Found: 24
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Toxigenic Corynebacterium diphtheriae-Associated Genital Ulceration.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic Treatment.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 17, p. 6093, doi. 10.3390/ijms21176093
- By:
- Publication type:
- Article
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality.
- Published in:
- Molecular & Cellular Pediatrics, 2021, v. 8, n. 1, p. 1, doi. 10.1186/s40348-021-00111-1
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- Publication type:
- Article
Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT).
- Published in:
- Molecular & Cellular Pediatrics, 2021, v. 8, n. 1, p. 1, doi. 10.1186/s40348-021-00112-0
- By:
- Publication type:
- Article
Dysregulated Autophagy Contributes to Podocyte Damage in Fabry’s Disease
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0063506
- By:
- Publication type:
- Article
The Centrosomal Kinase Plk1 Localizes to the Transition Zone of Primary Cilia and Induces Phosphorylation of Nephrocystin-1.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038838
- By:
- Publication type:
- Article
Erbliche Zystennierenerkrankungen: Autosomal-dominante und autosomal-rezessive polyzystische Nierenerkrankung (ADPKD und ARPKD).
- Published in:
- Medizinische Genetik, 2018, v. 30, n. 4, p. 422, doi. 10.1007/s11825-018-0224-0
- By:
- Publication type:
- Article
AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosis.
- Published in:
- EMBO Journal, 2012, v. 31, n. 20, p. 3961, doi. 10.1038/emboj.2012.236
- By:
- Publication type:
- Article
Implications of early diagnosis of autosomal dominant polycystic kidney disease: A post hoc analysis of the TEMPO 3:4 trial.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-61303-9
- By:
- Publication type:
- Article
ATRT-07. TARGETING PRIMARY CILIOGENESIS IN ATYPICAL TERATOID/RHABDOID TUMORS.
- Published in:
- Neuro-Oncology, 2019, v. 21, p. ii64, doi. 10.1093/neuonc/noz036.006
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- Publication type:
- Article
Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases.
- Published in:
- 2022
- By:
- Publication type:
- journal article
The carboxy‐terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC‐activation.
- Published in:
- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 24, p. 14633, doi. 10.1111/jcmm.16014
- By:
- Publication type:
- Article
IL-6/Smad2 signaling mediates acute kidney injury and regeneration in a murine model of neonatal hyperoxia.
- Published in:
- FASEB Journal, 2019, v. 33, n. 5, p. 5887, doi. 10.1096/fj.201801875RR
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- Publication type:
- Article
Differential regulation of MYC expression by PKHD1/Pkhd1 in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease.
- Published in:
- Frontiers in Cell & Developmental Biology, 2023, p. 1, doi. 10.3389/fcell.2023.1270980
- By:
- Publication type:
- Article
Unmet needs and challenges for follow-up and treatment of autosomal dominant polycystic kidney disease: the paediatric perspective.
- Published in:
- Clinical Kidney Journal, 2018, v. 11, p. i14, doi. 10.1093/ckj/sfy088
- By:
- Publication type:
- Article
Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4.
- Published in:
- Clinical Infectious Diseases, 2017, v. 64, n. 12, p. 1637, doi. 10.1093/cid/cix218
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- Publication type:
- Article
Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease.
- Published in:
- BMC Nephrology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12882-023-03072-x
- By:
- Publication type:
- Article
Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease.
- Published in:
- BMC Nephrology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12882-023-03072-x
- By:
- Publication type:
- Article
NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway.
- Published in:
- Journal of Cell Biology, 2011, v. 193, n. 4, p. 633, doi. 10.1083/jcb.201009069
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- Publication type:
- Article
Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature Reviews.
- Published in:
- JAMA Pediatrics, 2018, v. 172, n. 1, p. 74, doi. 10.1001/jamapediatrics.2017.3938
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- Publication type:
- Article
Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoring.
- Published in:
- Pediatric Nephrology, 2018, v. 33, n. 4, p. 619, doi. 10.1007/s00467-017-3846-6
- By:
- Publication type:
- Article
Primary cilia contribute to the aggressiveness of atypical teratoid/rhabdoid tumors.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 9, p. 1, doi. 10.1038/s41419-022-05243-4
- By:
- Publication type:
- Article
Enzyme Replacement Therapy Clears Gb3 Deposits from a Podocyte Cell Culture Model of Fabry Disease but Fails to Restore Altered Cellular Signaling.
- Published in:
- Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2019, v. 52, n. 5, p. 1139, doi. 10.33594/000000077
- By:
- Publication type:
- Article