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Cold Spring Harbor molecular case studies

Showing results (11-20 of 479) with videos related to

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Cold Spring Harbor Molecular Case Studies|May 6, 2016
Salivary FOXP2 expression and oral feeding success in premature infantsEmily Zimmerman, Monika Maki, Jill Maron
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Molecular analysis of a male breast cancer patient with prolonged stable disease under mTOR/PI3K inhibitors BEZ235/everolimusA Rose Brannon, Melissa Frizziero, David Chen, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Putative BRAF activating fusion in a medullary thyroid cancerKatayoon Kasaian, Sam M Wiseman, Blair A Walker, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Somatic overgrowth associated with homozygous mutations in both MAN1B1 and SEC23ASwati Gupta, Somayyeh Fahiminiya, Tracy Wang, et al.
Cold Spring Harbor Molecular Case Studies|March 10, 2019
De novo missense variant in the GTPase effector domain (GED) of <i>DNM1L</i> leads to static encephalopathy and seizuresNurit Assia Batzir, Pranjali K Bhagwat, Tanya N Eble, et al.
Cold Spring Harbor Molecular Case Studies|November 18, 2018
A newly identified mutation in the <i>PEX26</i> gene is associated with a milder form of Zellweger spectrum disorderAkemi J Tanaka, Kanji Okumoto, Shigehiko Tamura, et al.
Cold Spring Harbor Molecular Case Studies|February 17, 2021
The gut microbiome: a missing link in understanding the gastrointestinal manifestations of COVID-19?Erin F Brooks, Ami S Bhatt
Cold Spring Harbor Molecular Case Studies|February 11, 2021
A novel variant of <i>CDK19</i> causes a severe neurodevelopmental disorder with infantile spasmsShenghai Yang, Weishi Yu, Qian Chen, et al.
Cold Spring Harbor Molecular Case Studies|March 17, 2017
<i>AIFM1</i> mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infantSarah U Morton, Sanjay P Prabhu, Hart G W Lidov, et al.
Cold Spring Harbor Molecular Case Studies|October 19, 2017
Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1CMari Auranen, Jussi Toppila, Saranya Suriyanarayanan, et al.
Pageof 48

Showing results (11-20 of 479) with videos related to

Sort By:
Pageof 48
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Salivary FOXP2 expression and oral feeding success in premature infantsEmily Zimmerman, Monika Maki, Jill Maron
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Molecular analysis of a male breast cancer patient with prolonged stable disease under mTOR/PI3K inhibitors BEZ235/everolimusA Rose Brannon, Melissa Frizziero, David Chen, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Putative BRAF activating fusion in a medullary thyroid cancerKatayoon Kasaian, Sam M Wiseman, Blair A Walker, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Somatic overgrowth associated with homozygous mutations in both MAN1B1 and SEC23ASwati Gupta, Somayyeh Fahiminiya, Tracy Wang, et al.
Cold Spring Harbor Molecular Case Studies|March 10, 2019
De novo missense variant in the GTPase effector domain (GED) of <i>DNM1L</i> leads to static encephalopathy and seizuresNurit Assia Batzir, Pranjali K Bhagwat, Tanya N Eble, et al.
Cold Spring Harbor Molecular Case Studies|November 18, 2018
A newly identified mutation in the <i>PEX26</i> gene is associated with a milder form of Zellweger spectrum disorderAkemi J Tanaka, Kanji Okumoto, Shigehiko Tamura, et al.
Cold Spring Harbor Molecular Case Studies|February 17, 2021
The gut microbiome: a missing link in understanding the gastrointestinal manifestations of COVID-19?Erin F Brooks, Ami S Bhatt
Cold Spring Harbor Molecular Case Studies|February 11, 2021
A novel variant of <i>CDK19</i> causes a severe neurodevelopmental disorder with infantile spasmsShenghai Yang, Weishi Yu, Qian Chen, et al.
Cold Spring Harbor Molecular Case Studies|March 17, 2017
<i>AIFM1</i> mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infantSarah U Morton, Sanjay P Prabhu, Hart G W Lidov, et al.
Cold Spring Harbor Molecular Case Studies|October 19, 2017
Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1CMari Auranen, Jussi Toppila, Saranya Suriyanarayanan, et al.
Pageof 48