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CD146(+) cells are essential for kidney vasculature development.
Kidney Int. 2016 Aug;90(2):311-324. doi: 10.1016/j.kint.2016.02.021. Epub 2016 Apr 18.
Kidney Int. 2016.
PMID: 27165833
Free article.
Coordination of kidney organogenesis by Wnt signaling.
Halt K, Vainio S.
Halt K, et al.
Pediatr Nephrol. 2014 Apr;29(4):737-44. doi: 10.1007/s00467-013-2733-z. Epub 2014 Jan 21.
Pediatr Nephrol. 2014.
PMID: 24445433
Free PMC article.
Review.
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Functional genetic targeting of embryonic kidney progenitor cells ex vivo.
Junttila S, Saarela U, Halt K, Manninen A, Pärssinen H, Lecca MR, Brändli AW, Sims-Lucas S, Skovorodkin I, Vainio SJ.
Junttila S, et al.
J Am Soc Nephrol. 2015 May;26(5):1126-37. doi: 10.1681/ASN.2013060584. Epub 2014 Sep 8.
J Am Soc Nephrol. 2015.
PMID: 25201883
Free PMC article.
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In vitro induction of nephrogenesis in mouse metanephric mesenchyme with lithium introduction and ureteric bud recombination.
Halt K, Vainio S.
Halt K, et al.
Methods Mol Biol. 2012;886:23-30. doi: 10.1007/978-1-61779-851-1_3.
Methods Mol Biol. 2012.
PMID: 22639248
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Renal blood flow and oxygenation drive nephron progenitor differentiation.
Rymer C, Paredes J, Halt K, Schaefer C, Wiersch J, Zhang G, Potoka D, Vainio S, Gittes GK, Bates CM, Sims-Lucas S.
Rymer C, et al.
Am J Physiol Renal Physiol. 2014 Aug 1;307(3):F337-45. doi: 10.1152/ajprenal.00208.2014. Epub 2014 Jun 11.
Am J Physiol Renal Physiol. 2014.
PMID: 24920757
Free PMC article.
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Severe hospital-acquired hyponatremia in acutely ill children receiving moderately hypotonic fluids.
Lehtiranta S, Honkila M, Kallio M, Halt K, Paalanne N, Pokka T, Tapiainen T.
Lehtiranta S, et al.
Pediatr Nephrol. 2022 Feb;37(2):443-448. doi: 10.1007/s00467-021-05227-0. Epub 2021 Aug 16.
Pediatr Nephrol. 2022.
PMID: 34398305
Free PMC article.
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Correction to: Severe hospital‑acquired hyponatremia in acutely ill children receiving moderately hypotonic fluids.
Lehtiranta S, Honkila M, Kallio M, Halt K, Paalanne N, Pokka T, Tapiainen T.
Lehtiranta S, et al.
Pediatr Nephrol. 2022 Feb;37(2):467. doi: 10.1007/s00467-021-05268-5.
Pediatr Nephrol. 2022.
PMID: 34546420
Free PMC article.
No abstract available.
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Bone marrow failure syndrome caused by homozygous frameshift mutation in the ERCC6L2 gene.
Järviaho T, Halt K, Hirvikoski P, Moilanen J, Möttönen M, Niinimäki R.
Järviaho T, et al.
Clin Genet. 2018 Feb;93(2):392-395. doi: 10.1111/cge.13125. Epub 2017 Dec 18.
Clin Genet. 2018.
PMID: 28815563
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