Found: 33
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The immunohistological profile of membranous nephropathy associated with syphilis infection.
- Published in:
- Clinical Kidney Journal, 2021, v. 14, n. 7, p. 1857, doi. 10.1093/ckj/sfab057
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- Publication type:
- Article
APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 8, p. 2327, doi. 10.1007/s00467-021-04960-w
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- Publication type:
- Article
Two cases of fungal cyst infection in ADPKD: is this really a rare complication?
- Published in:
- 2019
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- Publication type:
- journal article
Functional Budd-Chiari Syndrome Associated With Severe Polycystic Liver Disease.
- Published in:
- Clinical Medicine Insights: Gastroenterology, 2017, n. 10, p. 1, doi. 10.1177/1179552217713003
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- Publication type:
- Article
Immunohistochemical detection of polyductin and co-localization with liver progenitor cell markers during normal and abnormal development of the intrahepatic biliary system and in adult hepatobiliary carcinomas.
- Published in:
- Journal of Cellular & Molecular Medicine, 2009, v. 13, n. 7, p. 1279, doi. 10.1111/j.1582-4934.2008.00519.x
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- Publication type:
- Article
WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.
- Published in:
- 2022
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- Publication type:
- Case Study
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney disease.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 3, p. 163, doi. 10.1038/sj.ejhg.5200426
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- Publication type:
- Article
Polyductin, thePKHD1gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm.
- Published in:
- Kidney International, 2004, v. 66, n. 4, p. 1345, doi. 10.1111/j.1523-1755.2004.00844.x
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- Publication type:
- Article
Chikungunya virus as a trigger for different renal disorders: an exploratory study.
- Published in:
- Journal of Nephrology (JNonline), 2022, v. 35, n. 5, p. 1437, doi. 10.1007/s40620-022-01256-6
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- Publication type:
- Article
Age-based ultrasonographic criteria for diagnosis of autosomal dominant polycystic kidney disease in Persian cats.
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- Journal of Feline Medicine & Surgery, 2019, v. 21, n. 2, p. 156, doi. 10.1177/1098612X18764591
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- Publication type:
- Article
Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1.
- Published in:
- Journal of Molecular Medicine, 2014, v. 92, n. 10, p. 1045, doi. 10.1007/s00109-014-1185-7
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- Publication type:
- Article
Influence of androgenic blockade with flutamide on pain behaviour and expression of the genes that encode the NaV1.7 and NaV1.8 voltage-dependent sodium channels in a rat model of postoperative pain.
- Published in:
- 2019
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- Publication type:
- journal article
Caffeine Accelerates Cystic Kidney Disease in a Pkd1-Deficient Mouse Model.
- Published in:
- Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2019, v. 52, n. 5, p. 1061, doi. 10.33594/000000072
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- Publication type:
- Article
Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1940, doi. 10.1093/hmg/ddm141
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- Publication type:
- Article
Polyductin undergoes notch-like processing and regulated release from primary cilia.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 8, p. 942, doi. 10.1093/hmg/ddm039
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- Publication type:
- Article
A novel single amino acid deletion impairs fibronectin function and causes familial glomerulopathy with fibronectin deposits: case report of a family.
- Published in:
- 2019
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- Publication type:
- journal article
Ppia is the most stable housekeeping gene for qRT-PCR normalization in kidneys of three Pkd1-deficient mouse models.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-99366-x
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- Publication type:
- Article
Smoking accelerates renal cystic disease and worsens cardiac phenotype in Pkd1-deficient mice.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-93633-7
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- Publication type:
- Article
Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 4, p. 575
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- Publication type:
- Article
Renal cyst growth is the main determinant for hypertension and concentrating deficit in Pkd1-deficient mice.
- Published in:
- Kidney International, 2014, v. 85, n. 5, p. 1137, doi. 10.1038/ki.2013.501
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- Publication type:
- Article
Infundibular stenosis in Bardet-Biedl syndrome.
- Published in:
- 2011
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- Publication type:
- Case Study
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).
- Published in:
- Human Mutation, 2004, v. 23, n. 5, p. 453, doi. 10.1002/humu.20029
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- Publication type:
- Article
Regulation of CFTR Expression and Arginine Vasopressin Activity Are Dependent on Polycystin-1 in Kidney-Derived Cells.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2016, v. 38, n. 1, p. 28, doi. 10.1159/000438606
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- Publication type:
- Article
Determination of urinary lithogenic parameters in murine models orthologous to autosomal dominant polycystic kidney disease.
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- Urolithiasis, 2014, v. 42, n. 4, p. 301, doi. 10.1007/s00240-014-0664-1
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- Publication type:
- Article
Lipoprotein glomerulopathy associated with the Osaka/Kurashiki APOE variant: two cases identified in Latin America.
- Published in:
- Diagnostic Pathology, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13000-021-01119-x
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- Publication type:
- Article
The effect of sirolimus on angiomyolipoma is determined by decrease of fat-poor compartments and includes striking reduction of vascular structures.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-87930-4
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- Publication type:
- Article
KLOTHO polymorphisms and age-related outcomes in community-dwelling older subjects: The São Paulo Ageing & Health (SPAH) Study.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65441-y
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- Publication type:
- Article
Schistosoma mansoni infection as a trigger to collapsing glomerulopathy in a patient with high-risk APOL1 genotype.
- Published in:
- PLoS Neglected Tropical Diseases, 2020, v. 14, n. 10, p. 1, doi. 10.1371/journal.pntd.0008582
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- Publication type:
- Article
GENETIC ANALYSIS OF A BRAZILIAN NEPHROPATHIC CYSTINOSIS COHORT REVEALS NOVEL CTNS VARIANTS MOSTLY OF NON-EUROPEAN ORIGIN.
- Published in:
- Brazilian Journal of Nephrology / Jornal Brasileiro de Nefrologia, 2021, v. 43, p. 49
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- Publication type:
- Article
CAUSAS MENDELIANAS SAO IDENTIFICADAS COM FREQUENCIA RELATIVAMENTE BAIXA E APRESENTAM UM PERFIL UNICO EM PACIENTES PEDIATRICOS BRASILEIROS COM SINDROME NEFROTICA CORTICO-RESISTENTE E/OU GLOMERULOSCLEROSE SEGMENTAR E FOCAL.
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- Brazilian Journal of Nephrology / Jornal Brasileiro de Nefrologia, 2021, v. 43, p. 49
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- Publication type:
- Article
ANALISE DE MICRORNAS REGULADORES DA EXPRESSAO DE TRANSCRITOS ASSOCIADOS A PLURIPOTENCIA DE CELULAS TRONCO EM MODELOS DE CAMUNDONGOS COM DEFICIENCIA DE PKD1.
- Published in:
- Brazilian Journal of Nephrology / Jornal Brasileiro de Nefrologia, 2021, v. 43, p. 44
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- Publication type:
- Article
FEBRE CHIKUNGUNYA COMO GATILHO PARA DIFERENTES DISTURBIOS RENAIS.
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- Brazilian Journal of Nephrology / Jornal Brasileiro de Nefrologia, 2021, v. 43, p. 34
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- Publication type:
- Article
ANALISE DE MICRORNAS REGULADORES DA EXPRESSAO DE TRANSCRITOS ASSOCIADOS A PLURIPOTENCIA DE CELULAS TRONCO EM MODELOS DE CAMUNDONGOS COM DEFICIENCIA DE PKD1.
- Published in:
- Brazilian Journal of Nephrology / Jornal Brasileiro de Nefrologia, 2021, v. 43, p. 4
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- Publication type:
- Article