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Showing results (701-710 of 716) with videos related to

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Frontiers in Immunology|November 2, 2023
Mucosal immune alterations at the early onset of tissue destruction in chronic obstructive pulmonary diseaseCharlotte de Fays, Vincent Geudens, Iwein Gyselinck, et al.
ERJ Open Research|April 3, 2023
Delineating associations of progressive pleuroparenchymal fibroelastosis in patients with pulmonary fibrosisEyjolfur Gudmundsson, An Zhao, Nesrin Mogulkoc, et al.
Nature Genetics|January 29, 2013
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosisVikram P Sharma, Aimée L Fenwick, Mia S Brockop, et al.
Journal of Medical Genetics|November 26, 2016
Diagnostic value of exome and whole genome sequencing in craniosynostosisKerry A Miller, Stephen R F Twigg, Simon J McGowan, et al.
American Journal of Respiratory and Critical Care Medicine|August 13, 2025
Distinct Morphological Types of Small Airway Obstructions in Smokers with Emphysema and End-Stage COPDVincent Geudens, Charlotte De Fays, Lynn Willems, et al.
American Journal of Human Genetics|March 26, 2019
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental DisorderEduardo Calpena, Alexia Hervieu, Teresa Kaserer, et al.
The European Respiratory Journal|November 16, 2023
Mortality surrogates in combined pulmonary fibrosis and emphysemaAn Zhao, Eyjolfur Gudmundsson, Nesrin Mogulkoc, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|March 30, 2024
Global availability of parenteral nutrition: Pre- and post-COVID-19 pandemic surveysStanislaw Klek, Isabel Martinez Del Rio Requejo, Gil Hardy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2023
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Pageof 72

Showing results (701-710 of 716) with videos related to

Sort By:
Pageof 72
Frontiers in Immunology|November 2, 2023
Mucosal immune alterations at the early onset of tissue destruction in chronic obstructive pulmonary diseaseCharlotte de Fays, Vincent Geudens, Iwein Gyselinck, et al.
ERJ Open Research|April 3, 2023
Delineating associations of progressive pleuroparenchymal fibroelastosis in patients with pulmonary fibrosisEyjolfur Gudmundsson, An Zhao, Nesrin Mogulkoc, et al.
Nature Genetics|January 29, 2013
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosisVikram P Sharma, Aimée L Fenwick, Mia S Brockop, et al.
Journal of Medical Genetics|November 26, 2016
Diagnostic value of exome and whole genome sequencing in craniosynostosisKerry A Miller, Stephen R F Twigg, Simon J McGowan, et al.
American Journal of Respiratory and Critical Care Medicine|August 13, 2025
Distinct Morphological Types of Small Airway Obstructions in Smokers with Emphysema and End-Stage COPDVincent Geudens, Charlotte De Fays, Lynn Willems, et al.
American Journal of Human Genetics|March 26, 2019
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental DisorderEduardo Calpena, Alexia Hervieu, Teresa Kaserer, et al.
The European Respiratory Journal|November 16, 2023
Mortality surrogates in combined pulmonary fibrosis and emphysemaAn Zhao, Eyjolfur Gudmundsson, Nesrin Mogulkoc, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|March 30, 2024
Global availability of parenteral nutrition: Pre- and post-COVID-19 pandemic surveysStanislaw Klek, Isabel Martinez Del Rio Requejo, Gil Hardy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2023
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Pageof 72