PubMed for id: 155969705

Year	Number of Results
1994	1
1995	1
1996	1
1997	1
2000	1
2019	1
2020	1
2021	1
2022	1
2023	2
2024	0

1

Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss.

Yun Y, Park SS, Lee S, Seok H, Park S, Lee SY. Yun Y, et al. Int J Mol Sci. 2023 Dec 3;24(23):17077. doi: 10.3390/ijms242317077. Int J Mol Sci. 2023. PMID: 38069401 Free PMC article.

2

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.

Tschernoster N, Erger F, Kohl S, Reusch B, Wenzel A, Walsh S, Thiele H, Becker C, Franitza M, Bartram MP, Kömhoff M, Schumacher L, Kukat C, Borodina T, Quedenau C, Nürnberg P, Rinschen MM, Driller JH, Pedersen BP, Schlingmann KP, Hüttel B, Bockenhauer D, Beck B, Altmüller J. Tschernoster N, et al. Genome Med. 2023 Aug 23;15(1):62. doi: 10.1186/s13073-023-01215-1. Genome Med. 2023. PMID: 37612755 Free PMC article.

3

A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis.

Zhao Q, Xiang Q, Tan Y, Xiao X, Xie H, Wang H, Yang M, Liu S. Zhao Q, et al. Mol Genet Genomic Med. 2022 Oct;10(10):e2027. doi: 10.1002/mgg3.2027. Epub 2022 Aug 1. Mol Genet Genomic Med. 2022. PMID: 35913199 Free PMC article.

4

Simultaneous Homozygous Mutations in SLC12A3 and CLCNKB in an Inbred Chinese Pedigree.

Mou L, Wu F. Mou L, et al. Genes (Basel). 2021 Mar 5;12(3):369. doi: 10.3390/genes12030369. Genes (Basel). 2021. PMID: 33807568 Free PMC article.

5

Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3.

Han Y, Cheng H, Shao S, Lang Y, Zhao X, Lin Y, Wang S, Shi X, Liu Z, Shao L. Han Y, et al. Endocrine. 2020 Apr;68(1):192-202. doi: 10.1007/s12020-019-02156-9. Epub 2019 Dec 13. Endocrine. 2020. PMID: 31834604

6

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Konrad M, Vollmer M, Lemmink HH, VAN DEN Heuvel LPWJ, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NVAM, Seyberth HW, Feldmann D, Hildebrandt F. Konrad M, et al. J Am Soc Nephrol. 2000 Aug;11(8):1449-1459. doi: 10.1681/ASN.V1181449. J Am Soc Nephrol. 2000. PMID: 10906158

7

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP. Simon DB, et al. Nat Genet. 1997 Oct;17(2):171-8. doi: 10.1038/ng1097-171. Nat Genet. 1997. PMID: 9326936

8

Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization.

Saito-Ohara F, Uchida S, Takeuchi Y, Sasaki S, Hayashi A, Marumo F, Ikeuchi T. Saito-Ohara F, et al. Genomics. 1996 Sep 1;36(2):372-4. doi: 10.1006/geno.1996.0479. Genomics. 1996. PMID: 8812470 No abstract available.

9

Cloning, tissue distribution, and intrarenal localization of ClC chloride channels in human kidney.

Takeuchi Y, Uchida S, Marumo F, Sasaki S. Takeuchi Y, et al. Kidney Int. 1995 Nov;48(5):1497-503. doi: 10.1038/ki.1995.439. Kidney Int. 1995. PMID: 8544406 Free article.

10

Two highly homologous members of the ClC chloride channel family in both rat and human kidney.

Kieferle S, Fong P, Bens M, Vandewalle A, Jentsch TJ. Kieferle S, et al. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):6943-7. doi: 10.1073/pnas.91.15.6943. Proc Natl Acad Sci U S A. 1994. PMID: 8041726 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

10 results

Results by year