Found: 9
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Association between Human Prothrombin Variant (T165M) and Kidney Stone Disease.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045533
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- Article
A novel splice-acceptor site mutation (IVS13-2A>T) of polycystic kidney disease 1 ( PKD1) gene resulting in an RNA processing defect with a 74-nucleotide deletion in exon 14 of the mRNA transcript.
- Published in:
- Human Mutation, 2000, v. 15, n. 1, p. 115, doi. 10.1002/(SICI)1098-1004(200001)15:1<115::AID-HUMU22>3.0.CO;2-Z
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- Article
Association between intelectin-1 variation and human kidney stone disease in northeastern Thai population.
- Published in:
- Urolithiasis, 2021, v. 49, n. 6, p. 521, doi. 10.1007/s00240-021-01267-1
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- Article
Correlation between genotypes of F2 rs5896 (p.Thr165Met) polymorphism and urinary prothrombin fragment 1.
- Published in:
- Urolithiasis, 2018, v. 46, n. 4, p. 405, doi. 10.1007/s00240-017-0981-2
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- Article
Evidence suggesting a genetic contribution to kidney stone in northeastern Thai population.
- Published in:
- Urological Research, 2009, v. 37, n. 3, p. 141, doi. 10.1007/s00240-009-0189-1
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- Article
A novel loss-of-function mutation of PBK associated with human kidney stone disease.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66936-4
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- Article
Molecular Diagnosis of Solute Carrier Family 4 Member 1 (SLC4A1) Mutation–Related Autosomal Recessive Distal Renal Tubular Acidosis.
- Published in:
- Laboratory Medicine, 2019, v. 50, n. 1, p. 78, doi. 10.1093/labmed/lmy051
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- Article
A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease.
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-50
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- Article
Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP).
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- BMC Medical Genetics, 2004, v. 5, p. 1
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- Publication type:
- Article