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Filipa M Lopes

Showing results (11-20 of 22) with videos related to

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Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
Elife|July 11, 2024
Human <i>HPSE2</i> gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndromeFilipa M Lopes, Celine Grenier, Benjamin W Jarvis, et al.
Kidney International Reports|July 13, 2023
Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder DiseaseCeline Grenier, Filipa M Lopes, Anna M Cueto-González, et al.
Stem Cell Reports|May 24, 2024
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformationsIoannis Bantounas, Kirsty M Rooney, Filipa M Lopes, et al.
Scientific Reports|July 31, 2021
Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladderEmad A Hindi, Craig J Williams, Leo A H Zeef, et al.
Kidney International|March 20, 2019
Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladderNeil A Roberts, Emma N Hilton, Filipa M Lopes, et al.
Frontiers in Genetics|July 11, 2022
Expanding the <i>HPSE2</i> Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary BladderGlenda M Beaman, Filipa M Lopes, Aybike Hofmann, et al.
Elife|September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valvesMelanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
The Journal of Clinical Investigation|September 13, 2019
Loss-of-function variants in myocardin cause congenital megabladder in humans and miceArjan C Houweling, Glenda M Beaman, Alex V Postma, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

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Pageof 3
Frontiers in Cell and Developmental Biology|August 22, 2025
Haploinsufficiency of <i>ABL1</i> is associated with dominant isolated omphaloceleCaroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, et al.
Elife|July 11, 2024
Human <i>HPSE2</i> gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndromeFilipa M Lopes, Celine Grenier, Benjamin W Jarvis, et al.
Kidney International Reports|July 13, 2023
Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder DiseaseCeline Grenier, Filipa M Lopes, Anna M Cueto-González, et al.
Stem Cell Reports|May 24, 2024
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformationsIoannis Bantounas, Kirsty M Rooney, Filipa M Lopes, et al.
Scientific Reports|July 31, 2021
Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladderEmad A Hindi, Craig J Williams, Leo A H Zeef, et al.
Kidney International|March 20, 2019
Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladderNeil A Roberts, Emma N Hilton, Filipa M Lopes, et al.
Frontiers in Genetics|July 11, 2022
Expanding the <i>HPSE2</i> Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary BladderGlenda M Beaman, Filipa M Lopes, Aybike Hofmann, et al.
Elife|September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valvesMelanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
The Journal of Clinical Investigation|September 13, 2019
Loss-of-function variants in myocardin cause congenital megabladder in humans and miceArjan C Houweling, Glenda M Beaman, Alex V Postma, et al.
American Journal of Human Genetics|May 4, 2019
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract ObstructionCaroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, et al.
Pageof 3