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Year | Number of Results |
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2010 | 1 |
2016 | 2 |
2024 | 1 |
PubMed (GeneRIF) for id: 168507
4 results
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PKD1L1 Is Involved in Congenital Chylothorax.
Cells. 2024 Jan 12;13(2):149. doi: 10.3390/cells13020149.
Cells. 2024.
PMID: 38247840
Free PMC article.
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
Vetrini F, D'Alessandro LC, Akdemir ZC, Braxton A, Azamian MS, Eldomery MK, Miller K, Kois C, Sack V, Shur N, Rijhsinghani A, Chandarana J, Ding Y, Holtzman J, Jhangiani SN, Muzny DM, Gibbs RA, Eng CM, Hanchard NA, Harel T, Rosenfeld JA, Belmont JW, Lupski JR, Yang Y.
Vetrini F, et al.
Am J Hum Genet. 2016 Oct 6;99(4):886-893. doi: 10.1016/j.ajhg.2016.07.011. Epub 2016 Sep 8.
Am J Hum Genet. 2016.
PMID: 27616478
Free PMC article.
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Atypical calcium regulation of the PKD2-L1 polycystin ion channel.
DeCaen PG, Liu X, Abiria S, Clapham DE.
DeCaen PG, et al.
Elife. 2016 Jun 27;5:e13413. doi: 10.7554/eLife.13413.
Elife. 2016.
PMID: 27348301
Free PMC article.
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Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR.
Rose JE, et al.
Mol Med. 2010 Jul-Aug;16(7-8):247-53. doi: 10.2119/molmed.2009.00159. Epub 2010 Mar 17.
Mol Med. 2010.
PMID: 20379614
Free PMC article.
Clinical Trial.
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