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Beatriz Morte

Showing results (31-40 of 47) with videos related to

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Endocrinology|June 3, 2016
MCT8 Deficiency in Male Mice Mitigates the Phenotypic Abnormalities Associated With the Absence of a Functional Type 3 DeiodinaseJ Patrizia Stohn, M Elena Martinez, Kassey Matoin, et al.
Endocrinology|January 17, 2009
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronineAinhoa Ceballos, Monica M Belinchon, Eduardo Sanchez-Mendoza, et al.
Endocrinology|March 10, 2010
Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter-8- and deiodinase-2-deficient miceBeatriz Morte, Ainhoa Ceballos, Diego Diez, et al.
Endocrinology|May 10, 2008
Thyroid hormone action in the adult brain: gene expression profiling of the effects of single and multiple doses of triiodo-L-thyronine in the rat striatumDiego Diez, Carmen Grijota-Martinez, Patrizia Agretti, et al.
Plos One|May 14, 2014
Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivationBárbara Núñez, Raquel Martínez de Mena, Maria Jesus Obregon, et al.
Cellular Signalling|May 10, 2012
Src kinases catalytic activity regulates proliferation, migration and invasiveness of MDA-MB-231 breast cancer cellsMaría Pilar Sánchez-Bailón, Annarica Calcabrini, Daniel Gómez-Domínguez, et al.
Endocrinology|January 9, 2010
Thyroid hormone regulation of gene expression in the developing rat fetal cerebral cortex: prominent role of the Ca2+/calmodulin-dependent protein kinase IV pathwayBeatriz Morte, Diego Díez, Eva Ausó, et al.
Journal of Human Genetics|February 15, 2024
Expanding the genetic and phenotypic spectrum of congenital myasthenic syndrome: new homozygous VAMP1 splicing variants in 2 novel individualsFrancisco Javier Cotrina-Vinagre, María Elena Rodríguez-García, Lucía Del Pozo-Filíu, et al.
Clinical Genetics|November 14, 2024
AMOTL1 -Associated Multiple Congenital Anomalies (Craniofaciocardiohepatic Syndrome, CFCHS): A Novel Clinical Spectrum Including Craniofacial, Heart and Liver AbnormalitiesNatalia Gallego-Zazo, Jair Tenorio-Castano, Alejandro Parra, et al.
European Journal of Internal Medicine|June 6, 2026
Recurrent t(9;12) translocation disrupting ACVRL1 intron 9 causes hereditary haemorrhagic telangiectasia missed by standard exome sequencing in four unrelated familiesAnna Esteve-Garcia, Irene Madrigal, Cinthia Aguilera, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Endocrinology|June 3, 2016
MCT8 Deficiency in Male Mice Mitigates the Phenotypic Abnormalities Associated With the Absence of a Functional Type 3 DeiodinaseJ Patrizia Stohn, M Elena Martinez, Kassey Matoin, et al.
Endocrinology|January 17, 2009
Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronineAinhoa Ceballos, Monica M Belinchon, Eduardo Sanchez-Mendoza, et al.
Endocrinology|March 10, 2010
Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter-8- and deiodinase-2-deficient miceBeatriz Morte, Ainhoa Ceballos, Diego Diez, et al.
Endocrinology|May 10, 2008
Thyroid hormone action in the adult brain: gene expression profiling of the effects of single and multiple doses of triiodo-L-thyronine in the rat striatumDiego Diez, Carmen Grijota-Martinez, Patrizia Agretti, et al.
Plos One|May 14, 2014
Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivationBárbara Núñez, Raquel Martínez de Mena, Maria Jesus Obregon, et al.
Cellular Signalling|May 10, 2012
Src kinases catalytic activity regulates proliferation, migration and invasiveness of MDA-MB-231 breast cancer cellsMaría Pilar Sánchez-Bailón, Annarica Calcabrini, Daniel Gómez-Domínguez, et al.
Endocrinology|January 9, 2010
Thyroid hormone regulation of gene expression in the developing rat fetal cerebral cortex: prominent role of the Ca2+/calmodulin-dependent protein kinase IV pathwayBeatriz Morte, Diego Díez, Eva Ausó, et al.
Journal of Human Genetics|February 15, 2024
Expanding the genetic and phenotypic spectrum of congenital myasthenic syndrome: new homozygous VAMP1 splicing variants in 2 novel individualsFrancisco Javier Cotrina-Vinagre, María Elena Rodríguez-García, Lucía Del Pozo-Filíu, et al.
Clinical Genetics|November 14, 2024
AMOTL1 -Associated Multiple Congenital Anomalies (Craniofaciocardiohepatic Syndrome, CFCHS): A Novel Clinical Spectrum Including Craniofacial, Heart and Liver AbnormalitiesNatalia Gallego-Zazo, Jair Tenorio-Castano, Alejandro Parra, et al.
European Journal of Internal Medicine|June 6, 2026
Recurrent t(9;12) translocation disrupting ACVRL1 intron 9 causes hereditary haemorrhagic telangiectasia missed by standard exome sequencing in four unrelated familiesAnna Esteve-Garcia, Irene Madrigal, Cinthia Aguilera, et al.
Pageof 5