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L Welch

Showing results (451-460 of 476) with videos related to

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American Journal of Respiratory and Critical Care Medicine|November 11, 2022
Molecular Function and Contribution of <i>TBX4</i> in Development and DiseaseJustyna A Karolak, Carrie L Welch, Christian Mosimann, et al.
Nature Communications|December 9, 2025
Multiplexed detection of febrile infections using CARMENM Kamariza, K McMahon, L Kim, et al.
Journal of Medical Genetics|January 30, 2026
Expanding the phenotypic spectrum of <i>MECOM</i>-associated syndrome: rare variants are associated with syndromic pulmonary arterial hypertensionCarrie L Welch, Meriel McEntagart, Shahin Moledina, et al.
Circulation|March 21, 2020
Novel Mutations and Decreased Expression of the Epigenetic Regulator <i>TET2</i> in Pulmonary Arterial HypertensionFrançois Potus, Michael W Pauciulo, Elina K Cook, et al.
Circulation. Genomic and Precision Medicine|April 11, 2018
Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With AdultsNa Zhu, Claudia Gonzaga-Jauregui, Carrie L Welch, et al.
Leukemia|October 6, 2019
Early hospital discharge after intensive induction chemotherapy for adults with acute myeloid leukemia or other high-grade myeloid neoplasmAnna B Halpern, Nicholas P Howard, Megan Othus, et al.
Journal of Medical Genetics|September 8, 2021
Biallelic variants of <i>ATP13A3</i> cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortalityRajiv D Machado, Carrie L Welch, Matthias Haimel, et al.
Genome Medicine|July 22, 2018
Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart diseaseNa Zhu, Carrie L Welch, Jiayao Wang, et al.
Medrxiv : the Preprint Server for Health Sciences|November 9, 2021
Equipment-free detection of SARS-CoV-2 and Variants of Concern using Cas13Jon Arizti-Sanz, A'Doriann Bradley, Yibin B Zhang, et al.
Genome Medicine|June 23, 2021
Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAHNa Zhu, Emilia M Swietlik, Carrie L Welch, et al.
Pageof 48

Showing results (451-460 of 476) with videos related to

Sort By:
Pageof 48
American Journal of Respiratory and Critical Care Medicine|November 11, 2022
Molecular Function and Contribution of <i>TBX4</i> in Development and DiseaseJustyna A Karolak, Carrie L Welch, Christian Mosimann, et al.
Nature Communications|December 9, 2025
Multiplexed detection of febrile infections using CARMENM Kamariza, K McMahon, L Kim, et al.
Journal of Medical Genetics|January 30, 2026
Expanding the phenotypic spectrum of <i>MECOM</i>-associated syndrome: rare variants are associated with syndromic pulmonary arterial hypertensionCarrie L Welch, Meriel McEntagart, Shahin Moledina, et al.
Circulation|March 21, 2020
Novel Mutations and Decreased Expression of the Epigenetic Regulator <i>TET2</i> in Pulmonary Arterial HypertensionFrançois Potus, Michael W Pauciulo, Elina K Cook, et al.
Circulation. Genomic and Precision Medicine|April 11, 2018
Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With AdultsNa Zhu, Claudia Gonzaga-Jauregui, Carrie L Welch, et al.
Leukemia|October 6, 2019
Early hospital discharge after intensive induction chemotherapy for adults with acute myeloid leukemia or other high-grade myeloid neoplasmAnna B Halpern, Nicholas P Howard, Megan Othus, et al.
Journal of Medical Genetics|September 8, 2021
Biallelic variants of <i>ATP13A3</i> cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortalityRajiv D Machado, Carrie L Welch, Matthias Haimel, et al.
Genome Medicine|July 22, 2018
Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart diseaseNa Zhu, Carrie L Welch, Jiayao Wang, et al.
Medrxiv : the Preprint Server for Health Sciences|November 9, 2021
Equipment-free detection of SARS-CoV-2 and Variants of Concern using Cas13Jon Arizti-Sanz, A'Doriann Bradley, Yibin B Zhang, et al.
Genome Medicine|June 23, 2021
Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAHNa Zhu, Emilia M Swietlik, Carrie L Welch, et al.
Pageof 48