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Links from Nucleotide

Items: 4

1.
Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant
Tomohiro Kitano, Shin-ichiro Kitajiri, Shin-ya Nishio, Shin-ichi Usami
Int J Mol Sci. 2019 Sep; 20(18): 4579. Published online 2019 Sep 16. doi: 10.3390/ijms20184579
PMCID:
PMC6769696
AbstractArticlePDF–2.2M
2.
Claudin-14 Gene Polymorphisms and Urine Calcium Excretion
Teresa Arcidiacono, Marco Simonini, Chiara Lanzani, Lorena Citterio, Erika Salvi, Cristina Barlassina, Donatella Spotti, Daniele Cusi, Paolo Manunta, Giuseppe Vezzoli
Clin J Am Soc Nephrol. 2018 Oct 8; 13(10): 1542–1549. Published online 2018 Sep 19. doi: 10.2215/CJN.01770218
PMCID:
PMC6218816
AbstractArticle
3.
Mutations in OTOF, CLDN14 & SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu & Kashmir, India
Nishtha Pandey, Tabassum Rashid, Rajeev Jalvi, Meenakshi Sharma, Raghunath Rangasayee, Khurshid Iqbal Andrabi, Anuranjan Anand
Indian J Med Res. 2017 Oct; 146(4): 489–497. doi: 10.4103/ijmr.IJMR_635_15
PMCID:
PMC5819031
AbstractArticlePDF–1.2M
4.
Claudin-14 regulates renal Ca++ transport in response to CaSR signalling via a novel microRNA pathway
Yongfeng Gong, Vijayaram Renigunta, Nina Himmerkus, Jiaqi Zhang, Aparna Renigunta, Markus Bleich, Jianghui Hou
EMBO J. 2012 Apr 18; 31(8): 1999–2012. Published online 2012 Feb 28. doi: 10.1038/emboj.2012.49
PMCID:
PMC3343334
AbstractArticlePDF–2.2M

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