Cargando…

Enhanced β-adrenergic response in mice with dominant-negative expression of the PKD2L1 channel

Polycystic kidney disease (PKD) is the most common genetic cause of kidney failure in humans. Among the various PKD-related molecules, PKD2L1 forms cation channels, but its physiological importance is obscure. In the present study, we established a transgenic mouse line by overexpressing the dominan...

Descripción completa

Detalles Bibliográficos
Autores principales:	Murakami, Manabu, Murakami, Agnieszka M., Nemoto, Takayuki, Ohba, Takayoshi, Yonekura, Manabu, Toyama, Yuichi, Tomita, Hirofumi, Matsuzaki, Yasushi, Sawamura, Daisuke, Hirota, Kazuyoshi, Itagaki, Shirou, Asada, Yujiro, Miyoshi, Ichiro
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775249/ https://www.ncbi.nlm.nih.gov/pubmed/35051185 http://dx.doi.org/10.1371/journal.pone.0261668

Ejemplares similares

Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice
por: Murakami, Manabu, et al.
Publicado: (2020)

Attenuated β-adrenergic response in calcium/calmodulin-dependent protein kinase IV-knockout mice
por: Murakami, Manabu, et al.
Publicado: (2021)

A simple, dual direct expression plasmid system in prokaryotic and mammalian cells
por: Murakami, Manabu, et al.
Publicado: (2023)

A simple and dual expression plasmid system in prokaryotic (E. coli) and mammalian cells
por: Murakami, Manabu, et al.
Publicado: (2019)

A dual prokaryotic (E. coli) expression system (pdMAX)
por: Murakami, Manabu, et al.
Publicado: (2021)

A novel binding site between the voltage-dependent calcium channel Ca(V)1.2 subunit and Ca(V)β2 subunit discovered using a new analysis method for protein–protein interactions
por: Murakami, Agnieszka M., et al.
Publicado: (2023)

PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease
por: Vouk, Katja, et al.
Publicado: (2006)

Monkeys mutant for PKD1 recapitulate human autosomal dominant polycystic kidney disease
por: Tsukiyama, Tomoyuki, et al.
Publicado: (2019)

PKD1 Mutation Is a Biomarker for Autosomal Dominant Polycystic Kidney Disease
por: Kimura, Tomoki, et al.
Publicado: (2023)

Identification of novel PKD1 and PKD2 mutations in Korean patients with autosomal dominant polycystic kidney disease
por: Choi, Rihwa, et al.
Publicado: (2014)

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease
por: Liu, Bei, et al.
Publicado: (2015)

Prediction of Renal Prognosis in Patients with Autosomal Dominant Polycystic Kidney Disease Using PKD1/PKD2 Mutations
por: Kataoka, Hiroshi, et al.
Publicado: (2020)

Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencing
por: Trujillano, Daniel, et al.
Publicado: (2014)

Corrigendum: Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease
por: Liu, Bei, et al.
Publicado: (2016)

Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD)
por: Carrera, Paola, et al.
Publicado: (2016)

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease – a case report
por: Elisakova, Veronika, et al.
Publicado: (2018)

Stromal interaction molecule 1 haploinsufficiency causes maladaptive response to pressure overload
por: Ohba, Takayoshi, et al.
Publicado: (2017)

Pkd1 and Pkd2 Are Required for Normal Placental Development
por: Garcia-Gonzalez, Miguel A., et al.
Publicado: (2010)

Differential Expression of PKD2-Associated Genes in Autosomal Dominant Polycystic Kidney Disease
por: Yook, Yeon Joo, et al.
Publicado: (2012)

Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease
por: Obeidova, Lena, et al.
Publicado: (2014)

Autosomal Dominant Polycystic Kidney Disease: Presence of Hypomorphic Alleles in PKD1 Gene
por: Pandita, S., et al.
Publicado: (2018)

Prediction of municipality-level winter wheat yield based on meteorological data using machine learning in Hokkaido, Japan
por: Murakami, Keach, et al.
Publicado: (2021)

New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease
por: Stekrova, Jitka, et al.
Publicado: (2009)

A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease
por: Jamshidi, Javad, et al.
Publicado: (2016)

Exon Sequencing of PKD1 Gene in an Iranian Patient with Autosomal-Dominant Polycystic Kidney Disease
por: Hafizi, Atousa, et al.
Publicado: (2014)

Hypomorphic PKD1 Alleles Impact Disease Variability in Autosomal Dominant Polycystic Kidney Disease
por: Gulati, Ashima, et al.
Publicado: (2023)

Modifiers of Autosomal Dominant Polycystic Kidney Disease Severity: The Role of PKD1 Hypomorphic Alleles
por: Ambrosini, Enrico, et al.
Publicado: (2023)

Novel method for the genomic analysis of PKD1 mutation in autosomal dominant polycystic kidney disease
por: Shang, Shunlai, et al.
Publicado: (2023)

A novel PKD1 variant demonstrates a disease-modifying role in trans with a truncating PKD1 mutation in patients with Autosomal Dominant Polycystic Kidney Disease
por: Ali, Hamad, et al.
Publicado: (2015)

High Resolution Melt analysis for mutation screening in PKD1 and PKD2
por: Bataille, Stanislas, et al.
Publicado: (2011)

Concerns for labor analgesia and autism spectrum disorders
por: Saito, Manabu, et al.
Publicado: (2020)

A Novel PKD1 Mutation Associated With Autosomal Dominant Kidney Disease and Cerebral Cavernous Malformation
por: Thomas, Christian, et al.
Publicado: (2018)

p53 mutation regulates PKD genes and results in co-occurrence of PKD and tumorigenesis
por: Li, Haili, et al.
Publicado: (2019)

Technical Evaluation: Identification of Pathogenic Mutations in PKD1 and PKD2 in Patients with Autosomal Dominant Polycystic Kidney Disease by Next-Generation Sequencing and Use of a Comprehensive New Classification System
por: Kinoshita, Moritoshi, et al.
Publicado: (2016)

PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data()
por: Entezam, Mona, et al.
Publicado: (2016)

Establishing community-based integrated care for elderly patients through interprofessional teamwork: a qualitative analysis
por: Asakawa, Tomohiro, et al.
Publicado: (2017)

AKAP13 Rho-GEF and PKD-Binding Domain Deficient Mice Develop Normally but Have an Abnormal Response to β-Adrenergic-Induced Cardiac Hypertrophy
por: Spindler, Matthew J., et al.
Publicado: (2013)

Polycystic Kidney Disease Caused by Bilineal Inheritance of Truncating PKD1 as Well as PKD2 Mutations
por: Losekoot, Monique, et al.
Publicado: (2020)

PKD1 and PKD2 mRNA cis-inhibition drives polycystic kidney disease progression
por: Lakhia, Ronak, et al.
Publicado: (2022)

Geospatial and temporal associations of Getah virus circulation among pigs and horses around the perimeter of outbreaks in Japanese racehorses in 2014 and 2015
por: Bannai, Hiroshi, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_b0op1jjcb9dpbfqncdhq2hgn2u