Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Algirdas Utkus

Showing results (81-90 of 102) with videos related to

Pageof 11
Sort By:
Nutrients|October 16, 2024
Association of Urinary Sodium, Potassium, and the Sodium-to-Potassium Ratio with Impaired Kidney Function Assessed with 24-H Urine AnalysisUrte Zakauskiene, Nomeda Bratcikoviene, Ernesta Macioniene, et al.
Medicina (Kaunas, Lithuania)|September 27, 2025
Evidence for the Pathogenicity of a <i>CFH</i> Variant in a Multigenerational Family with Cuticular DrusenEgle Preiksaitiene, Viktorija Gurskytė, Violeta Mikštienė, et al.
Molecular Genetics & Genomic Medicine|July 21, 2019
Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian familyEvelina Siavrienė, Violeta Mikštienė, Darius Radzevičius, et al.
Pediatric Pulmonology|July 13, 2019
SERPINA1 gene polymorphisms in a population-based ALSPAC cohortDavid S DeLuca, Edita Poluzioroviene, Vaida Taminskiene, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|December 13, 2017
Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndromeDita Pelnena, Birute Burnyte, Eriks Jankevics, et al.
Medicina (Kaunas, Lithuania)|November 11, 2022
PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical CharacterisationEvelina Siavrienė, Živilė Maldžienė, Violeta Mikštienė, et al.
Genes|October 23, 2021
<i>CKM</i> Gene <i>rs8111989</i> Polymorphism and Power Athlete StatusValentina Ginevičienė, Audronė Jakaitienė, Algirdas Utkus, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Two mutations in IFITM5 causing distinct forms of osteogenesis imperfectaEncarna Guillén-Navarro, María Juliana Ballesta-Martínez, María Valencia, et al.
Journal of Psychiatric Research|January 6, 2023
Significantly elevated phosphatidylethanol levels in recent suicide attempters, but not in depressed controls and healthy volunteersRobertas Strumila, Aiste Lengvenyte, Linas Zdanavicius, et al.
Medicina (Kaunas, Lithuania)|March 26, 2022
Donor Splice Site Variant in <i>SLC9A6</i> Causes Christianson Syndrome in a Lithuanian Family: A Case ReportGunda Petraitytė, Violeta Mikštienė, Evelina Siavrienė, et al.
Pageof 11

Showing results (81-90 of 102) with videos related to

Sort By:
Pageof 11
Nutrients|October 16, 2024
Association of Urinary Sodium, Potassium, and the Sodium-to-Potassium Ratio with Impaired Kidney Function Assessed with 24-H Urine AnalysisUrte Zakauskiene, Nomeda Bratcikoviene, Ernesta Macioniene, et al.
Medicina (Kaunas, Lithuania)|September 27, 2025
Evidence for the Pathogenicity of a <i>CFH</i> Variant in a Multigenerational Family with Cuticular DrusenEgle Preiksaitiene, Viktorija Gurskytė, Violeta Mikštienė, et al.
Molecular Genetics & Genomic Medicine|July 21, 2019
Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian familyEvelina Siavrienė, Violeta Mikštienė, Darius Radzevičius, et al.
Pediatric Pulmonology|July 13, 2019
SERPINA1 gene polymorphisms in a population-based ALSPAC cohortDavid S DeLuca, Edita Poluzioroviene, Vaida Taminskiene, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|December 13, 2017
Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndromeDita Pelnena, Birute Burnyte, Eriks Jankevics, et al.
Medicina (Kaunas, Lithuania)|November 11, 2022
PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical CharacterisationEvelina Siavrienė, Živilė Maldžienė, Violeta Mikštienė, et al.
Genes|October 23, 2021
<i>CKM</i> Gene <i>rs8111989</i> Polymorphism and Power Athlete StatusValentina Ginevičienė, Audronė Jakaitienė, Algirdas Utkus, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Two mutations in IFITM5 causing distinct forms of osteogenesis imperfectaEncarna Guillén-Navarro, María Juliana Ballesta-Martínez, María Valencia, et al.
Journal of Psychiatric Research|January 6, 2023
Significantly elevated phosphatidylethanol levels in recent suicide attempters, but not in depressed controls and healthy volunteersRobertas Strumila, Aiste Lengvenyte, Linas Zdanavicius, et al.
Medicina (Kaunas, Lithuania)|March 26, 2022
Donor Splice Site Variant in <i>SLC9A6</i> Causes Christianson Syndrome in a Lithuanian Family: A Case ReportGunda Petraitytė, Violeta Mikštienė, Evelina Siavrienė, et al.
Pageof 11