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Natalie D Shaw

Showing results (41-50 of 53) with videos related to

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Environmental Health Perspectives|June 6, 2025
Expanded Tox21 biological assay panel for the prediction of drug-induced liver injury and cardiotoxicityTuan Xu, Masato Ooka, Jinghua Zhao, et al.
Environmental Health Perspectives|July 10, 2026
Expanded Tox21 Biological Assay Panel for the Prediction of Drug-Induced Liver Injury and CardiotoxicityTuan Xu, Masato Ooka, Jinghua Zhao, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2013
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypesFlavia Amanda Costa-Barbosa, Ravikumar Balasubramanian, Kimberly W Keefe, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2020
Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic AmenorrheaAngela Delaney, Adam B Burkholder, Christopher A Lavender, et al.
The Journal of Clinical Endocrinology and Metabolism|July 25, 2015
Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone DeficiencyJin-Ho Choi, Ravikumar Balasubramanian, Phil H Lee, et al.
Neurology|February 5, 2022
Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With <i>SMCHD1</i> VariantsPayam Mohassel, Ning Chang, Kaoru Inoue, et al.
Journal of Pediatric and Adolescent Gynecology|January 15, 2022
The Launch of A Girl's First Period Study: Demystifying Reproductive Hormone Profiles in Adolescent GirlsJanet N Lucien, Madison T Ortega, Madison E Calvert, et al.
Journal of Medical Genetics|June 28, 2019
SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domainRichard J L F Lemmers, Nienke van der Stoep, Patrick J van der Vliet, et al.
Neurology|July 8, 2018
FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutationKarlien Mul, Richard J L F Lemmers, Marjolein Kriek, et al.
Stem Cell Reports|June 11, 2026
Scalable hypothalamic neuron differentiation from human pluripotent stem cells suitable for modeling metabolic disordersVukasin M Jovanovic, Narisu Narisu, Lori L Bonnycastle, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

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Pageof 6
Environmental Health Perspectives|June 6, 2025
Expanded Tox21 biological assay panel for the prediction of drug-induced liver injury and cardiotoxicityTuan Xu, Masato Ooka, Jinghua Zhao, et al.
Environmental Health Perspectives|July 10, 2026
Expanded Tox21 Biological Assay Panel for the Prediction of Drug-Induced Liver Injury and CardiotoxicityTuan Xu, Masato Ooka, Jinghua Zhao, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2013
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypesFlavia Amanda Costa-Barbosa, Ravikumar Balasubramanian, Kimberly W Keefe, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2020
Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic AmenorrheaAngela Delaney, Adam B Burkholder, Christopher A Lavender, et al.
The Journal of Clinical Endocrinology and Metabolism|July 25, 2015
Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone DeficiencyJin-Ho Choi, Ravikumar Balasubramanian, Phil H Lee, et al.
Neurology|February 5, 2022
Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With <i>SMCHD1</i> VariantsPayam Mohassel, Ning Chang, Kaoru Inoue, et al.
Journal of Pediatric and Adolescent Gynecology|January 15, 2022
The Launch of A Girl's First Period Study: Demystifying Reproductive Hormone Profiles in Adolescent GirlsJanet N Lucien, Madison T Ortega, Madison E Calvert, et al.
Journal of Medical Genetics|June 28, 2019
SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domainRichard J L F Lemmers, Nienke van der Stoep, Patrick J van der Vliet, et al.
Neurology|July 8, 2018
FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutationKarlien Mul, Richard J L F Lemmers, Marjolein Kriek, et al.
Stem Cell Reports|June 11, 2026
Scalable hypothalamic neuron differentiation from human pluripotent stem cells suitable for modeling metabolic disordersVukasin M Jovanovic, Narisu Narisu, Lori L Bonnycastle, et al.
Pageof 6