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E Heath

Showing results (361-370 of 431) with videos related to

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Scientific Reports|April 15, 2025
Permeability scaling relationships of volcanic tuff from core to field scale measurementsDolan D Lucero, S Michelle Bourret, John P Ortiz, et al.
Plos One|October 7, 2016
PG1058 Is a Novel Multidomain Protein Component of the Bacterial Type IX Secretion SystemJacqueline E Heath, Christine A Seers, Paul D Veith, et al.
Clinical Genetics|January 10, 2017
Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasiaJ Barraza-García, C I Rivera-Pedroza, A Hisado-Oliva, et al.
American Journal of Medical Genetics. Part A|December 11, 2020
Delineation of the clinical and radiological features of Stuve-Wiedemann syndrome childhood survivors, four new cases and review of the literatureSofía M Siccha, Anna María Cueto, Manuel Parrón-Pajares, et al.
Blood|June 8, 2022
IL-1β expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC functionSidan Li, Juo-Chin Yao, Karolyn A Oetjen, et al.
European Journal of Medical Genetics|January 31, 2024
ERN BOND: The key European network leveraging diagnosis, research, and treatment for rare bone conditionsLorena Casareto, Natasha M Appelman-Dijkstra, Maria Luisa Brandi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 16, 2015
Heterozygous NPR2 Mutations Cause Disproportionate Short Stature, Similar to Léri-Weill DyschondrosteosisAlfonso Hisado-Oliva, Ana I Garre-Vázquez, Fabiola Santaolalla-Caballero, et al.
International Journal of Systematic Bacteriology|April 1, 1997
Ribotype delineation and description of Staphylococcus sciuri subspecies and their potential as reservoirs of methicillin resistance and staphylolytic enzyme genesW E Kloos, D N Ballard, J A Webster, et al.
American Journal of Medical Genetics. Part A|September 17, 2015
Two novel POC1A mutations in the primordial dwarfism, SOFT syndrome: Clinical homogeneity but also unreported malformationsJimena Barraza-García, Carlos Iván Rivera-Pedroza, Luis Salamanca, et al.
American Journal of Hematology|November 25, 2003
MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivationAmos Toren, Galit Rozenfeld-Granot, Karen E Heath, et al.
Pageof 44

Showing results (361-370 of 431) with videos related to

Sort By:
Pageof 44
Scientific Reports|April 15, 2025
Permeability scaling relationships of volcanic tuff from core to field scale measurementsDolan D Lucero, S Michelle Bourret, John P Ortiz, et al.
Plos One|October 7, 2016
PG1058 Is a Novel Multidomain Protein Component of the Bacterial Type IX Secretion SystemJacqueline E Heath, Christine A Seers, Paul D Veith, et al.
Clinical Genetics|January 10, 2017
Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasiaJ Barraza-García, C I Rivera-Pedroza, A Hisado-Oliva, et al.
American Journal of Medical Genetics. Part A|December 11, 2020
Delineation of the clinical and radiological features of Stuve-Wiedemann syndrome childhood survivors, four new cases and review of the literatureSofía M Siccha, Anna María Cueto, Manuel Parrón-Pajares, et al.
Blood|June 8, 2022
IL-1β expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC functionSidan Li, Juo-Chin Yao, Karolyn A Oetjen, et al.
European Journal of Medical Genetics|January 31, 2024
ERN BOND: The key European network leveraging diagnosis, research, and treatment for rare bone conditionsLorena Casareto, Natasha M Appelman-Dijkstra, Maria Luisa Brandi, et al.
The Journal of Clinical Endocrinology and Metabolism|June 16, 2015
Heterozygous NPR2 Mutations Cause Disproportionate Short Stature, Similar to Léri-Weill DyschondrosteosisAlfonso Hisado-Oliva, Ana I Garre-Vázquez, Fabiola Santaolalla-Caballero, et al.
International Journal of Systematic Bacteriology|April 1, 1997
Ribotype delineation and description of Staphylococcus sciuri subspecies and their potential as reservoirs of methicillin resistance and staphylolytic enzyme genesW E Kloos, D N Ballard, J A Webster, et al.
American Journal of Medical Genetics. Part A|September 17, 2015
Two novel POC1A mutations in the primordial dwarfism, SOFT syndrome: Clinical homogeneity but also unreported malformationsJimena Barraza-García, Carlos Iván Rivera-Pedroza, Luis Salamanca, et al.
American Journal of Hematology|November 25, 2003
MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivationAmos Toren, Galit Rozenfeld-Granot, Karen E Heath, et al.
Pageof 44