alan J Medlar, Emma Ashton, et al.
Annals of Neurology|February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaJoshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Journal of the American Society of Nephrology : JASN|February 23, 2013
Phospholipase A2 receptor (PLA2R1) sequence variants in idiopathic membranous nephropathyMarieke J H Coenen, Julia M Hofstra, Hanna Debiec, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Genome Biology|November 21, 2019
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screensNaihui Zhou, Yuxiang Jiang, Timothy R Bergquist, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nucleic Acids Research|May 16, 2018
AAI-profiler: fast proteome-wide exploratory analysis reveals taxonomic identity, misclassification and contaminationAlan J Medlar, Petri Törönen, Liisa Holm
Pediatric Nephrology (Berlin, Germany)|May 28, 2011
Genetic testing in renal diseaseDetlef Bockenhauer, Alan J Medlar, Emma Ashton, et al.
Annals of Neurology|February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaJoshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Journal of the American Society of Nephrology : JASN|February 23, 2013
Phospholipase A2 receptor (PLA2R1) sequence variants in idiopathic membranous nephropathyMarieke J H Coenen, Julia M Hofstra, Hanna Debiec, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Genome Biology|November 21, 2019
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screensNaihui Zhou, Yuxiang Jiang, Timothy R Bergquist, et al.
Pageof 1