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

Felipe Moreno

Showing results (21-30 of 41) with videos related to

Pageof 5
Sort By:
Archives of Endocrinology and Metabolism|March 13, 2023
Estimated average blood glucose level based on fructosamine levelLuis Jesuino de Oliveira Andrade, Alcina Maria Vinhaes Bittencourt, Luiz Felipe Moreno de Brito, et al.
Cannabis and Cannabinoid Research|May 25, 2021
Therapeutic Prospects of Cannabinoids in the Immunomodulation of Prevalent Autoimmune DiseasesXandy Melissa Rodríguez Mesa, Andrés Felipe Moreno Vergara, Leonardo Andrés Contreras Bolaños, et al.
Revista De La Facultad De Ciencias Medicas (Cordoba, Argentina)|September 16, 2004
[Genetic study of hearing loss in families from Argentina]Raúl A Reynoso, Silvia Hendl, Marìa E Barteik, et al.
Human Pathology|April 17, 2002
Estrogen receptor expression in giant cell tumors of the bonePrimitivo Olivera, Elizabeth Perez, Arturo Ortega, et al.
Plos One|September 17, 2013
A novel splice-site mutation in the GJB2 gene causing mild postlingual hearing impairmentMarta Gandía, Francisco J Del Castillo, Francisco J Rodríguez-Álvarez, et al.
Human Genetics|November 22, 2007
A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expressionAngeles Mencía, Daniel González-Nieto, Silvia Modamio-Høybjør, et al.
Human Molecular Genetics|December 24, 2013
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membraneP Kevin Legan, Richard J Goodyear, Matías Morín, et al.
Nature Genetics|April 14, 2009
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing lossAngeles Mencía, Silvia Modamio-Høybjør, Nick Redshaw, et al.
Human Molecular Genetics|May 30, 2009
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairmentMatías Morín, Keith E Bryan, Fernando Mayo-Merino, et al.
Revista Peruana De Medicina Experimental Y Salud Publica|August 21, 2024
SARS-CoV-2 infection during pregnancy: clinical characteristics and vertical transmission in a referral hospital in PeruClaudia Aracelli Urbina-Alvarez, Julio Cesar Sifuentes-Alvarez, Juan Felipe Moreno-Bocanegra, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Archives of Endocrinology and Metabolism|March 13, 2023
Estimated average blood glucose level based on fructosamine levelLuis Jesuino de Oliveira Andrade, Alcina Maria Vinhaes Bittencourt, Luiz Felipe Moreno de Brito, et al.
Cannabis and Cannabinoid Research|May 25, 2021
Therapeutic Prospects of Cannabinoids in the Immunomodulation of Prevalent Autoimmune DiseasesXandy Melissa Rodríguez Mesa, Andrés Felipe Moreno Vergara, Leonardo Andrés Contreras Bolaños, et al.
Revista De La Facultad De Ciencias Medicas (Cordoba, Argentina)|September 16, 2004
[Genetic study of hearing loss in families from Argentina]Raúl A Reynoso, Silvia Hendl, Marìa E Barteik, et al.
Human Pathology|April 17, 2002
Estrogen receptor expression in giant cell tumors of the bonePrimitivo Olivera, Elizabeth Perez, Arturo Ortega, et al.
Plos One|September 17, 2013
A novel splice-site mutation in the GJB2 gene causing mild postlingual hearing impairmentMarta Gandía, Francisco J Del Castillo, Francisco J Rodríguez-Álvarez, et al.
Human Genetics|November 22, 2007
A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expressionAngeles Mencía, Daniel González-Nieto, Silvia Modamio-Høybjør, et al.
Human Molecular Genetics|December 24, 2013
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membraneP Kevin Legan, Richard J Goodyear, Matías Morín, et al.
Nature Genetics|April 14, 2009
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing lossAngeles Mencía, Silvia Modamio-Høybjør, Nick Redshaw, et al.
Human Molecular Genetics|May 30, 2009
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairmentMatías Morín, Keith E Bryan, Fernando Mayo-Merino, et al.
Revista Peruana De Medicina Experimental Y Salud Publica|August 21, 2024
SARS-CoV-2 infection during pregnancy: clinical characteristics and vertical transmission in a referral hospital in PeruClaudia Aracelli Urbina-Alvarez, Julio Cesar Sifuentes-Alvarez, Juan Felipe Moreno-Bocanegra, et al.
Pageof 5