Cargando…

Differential Expression of PKD2-Associated Genes in Autosomal Dominant Polycystic Kidney Disease

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by formation of multiple fluid-filled cysts that expand over time and destroy renal architecture. The proteins encoded by the PKD1 and PKD2 genes, mutations in which account for nearly all cases of ADPKD, may help guard against cy...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yook, Yeon Joo, Woo, Yu Mi, Yang, Moon Hee, Ko, Je Yeong, Kim, Bo Hye, Lee, Eun Ji, Chang, Eun Sun, Lee, Min Joo, Lee, Sunyoung, Park, Jong Hoon
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korea Genome Organization 2012
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475485/ https://www.ncbi.nlm.nih.gov/pubmed/23105924 http://dx.doi.org/10.5808/GI.2012.10.1.16

Ejemplares similares

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

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

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 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)

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)

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

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)

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)

Polycystin-1 Expression in Fetal, Adult and Autosomal Dominant Polycystic Kidney
por: Chae, Seoung Wan, et al.
Publicado: (2006)

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

Factors Associated With the Development and Severity of Polycystic Liver in Patients With Autosomal Dominant Polycystic Kidney Disease
por: Kim, Yaerim, et al.
Publicado: (2023)

Autosomal dominant polycystic kidney
por: Gudadhe, Rugaved Raghavendra, et al.
Publicado: (2022)

Pain and Obesity in Autosomal Dominant Polycystic Kidney Disease: A Post Hoc Analysis of the Halt Progression of Polycystic Kidney Disease (HALT-PKD) Studies
por: Nowak, Kristen L., et al.
Publicado: (2021)

Long-term Tolvaptan Treatment of Autosomal Dominant Polycystic Kidney Disease in Korea
por: Kim, Ha Yeon, et al.
Publicado: (2018)

Clinical Correlates of Mass Effect in Autosomal Dominant Polycystic Kidney Disease
por: Kim, Hyunsuk, et al.
Publicado: (2015)

A Non-Synonymous Mutation in the Canine Pkd1 Gene Is Associated with Autosomal Dominant Polycystic Kidney Disease in Bull Terriers
por: Gharahkhani, Puya, et al.
Publicado: (2011)

Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction
por: He, Wen-Bin, et al.
Publicado: (2018)

Safety and efficacy of Tolvaptan in real-world patients with autosomal dominant polycystic kidney disease- interim results of SLOW-PKD surveillance
por: Mochizuki, Toshio, et al.
Publicado: (2021)

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)

Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease
por: Ebner, Kathrin, et al.
Publicado: (2017)

Obturator hernia in autosomal dominant polycystic kidney disease
por: Jung, Jong Hwan, et al.
Publicado: (2018)

PKD1 Duplicated regions limit clinical Utility of Whole Exome Sequencing for Genetic Diagnosis of Autosomal Dominant Polycystic Kidney Disease
por: Ali, Hamad, et al.
Publicado: (2019)

PKD1-associated autosomal dominant polycystic kidney disease with glomerular cysts presenting with nephrotic syndrome caused by focal segmental glomerulosclerosis
por: Oda, Yasuhiro, et al.
Publicado: (2019)

GANAB and PKD1 Variations in a 12 Years Old Female Patient With Early Onset of Autosomal Dominant Polycystic Kidney Disease
por: Waldrop, Elizabeth, et al.
Publicado: (2019)

Identification of novel PKD1 mutations in two Chinese families with autosomal dominant polycystic kidney disease by targeted next generation sequencing
por: Liu, Qun, et al.
Publicado: (2020)

A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease
por: Zhao, Qianying, et al.
Publicado: (2023)

Suppression of Foxo3-Gatm by miR-132-3p Accelerates Cyst Formation by Up-Regulating ROS in Autosomal Dominant Polycystic Kidney Disease
por: Choi, Seonju, et al.
Publicado: (2021)

Femoral Neuropathy Secondary to Autosomal Dominant Polycystic Kidney Disease: A Case Report
por: Yoo, Jeehyun, et al.
Publicado: (2018)

Unilateral renal displacement in an autosomal dominant polycystic kidney disease patient
por: Kim, Jin, et al.
Publicado: (2023)

Autosomal dominant polycystic kidney disease in Colombia
por: Camargo, Jessica T., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_he6gkoulbu1kd93f6naco4gg4j