Pages that link to "Q36106080"

The following pages link to DNA replication stress underlies renal phenotypes in CEP290-associated Joubert syndrome (Q36106080):

Displaying 22 items.

• Ciliogenesis and the DNA damage response: a stressful relationship (Q26747601) (← links)
• Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis (Q28975782) (← links)
• An age of enlightenment for cilia: The FASEB summer research conference on the "Biology of Cilia and Flagella" (Q36495042) (← links)
• Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish (Q37079612) (← links)
• Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish. (Q38669720) (← links)
• Motile and non-motile cilia in human pathology: from function to phenotypes (Q39012190) (← links)
• Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia network (Q39231616) (← links)
• Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome). (Q40398012) (← links)
• Loss of Glis2/NPHP7 causes kidney epithelial cell senescence and suppresses cyst growth in the Kif3a mouse model of cystic kidney disease. (Q41611551) (← links)
• Personalized models reveal mechanistic and therapeutic insights into CEP290-associated Leber congenital amaurosis (Q42370403) (← links)
• A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies (Q47706146) (← links)
• Zfp423/ZNF423 regulates cell cycle progression, the mode of cell division and the DNA-damage response in Purkinje neuron progenitors. (Q47820676) (← links)
• Many Genes-One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders. (Q47833085) (← links)
• Ciliopathies: Replication stress-induced DNA damage in renal ciliopathies. (Q52149805) (← links)
• Urine-derived cells: a promising diagnostic tool in Fabry disease patients (Q57175109) (← links)
• Exploring the Role of Fallopian Ciliated Cells in the Pathogenesis of High-Grade Serous Ovarian Cancer (Q58704255) (← links)
• Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms (Q60638389) (← links)
• Using zebrafish to study the function of nephronophthisis and related ciliopathy genes (Q60920671) (← links)
• Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project (Q64039678) (← links)
• Disease Modeling To Understand the Pathomechanisms of Human Genetic Kidney Disorders (Q90088885) (← links)
• Embryonic and foetal expression patterns of the ciliopathy gene CEP164 (Q92995595) (← links)
• RNA helicase p68 inhibits the transcription and post-transcription of Pkd1 in ADPKD (Q98159124) (← links)