Reduction of elevated Gli3 does not alter the progression of autosomal recessive polycystic kidney disease
Fuente:
Wiley Open Access
Saved in:
| Main Authors: | Lauren G. Russell, Maria Kolatsi‐Joannou, Laura Wilson, Jennifer C. Chandler, Nuria Perretta Tejedor, Georgie Stagg, Karen L. Price, Christopher J. Rowan, Tessa Crompton, Norman D. Rosenblum, Paul J. D. Winyard, David A. Long |
|---|---|
| Format: | Artículo Open Access |
| Published: |
Wiley
2025
|
| Subjects: | |
| Online Access: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
Cardiac connections: Effects on the heart as a result of autosomal recessive polycystic kidney disease
by: Sheina Franco, et al.
Published: (2025)
by: Sheina Franco, et al.
Published: (2025)
A proposed classification for standardized reporting of liver disease in children with autosomal recessive polycystic kidney disease
by: Kavya Kurkal, et al.
Published: (2026)
by: Kavya Kurkal, et al.
Published: (2026)
Concomitant Wilms tumor and autosomal dominant polycystic kidney disease
by: Andrew M. Fleming, et al.
Published: (2024)
by: Andrew M. Fleming, et al.
Published: (2024)
Massive bilateral renomegaly: severe expression of autosomal dominant polycystic kidney disease
by: Vianey Guadalupe Tellez Bolaños
Published: (2023)
by: Vianey Guadalupe Tellez Bolaños
Published: (2023)
Altered bile acid and coproporphyrin‐I disposition in patients with autosomal dominant polycystic kidney disease
by: Jacqueline B. Tiley, et al.
Published: (2024)
by: Jacqueline B. Tiley, et al.
Published: (2024)
Global analysis of urinary extracellular vesicle small RNAs in autosomal dominant polycystic kidney disease
by: Hamad Ali, et al.
Published: (2024)
by: Hamad Ali, et al.
Published: (2024)
Chronic brucellosis with hepatic brucelloma and AA amyloidosis in a patient with autosomal dominant polycystic kidney disease
by: Arpitha Kollabathula
Published: (2020)
by: Arpitha Kollabathula
Published: (2020)
Acute coronary syndrome in patients with autosomal dominant polycystic kidney disease: a systematic review and meta‐analysis
by: Ashraf Ahmed, et al.
Published: (2025)
by: Ashraf Ahmed, et al.
Published: (2025)
The screening, diagnosis, and management of patients with autosomal dominant polycystic kidney disease: A national consensus statement from Taiwan
by: Pao‐Wen Yen, et al.
Published: (2024)
by: Pao‐Wen Yen, et al.
Published: (2024)
Revisiting the gene mutations and protein profile of WT 9‐12: An autosomal dominant polycystic kidney disease cell line
by: Hwa Chia Chai, et al.
Published: (2024)
by: Hwa Chia Chai, et al.
Published: (2024)
Caring for Australians and New ZealandeRs with kidney Impairment guideline commentary on kidney disease: improving global outcomes 2025 guidelines for diagnosis and management of autosomal polycystic kidney disease
by: Mia E. Abdy, et al.
Published: (2026)
by: Mia E. Abdy, et al.
Published: (2026)
Single‐cell transcriptomics identifies aberrant glomerular angiogenic signalling in the early stages of WT1 kidney disease
by: Jennifer C Chandler, et al.
Published: (2024)
by: Jennifer C Chandler, et al.
Published: (2024)
Index cases of intracranial aneurysms in autosomal dominant polycystic kidney disease: longitudinal experience from a single renal transplantation centre
by: Joel Ern Zher Chan, et al.
Published: (2025)
by: Joel Ern Zher Chan, et al.
Published: (2025)
ALOXE3 missense variant in a Chihuahua with autosomal recessive ichthyosis
by: Carina Vinberg, et al.
Published: (2025)
by: Carina Vinberg, et al.
Published: (2025)
Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegia
by: Yusen Qiu, et al.
Published: (2024)
by: Yusen Qiu, et al.
Published: (2024)
Next-generation whole-exome sequencing contribution to identification of rare autosomal recessive diseases
by: Tautvydas Rančelis
Published: (2013)
by: Tautvydas Rančelis
Published: (2013)
Treatment of autosomal recessive congenital ichthyosis caused by a NIPAL4 variant with upadacitinib
by: Zhuoqing Gong, et al.
Published: (2024)
by: Zhuoqing Gong, et al.
Published: (2024)
Glycolytic alterations as biomarkers in polycystic kidney disease: A study using a PKD1 knockout model in NRK ‐ 52E rat kidney epithelial cells
by: Ida Kjær Mieritz, et al.
Published: (2026)
by: Ida Kjær Mieritz, et al.
Published: (2026)
Identification of drug repurposing candidates for the treatment of polycystic kidney disease
by: Alina Meyer, et al.
