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A novel loss-of-function mutation of PBK associated with human kidney stone disease.
Sci Rep. 2020 Jun 24;10(1):10282. doi: 10.1038/s41598-020-66936-4.
Sci Rep. 2020.
PMID: 32581305
Free PMC article.
Association between human prothrombin variant (T165M) and kidney stone disease.
Rungroj N, Sudtachat N, Nettuwakul C, Sawasdee N, Praditsap O, Jungtrakoon P, Sritippayawan S, Chuawattana D, Borvornpadungkitti S, Predanon C, Susaengrat W, Yenchitsomanus PT.
Rungroj N, et al. Among authors: praditsap o.
PLoS One. 2012;7(9):e45533. doi: 10.1371/journal.pone.0045533. Epub 2012 Sep 19.
PLoS One. 2012.
PMID: 23029076
Free PMC article.
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A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease.
Rungroj N, Nettuwakul C, Sudtachat N, Praditsap O, Sawasdee N, Sritippayawan S, Chuawattana D, Yenchitsomanus PT.
Rungroj N, et al. Among authors: praditsap o.
BMC Med Genet. 2014 May 2;15:50. doi: 10.1186/1471-2350-15-50.
BMC Med Genet. 2014.
PMID: 24886237
Free PMC article.
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Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease.
Nettuwakul C, Praditsap O, Sawasdee N, Rungroj N, Ruamyod K, Watanapa WB, Junking M, Sangnual S, Sritippayawan S, Cheunsuchon B, Chuawattana D, Rojsatapong S, Chaowagul W, Dib-Hajj SD, Waxman SG, Yenchitsomanus PT.
Nettuwakul C, et al. Among authors: praditsap o.
Sci Rep. 2018 Jul 11;8(1):10453. doi: 10.1038/s41598-018-28623-3.
Sci Rep. 2018.
PMID: 29992996
Free PMC article.
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An induced pluripotent stem cell line (MUSIi019-A) generated from a patient with distal renal tubular acidosis carrying a compound heterozygous mutation in solute carrier family 4 member 1 (SLC4A1) gene.
Kaewboonlert N, Wattanapanitch M, Praditsap O, Deejai N, Chanprasert C, Sawasdee N, Nettuwakul C, Wanachiwanawin W, Sritippayawan S, Thamtarana PJ, Yenchitsomanus PT, Rungroj N.
Kaewboonlert N, et al. Among authors: praditsap o.
Stem Cell Res. 2023 Mar;67:103043. doi: 10.1016/j.scr.2023.103043. Epub 2023 Feb 10.
Stem Cell Res. 2023.
PMID: 36791635
Free article.
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Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome.
Kantaputra P, Guven Y, Kalayci T, Özer PK, Panyarak W, Intachai W, Olsen B, Carlson BM, Praditsap O, Tongsima S, Ngamphiw C, Jatooratthawichot P, Tucker AS, Ketudat Cairns JR.
Kantaputra P, et al. Among authors: praditsap o.
Clin Genet. 2022 Jul;102(1):66-71. doi: 10.1111/cge.14134. Epub 2022 Mar 31.
Clin Genet. 2022.
PMID: 35352826
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A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5.
Kantaputra PN, Pongprot Y, Praditsap O, Pho-iam T, Limwongse C.
Kantaputra PN, et al. Among authors: praditsap o.
Am J Med Genet A. 2003 Jul 30;120A(3):381-5. doi: 10.1002/ajmg.a.20040.
Am J Med Genet A. 2003.
PMID: 12838559
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