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

Pavlos Fanis

Showing results (11-20 of 36) with videos related to

Pageof 4
Sort By:
Hormones (Athens, Greece)|December 27, 2017
GnRH-dependent precocious puberty manifested at the age of 14 months in a girl with 47,XXX karyotypeNicos Skordis, Eleana Ferrari, Aria Antoniadou, et al.
Frontiers in Endocrinology|June 16, 2023
The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genesPavlos Fanis, Nicos Skordis, Meropi Toumba, et al.
Human Mutation|May 23, 2019
A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β-thalassemia majorPavlos Fanis, Ioanna Kousiappa, Marios Phylactides, et al.
Frontiers in Endocrinology|October 23, 2019
Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5'-UTR Region of the Imprinted <i>MKRN3</i> GenePavlos Fanis, Nicos Skordis, Meropi Toumba, et al.
Molecular and Cellular Endocrinology|January 22, 2025
Identification of puberty related miRNAs in the hypothalamus of female micePavlos Fanis, Maria Morrou, Marios Tomazou, et al.
International Journal of Molecular Medicine|November 25, 2021
Molecular modelling of novel ADCY3 variant predicts a molecular target for tackling obesityMeropi Toumba, Pavlos Fanis, Dimitrios Vlachakis, et al.
Hormones (Athens, Greece)|June 27, 2019
46,XY complete gonadal dysgenesis in a familial case with a rare mutation in the desert hedgehog (DHH) geneVassos Neocleous, Pavlos Fanis, Feride Cinarli, et al.
Frontiers in Endocrinology|January 30, 2023
Methylation status of hypothalamic <i>Mkrn3</i> promoter across pubertyPavlos Fanis, Maria Morrou, Marios Tomazou, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 26, 2017
46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek OriginAssimina Galli-Tsinopoulou, Anastasios Serbis, Eleni P Kotanidou, et al.
Journal of Clinical Medicine|January 18, 2020
Proteomic Studies for the Investigation of γ-Globin Induction by Decitabine in Human Primary Erythroid Progenitor CulturesAndria Theodorou, Marios Phylactides, Eleni Katsantoni, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Hormones (Athens, Greece)|December 27, 2017
GnRH-dependent precocious puberty manifested at the age of 14 months in a girl with 47,XXX karyotypeNicos Skordis, Eleana Ferrari, Aria Antoniadou, et al.
Frontiers in Endocrinology|June 16, 2023
The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genesPavlos Fanis, Nicos Skordis, Meropi Toumba, et al.
Human Mutation|May 23, 2019
A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β-thalassemia majorPavlos Fanis, Ioanna Kousiappa, Marios Phylactides, et al.
Frontiers in Endocrinology|October 23, 2019
Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5'-UTR Region of the Imprinted <i>MKRN3</i> GenePavlos Fanis, Nicos Skordis, Meropi Toumba, et al.
Molecular and Cellular Endocrinology|January 22, 2025
Identification of puberty related miRNAs in the hypothalamus of female micePavlos Fanis, Maria Morrou, Marios Tomazou, et al.
International Journal of Molecular Medicine|November 25, 2021
Molecular modelling of novel ADCY3 variant predicts a molecular target for tackling obesityMeropi Toumba, Pavlos Fanis, Dimitrios Vlachakis, et al.
Hormones (Athens, Greece)|June 27, 2019
46,XY complete gonadal dysgenesis in a familial case with a rare mutation in the desert hedgehog (DHH) geneVassos Neocleous, Pavlos Fanis, Feride Cinarli, et al.
Frontiers in Endocrinology|January 30, 2023
Methylation status of hypothalamic <i>Mkrn3</i> promoter across pubertyPavlos Fanis, Maria Morrou, Marios Tomazou, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 26, 2017
46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek OriginAssimina Galli-Tsinopoulou, Anastasios Serbis, Eleni P Kotanidou, et al.
Journal of Clinical Medicine|January 18, 2020
Proteomic Studies for the Investigation of γ-Globin Induction by Decitabine in Human Primary Erythroid Progenitor CulturesAndria Theodorou, Marios Phylactides, Eleni Katsantoni, et al.
Pageof 4