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Brian Stevenson

Showing results (121-130 of 129) with videos related to

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Clinical and Vaccine Immunology : CVI|December 28, 2007
Borrelia burgdorferi complement regulator-acquiring surface protein 2 (CspZ) as a serological marker of human Lyme diseasePeter Kraiczy, Annekatrin Seling, Catherine A Brissette, et al.
Molecular Microbiology|June 27, 2019
The Lyme disease spirochete's BpuR DNA/RNA-binding protein is differentially expressed during the mammal-tick infectious cycle, which affects translation of the SodA superoxide dismutaseBrandon L Jutras, Christina R Savage, William K Arnold, et al.
American Journal of Medical Genetics. Part A|March 21, 2014
MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr typeLuisa Bonafé, Jinlong Liang, Maria W Gorna, et al.
American Journal of Medical Genetics. Part A|August 20, 2015
NBAS mutations cause a multisystem disorder involving bone, connective tissue, liver, immune system, and retinaNuria Garcia Segarra, Diana Ballhausen, Heather Crawford, et al.
International Journal of Systematic and Evolutionary Microbiology|April 23, 2020
Rejection of the name <i>Borreliella</i> and all proposed species comb. nov. placed thereinGabriele Margos, Santiago Castillo-Ramirez, Sally Cutler, et al.
American Journal of Medical Genetics. Part A|March 27, 2015
Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndromeEsra Dikoglu, Ali Alfaiz, Maria Gorna, et al.
British Dental Journal|November 12, 2022
Oral prehabilitation for patients with head and neck cancer: getting it right - the Restorative Dentistry-UK consensus on a multidisciplinary approach to oral and dental assessment and planning prior to cancer treatmentLorna K McCaul, Stewart Barclay, Peter Nixon, et al.
American Journal of Human Genetics|May 21, 2013
FAM111A mutations result in hypoparathyroidism and impaired skeletal developmentSheila Unger, Maria W Górna, Antony Le Béchec, et al.
EMBO Molecular Medicine|November 19, 2016
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVTHarsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, et al.
Pageof 13

Showing results (121-130 of 129) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 129 results.
Clinical and Vaccine Immunology : CVI|December 28, 2007
Borrelia burgdorferi complement regulator-acquiring surface protein 2 (CspZ) as a serological marker of human Lyme diseasePeter Kraiczy, Annekatrin Seling, Catherine A Brissette, et al.
Molecular Microbiology|June 27, 2019
The Lyme disease spirochete's BpuR DNA/RNA-binding protein is differentially expressed during the mammal-tick infectious cycle, which affects translation of the SodA superoxide dismutaseBrandon L Jutras, Christina R Savage, William K Arnold, et al.
American Journal of Medical Genetics. Part A|March 21, 2014
MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr typeLuisa Bonafé, Jinlong Liang, Maria W Gorna, et al.
American Journal of Medical Genetics. Part A|August 20, 2015
NBAS mutations cause a multisystem disorder involving bone, connective tissue, liver, immune system, and retinaNuria Garcia Segarra, Diana Ballhausen, Heather Crawford, et al.
International Journal of Systematic and Evolutionary Microbiology|April 23, 2020
Rejection of the name <i>Borreliella</i> and all proposed species comb. nov. placed thereinGabriele Margos, Santiago Castillo-Ramirez, Sally Cutler, et al.
American Journal of Medical Genetics. Part A|March 27, 2015
Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndromeEsra Dikoglu, Ali Alfaiz, Maria Gorna, et al.
British Dental Journal|November 12, 2022
Oral prehabilitation for patients with head and neck cancer: getting it right - the Restorative Dentistry-UK consensus on a multidisciplinary approach to oral and dental assessment and planning prior to cancer treatmentLorna K McCaul, Stewart Barclay, Peter Nixon, et al.
American Journal of Human Genetics|May 21, 2013
FAM111A mutations result in hypoparathyroidism and impaired skeletal developmentSheila Unger, Maria W Górna, Antony Le Béchec, et al.
EMBO Molecular Medicine|November 19, 2016
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVTHarsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, et al.
Pageof 13