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

A Tolun

Showing results (11-20 of 50) with videos related to

Pageof 5
Sort By:
Protein Expression and Purification|October 28, 2006
Overexpression and purification of human calcitonin gene-related peptide-receptor component protein in Escherichia coliAdviye A Tolun, Ian M Dickerson, Arun Malhotra
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
DETECTING PORCN MICRODELETIONS IN A LARGE FAMILY WITH FOCAL DERMAL HYPOPLASIAM Seven, A Güven, T M Bozoğlu, et al.
Journal of Paediatrics and Child Health|November 24, 2022
Inborn errors of metabolism refuse to stay-at-home: Experiences of a state-wide biochemical genetics service during the COVID-19 pandemicBea Gutierrez, Ashley Hertzog, Susan Badman, et al.
Cell|October 1, 1976
Two complementary strand-specific termination sites for adenovirus DNA replicationB Weingärtner, E L Winnacker, A Tolun, et al.
The Journal of Biological Chemistry|August 25, 1979
Purification of RNA-DNA hybrids by exclusion chromatographyH Persson, M Perricaudet, A Tolun, et al.
Annals of Human Genetics|January 1, 1996
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and TurksF Calafell, P Underhill, A Tolun, et al.
American Journal of Human Genetics|April 14, 2000
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1G N Kavaslar, S Onengüt, O Derman, et al.
Nucleic Acids Research|June 11, 1991
A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD)J P Hugnot, D Récan, M Jeanpierre, et al.
Journal of Medical Genetics|July 5, 2003
High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasisV N Ninis, M O Kýlýnç, M Kandemir, et al.
Journal of Paediatrics and Child Health|February 15, 2021
Purpuric, delayed child: Beyond septicaemia and into inborn errors of metabolismAshley Hertzog, Arthavan Selvanathan, Adviye A Tolun, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Protein Expression and Purification|October 28, 2006
Overexpression and purification of human calcitonin gene-related peptide-receptor component protein in Escherichia coliAdviye A Tolun, Ian M Dickerson, Arun Malhotra
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
DETECTING PORCN MICRODELETIONS IN A LARGE FAMILY WITH FOCAL DERMAL HYPOPLASIAM Seven, A Güven, T M Bozoğlu, et al.
Journal of Paediatrics and Child Health|November 24, 2022
Inborn errors of metabolism refuse to stay-at-home: Experiences of a state-wide biochemical genetics service during the COVID-19 pandemicBea Gutierrez, Ashley Hertzog, Susan Badman, et al.
Cell|October 1, 1976
Two complementary strand-specific termination sites for adenovirus DNA replicationB Weingärtner, E L Winnacker, A Tolun, et al.
The Journal of Biological Chemistry|August 25, 1979
Purification of RNA-DNA hybrids by exclusion chromatographyH Persson, M Perricaudet, A Tolun, et al.
Annals of Human Genetics|January 1, 1996
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and TurksF Calafell, P Underhill, A Tolun, et al.
American Journal of Human Genetics|April 14, 2000
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1G N Kavaslar, S Onengüt, O Derman, et al.
Nucleic Acids Research|June 11, 1991
A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD)J P Hugnot, D Récan, M Jeanpierre, et al.
Journal of Medical Genetics|July 5, 2003
High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasisV N Ninis, M O Kýlýnç, M Kandemir, et al.
Journal of Paediatrics and Child Health|February 15, 2021
Purpuric, delayed child: Beyond septicaemia and into inborn errors of metabolismAshley Hertzog, Arthavan Selvanathan, Adviye A Tolun, et al.
Pageof 5