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Robert Eveleigh

Showing results (1-10 of 18) with videos related to

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Scientific Reports|March 15, 2017
Identification of Elongated Primary Cilia with Impaired Mechanotransduction in Idiopathic Scoliosis PatientsNiaz Oliazadeh, Kristen F Gorman, Robert Eveleigh, et al.
Frontiers in Immunology|January 13, 2018
Accuracy of Programs for the Determination of Human Leukocyte Antigen Alleles from Next-Generation Sequencing DataAntti Larjo, Robert Eveleigh, Elina Kilpeläinen, et al.
Genes and Immunity|October 9, 2019
A point mutation in the linker domain of mouse STAT5A is associated with impaired NK-cell regulationSalma Chehboun, Gabriel André Leiva-Torres, Benoît Charbonneau, et al.
The Pharmacogenomics Journal|February 16, 2022
HLA-B*07:02 and HLA-C*07:02 are associated with trimethoprim-sulfamethoxazole respiratory failureJennifer L Goldman, Jenna O Miller, Neil Miller, et al.
Genes|October 1, 2014
Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and PerspectivesGrégory Caignard, Megan M Eva, Rebekah van Bruggen, et al.
Spine|February 4, 2015
A replication study for association of 53 single nucleotide polymorphisms in ScoliScore test with adolescent idiopathic scoliosis in French-Canadian populationQi Lin Tang, Cedric Julien, Robert Eveleigh, et al.
Journal of Neurosurgery. Pediatrics|March 11, 2023
Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivityTenzin Gayden, Gabriel Crevier-Sorbo, Wajih Jawhar, et al.
The Journal of Pathology|September 27, 2024
Genomic analysis defines distinct pancreatic and neuronal subtypes of lung carcinoidClara Domingo-Sabugo, Saffron Ag Willis-Owen, Amit Mandal, et al.
NPJ Genomic Medicine|February 7, 2024
A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genomeClaude Bhérer, Robert Eveleigh, Katerina Trajanoska, et al.
Journal of Medical Genetics|March 9, 2021
De novo <i>TRPV4</i> Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathyAviel Ragamin, Carolina C Gomes, Karen Bindels-de Heus, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Scientific Reports|March 15, 2017
Identification of Elongated Primary Cilia with Impaired Mechanotransduction in Idiopathic Scoliosis PatientsNiaz Oliazadeh, Kristen F Gorman, Robert Eveleigh, et al.
Frontiers in Immunology|January 13, 2018
Accuracy of Programs for the Determination of Human Leukocyte Antigen Alleles from Next-Generation Sequencing DataAntti Larjo, Robert Eveleigh, Elina Kilpeläinen, et al.
Genes and Immunity|October 9, 2019
A point mutation in the linker domain of mouse STAT5A is associated with impaired NK-cell regulationSalma Chehboun, Gabriel André Leiva-Torres, Benoît Charbonneau, et al.
The Pharmacogenomics Journal|February 16, 2022
HLA-B*07:02 and HLA-C*07:02 are associated with trimethoprim-sulfamethoxazole respiratory failureJennifer L Goldman, Jenna O Miller, Neil Miller, et al.
Genes|October 1, 2014
Mouse ENU Mutagenesis to Understand Immunity to Infection: Methods, Selected Examples, and PerspectivesGrégory Caignard, Megan M Eva, Rebekah van Bruggen, et al.
Spine|February 4, 2015
A replication study for association of 53 single nucleotide polymorphisms in ScoliScore test with adolescent idiopathic scoliosis in French-Canadian populationQi Lin Tang, Cedric Julien, Robert Eveleigh, et al.
Journal of Neurosurgery. Pediatrics|March 11, 2023
Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivityTenzin Gayden, Gabriel Crevier-Sorbo, Wajih Jawhar, et al.
The Journal of Pathology|September 27, 2024
Genomic analysis defines distinct pancreatic and neuronal subtypes of lung carcinoidClara Domingo-Sabugo, Saffron Ag Willis-Owen, Amit Mandal, et al.
NPJ Genomic Medicine|February 7, 2024
A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genomeClaude Bhérer, Robert Eveleigh, Katerina Trajanoska, et al.
Journal of Medical Genetics|March 9, 2021
De novo <i>TRPV4</i> Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathyAviel Ragamin, Carolina C Gomes, Karen Bindels-de Heus, et al.
Pageof 2