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Andrew Beenken

Showing results (21-30 of 31) with videos related to

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JCI Insight|April 23, 2026
Failure of endocytic flux in Donnai-Barrow Syndrome caused by LRP2 p.C1400RAndrew Beenken, Tian H Shen, Aryan Ghotra, et al.
American Journal of Physiology. Renal Physiology|September 12, 2024
Spns1 is an iron transporter essential for megalin-dependent endocytosisAndrew Beenken, Tian Shen, Guangchun Jin, et al.
The Journal of Clinical Investigation|July 4, 2008
Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and miceJohn Falardeau, Wilson C J Chung, Andrew Beenken, et al.
Molecular and Cellular Biology|March 7, 2007
Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily membersRegina Goetz, Andrew Beenken, Omar A Ibrahimi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, et al.
Kidney360|February 17, 2026
A Switch in Iron Delivery Is Critical for Postnatal Kidney DevelopmentAndong Qiu, Melanie Viltard, Rong Deng, et al.
JCI Insight|March 1, 2022
Snapshots of nascent RNA reveal cell- and stimulus-specific responses to acute kidney injuryTian Huai Shen, Jacob Stauber, Katherine Xu, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
Nature Communications|October 9, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
JCI Insight|April 23, 2026
Failure of endocytic flux in Donnai-Barrow Syndrome caused by LRP2 p.C1400RAndrew Beenken, Tian H Shen, Aryan Ghotra, et al.
American Journal of Physiology. Renal Physiology|September 12, 2024
Spns1 is an iron transporter essential for megalin-dependent endocytosisAndrew Beenken, Tian Shen, Guangchun Jin, et al.
The Journal of Clinical Investigation|July 4, 2008
Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and miceJohn Falardeau, Wilson C J Chung, Andrew Beenken, et al.
Molecular and Cellular Biology|March 7, 2007
Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily membersRegina Goetz, Andrew Beenken, Omar A Ibrahimi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, et al.
Kidney360|February 17, 2026
A Switch in Iron Delivery Is Critical for Postnatal Kidney DevelopmentAndong Qiu, Melanie Viltard, Rong Deng, et al.
JCI Insight|March 1, 2022
Snapshots of nascent RNA reveal cell- and stimulus-specific responses to acute kidney injuryTian Huai Shen, Jacob Stauber, Katherine Xu, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
Nature Communications|October 9, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.
Pageof 4