Published: (2026)
by: Alina Meyer, et al.
Published: (2026)
Vortex lattices and critical fields in anisotropic superconductors
by: Speight, Martin, et al.
Published: (2024)
by: Speight, Martin, et al.
Published: (2024)
Short range intervortex forces
by: Speight, Martin, et al.
Published: (2025)
by: Speight, Martin, et al.
Published: (2025)
Dependencia y cooperación entre los sentidos
by: Lawrence D. Rosenblum
Published: (2013)
by: Lawrence D. Rosenblum
Published: (2013)
A New Curriculum for a New Age
by: Crompton, Marielizabeth
Published: (2004)
by: Crompton, Marielizabeth
Published: (2004)
The Potential of Artificial Intelligence in Higher Education
by: Helen Crompton
Published: (2021)
by: Helen Crompton
Published: (2021)
A novel case of autosomal recessive CARD11 loss‐of‐function underlying impaired antiviral immunity and a review of literature
by: Hamish Anderson, et al.
Published: (2026)
by: Hamish Anderson, et al.
Published: (2026)
Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy
by: Sandra Donkervoort, et al.
Published: (2024)
by: Sandra Donkervoort, et al.
Published: (2024)
The first Chinese intellectual developmental disorder, autosomal recessive 57 patient with two novel MBOAT7 variants
by: Huimin Li, et al.
Published: (2024)
by: Huimin Li, et al.
Published: (2024)
Novel compound heterozygous variants in the TSPEAR gene causing autosomal recessive hearing loss in a Chinese family
by: Xinyu Shi, et al.
Published: (2024)
by: Xinyu Shi, et al.
Published: (2024)
Novel compound heterozygous variants in MARVELD2 causing autosomal recessive hearing loss in two Chinese families
by: Xinyu Shi, et al.
Published: (2024)
by: Xinyu Shi, et al.
Published: (2024)
Response to the correspondence on “Performance of single‐gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting”
by: Julia Wynn, et al.
Published: (2024)
by: Julia Wynn, et al.
Published: (2024)
Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal‐recessive hypophosphataemic rickets type 2
by: Fatma Dursun, et al.
Published: (2024)
by: Fatma Dursun, et al.
Published: (2024)
A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing
by: Bianca R. Grosz, et al.
Published: (2024)
by: Bianca R. Grosz, et al.
Published: (2024)
A capture‐based method of prenatal cell‐free DNA screening for autosomal recessive non‐syndromic hearing loss
by: Qian Mu, et al.
Published: (2024)
by: Qian Mu, et al.
Published: (2024)
Contribution of alterations in peritubular capillary density and microcirculation to the progression of tubular injury and kidney fibrosis
by: Zhengrong Ren, et al.
Published: (2025)
by: Zhengrong Ren, et al.
Published: (2025)
Automated identification of earthen berms in Western US rangelands from LiDAR‐based digital elevation models
by: Haiqing Xu, et al.
Published: (2024)
by: Haiqing Xu, et al.
Published: (2024)
Heterozygous loss of function variants in IFT140 are associated with polycystic kidney disease
by: Dinah Clark, et al.
Published: (2024)
by: Dinah Clark, et al.
Published: (2024)
La adopción de los recursos educativos abiertos: un continuo de práctica abierta
by: Adrian Stagg
Published: (2014)
by: Adrian Stagg
Published: (2014)
Redes y difusión del conocimiento: ¿Es posible reinsertar a la economía dentro de las ciencias humanas, a través del paradigma de la complejidad?
by: Marcial Stagg
Published: (2011)
by: Marcial Stagg
Published: (2011)
Clinical, genetic, and neuroimaging profiles of autosomal recessive spinocerebellar ataxia type 4 caused by novel VPS13D variants in Chinese
by: Yue Dong, et al.
Published: (2024)
by: Yue Dong, et al.
Published: (2024)
Towards a universal phase diagram of planar chiral magnets
by: Schroers, Bernd, et al.
Published: (2025)
by: Schroers, Bernd, et al.
Published: (2025)
Similar Items
-
Cardiac connections: Effects on the heart as a result of autosomal recessive polycystic kidney disease
by: Sheina Franco, et al.
Published: (2025) -
A proposed classification for standardized reporting of liver disease in children with autosomal recessive polycystic kidney disease
by: Kavya Kurkal, et al.
Published: (2026) -
Concomitant Wilms tumor and autosomal dominant polycystic kidney disease
by: Andrew M. Fleming, et al.
Published: (2024) -
Massive bilateral renomegaly: severe expression of autosomal dominant polycystic kidney disease
by: Vianey Guadalupe Tellez Bolaños
Published: (2023) -
Altered bile acid and coproporphyrin‐I disposition in patients with autosomal dominant polycystic kidney disease
by: Jacqueline B. Tiley, et al.
Published: (2024)