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Andrea Messina

Showing results (71-80 of 86) with videos related to

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Elife|July 11, 2019
Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadismSamuel Andrew Malone, Georgios E Papadakis, Andrea Messina, et al.
American Journal of Human Genetics|December 30, 2019
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic HypogonadismAndrea Messina, Kristiina Pulli, Sara Santini, et al.
Human Molecular Genetics|December 5, 2017
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron developmentJustine Bouilly, Andrea Messina, Georgios Papadakis, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2022
Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertilityBalázs Göcz, Éva Rumpler, Miklós Sárvári, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|January 9, 2022
Multimodal evaluation of <sup>19</sup>F-BPA internalization in pancreatic cancer cells for boron capture and proton therapy potential applicationsAndrea Ciardiello, Saverio Altieri, Francesca Ballarini, et al.
Journal of Translational Medicine|January 30, 2025
Multiomics unravels the complexity of male obesity: a prospective observational studyGeorgios E Papadakis, Lucie Favre, Yassine Zouaghi, et al.
European Journal of Human Genetics : EJHG|January 14, 2026
Pleiotropic genes linking congenital hypogonadotropic hypogonadism and cleft lip/palate: evidence from a genomic CHH cohort studyFernanda de Azevedo Correa, Imen Habibi, Jing Zhai, et al.
EMBO Molecular Medicine|July 30, 2017
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
American Journal of Human Genetics|September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Science Translational Medicine|October 5, 2022
<i>NOS1</i> mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceKonstantina Chachlaki, Andrea Messina, Virginia Delli, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Elife|July 11, 2019
Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadismSamuel Andrew Malone, Georgios E Papadakis, Andrea Messina, et al.
American Journal of Human Genetics|December 30, 2019
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic HypogonadismAndrea Messina, Kristiina Pulli, Sara Santini, et al.
Human Molecular Genetics|December 5, 2017
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron developmentJustine Bouilly, Andrea Messina, Georgios Papadakis, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2022
Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertilityBalázs Göcz, Éva Rumpler, Miklós Sárvári, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|January 9, 2022
Multimodal evaluation of <sup>19</sup>F-BPA internalization in pancreatic cancer cells for boron capture and proton therapy potential applicationsAndrea Ciardiello, Saverio Altieri, Francesca Ballarini, et al.
Journal of Translational Medicine|January 30, 2025
Multiomics unravels the complexity of male obesity: a prospective observational studyGeorgios E Papadakis, Lucie Favre, Yassine Zouaghi, et al.
European Journal of Human Genetics : EJHG|January 14, 2026
Pleiotropic genes linking congenital hypogonadotropic hypogonadism and cleft lip/palate: evidence from a genomic CHH cohort studyFernanda de Azevedo Correa, Imen Habibi, Jing Zhai, et al.
EMBO Molecular Medicine|July 30, 2017
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
American Journal of Human Genetics|September 3, 2016
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia DefectsKonstantinos Nikopoulos, Pietro Farinelli, Basilio Giangreco, et al.
Science Translational Medicine|October 5, 2022
<i>NOS1</i> mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceKonstantina Chachlaki, Andrea Messina, Virginia Delli, et al.
Pageof 9