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Raquel Blanco

Showing results (51-60 of 56) with videos related to

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Cell Metabolism|December 17, 2013
Partial and transient reduction of glycolysis by PFKFB3 blockade reduces pathological angiogenesisSandra Schoors, Katrien De Bock, Anna Rita Cantelmo, et al.
American Journal of Medical Genetics. Part A|November 27, 2019
International meeting on Wolf-Hirschhorn syndrome: Update on the nosology and new insights on the pathogenic mechanisms for seizures and growth delayJulián Nevado, Karen S Ho, Marcella Zollino, et al.
Cell|August 6, 2013
Role of PFKFB3-driven glycolysis in vessel sproutingKatrien De Bock, Maria Georgiadou, Sandra Schoors, et al.
Frontiers in Genetics|May 2, 2022
Variability in Phelan-McDermid Syndrome in a Cohort of 210 IndividualsJulián Nevado, Sixto García-Miñaúr, María Palomares-Bralo, et al.
Neuromuscular Disorders : NMD|December 13, 2023
Description of clinical and genetic features of 122 patients included in the Spanish Pompe registryRafael Jenaro Martinez-Marin, David Reyes-Leiva, Andrés Nascimento, et al.
Journal of Medical Genetics|November 29, 2022
Clinical description, molecular delineation and genotype-phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patientsElena Martinez-Cayuelas, Fiona Blanco-Kelly, Fermina Lopez-Grondona, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Cell Metabolism|December 17, 2013
Partial and transient reduction of glycolysis by PFKFB3 blockade reduces pathological angiogenesisSandra Schoors, Katrien De Bock, Anna Rita Cantelmo, et al.
American Journal of Medical Genetics. Part A|November 27, 2019
International meeting on Wolf-Hirschhorn syndrome: Update on the nosology and new insights on the pathogenic mechanisms for seizures and growth delayJulián Nevado, Karen S Ho, Marcella Zollino, et al.
Cell|August 6, 2013
Role of PFKFB3-driven glycolysis in vessel sproutingKatrien De Bock, Maria Georgiadou, Sandra Schoors, et al.
Frontiers in Genetics|May 2, 2022
Variability in Phelan-McDermid Syndrome in a Cohort of 210 IndividualsJulián Nevado, Sixto García-Miñaúr, María Palomares-Bralo, et al.
Neuromuscular Disorders : NMD|December 13, 2023
Description of clinical and genetic features of 122 patients included in the Spanish Pompe registryRafael Jenaro Martinez-Marin, David Reyes-Leiva, Andrés Nascimento, et al.
Journal of Medical Genetics|November 29, 2022
Clinical description, molecular delineation and genotype-phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patientsElena Martinez-Cayuelas, Fiona Blanco-Kelly, Fermina Lopez-Grondona, et al.
Pageof 6