PubMed (OMIM) for id: 7480

Year	Number of Results
1970	1
1971	1
1976	1
1987	1
1988	1
1989	1
1997	2
2000	1
2001	1
2002	1
2006	1
2008	1
2010	2
2016	1
2018	1
2020	1
2024	0

1

Parathyroid hormone-dependent bone formation requires butyrate production by intestinal microbiota.

Li JY, Yu M, Pal S, Tyagi AM, Dar H, Adams J, Weitzmann MN, Jones RM, Pacifici R. Li JY, et al. J Clin Invest. 2020 Apr 1;130(4):1767-1781. doi: 10.1172/JCI133473. J Clin Invest. 2020. PMID: 31917685 Free PMC article.

2

Split hand-foot malformation and a novel WNT10B mutation.

Kantaputra PN, Kapoor S, Verma P, Intachai W, Ketudat Cairns JR. Kantaputra PN, et al. Eur J Med Genet. 2018 Jul;61(7):372-375. doi: 10.1016/j.ejmg.2018.02.001. Epub 2018 Feb 7. Eur J Med Genet. 2018. PMID: 29427788

3

Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Yu P, Yang W, Han D, Wang X, Guo S, Li J, Li F, Zhang X, Wong SW, Bai B, Liu Y, Du J, Sun ZS, Shi S, Feng H, Cai T. Yu P, et al. Am J Hum Genet. 2016 Jul 7;99(1):195-201. doi: 10.1016/j.ajhg.2016.05.012. Epub 2016 Jun 16. Am J Hum Genet. 2016. PMID: 27321946 Free PMC article.

4

Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance.

Blattner A, Huber AR, Röthlisberger B. Blattner A, et al. Am J Med Genet A. 2010 Aug;152A(8):2053-6. doi: 10.1002/ajmg.a.33504. Am J Med Genet A. 2010. PMID: 20635353

5

Wnt10b deficiency results in age-dependent loss of bone mass and progressive reduction of mesenchymal progenitor cells.

Stevens JR, Miranda-Carboni GA, Singer MA, Brugger SM, Lyons KM, Lane TF. Stevens JR, et al. J Bone Miner Res. 2010 Oct;25(10):2138-47. doi: 10.1002/jbmr.118. J Bone Miner Res. 2010. PMID: 20499361 Free PMC article.

6

Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation.

Ugur SA, Tolun A. Ugur SA, et al. Hum Mol Genet. 2008 Sep 1;17(17):2644-53. doi: 10.1093/hmg/ddn164. Epub 2008 May 30. Hum Mol Genet. 2008. PMID: 18515319

7

Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.

Elliott AM, Evans JA. Elliott AM, et al. Am J Med Genet A. 2006 Jul 1;140(13):1419-27. doi: 10.1002/ajmg.a.31244. Am J Med Genet A. 2006. PMID: 16688749

8

Evidence for autosomal recessive inheritance of split hand/split foot malformation: a report of nine cases.

Gül D, Oktenli C. Gül D, et al. Clin Dysmorphol. 2002 Jul;11(3):183-6. doi: 10.1097/00019605-200207000-00006. Clin Dysmorphol. 2002. PMID: 12072797

9

WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells.

Kirikoshi H, Sekihara H, Katoh M. Kirikoshi H, et al. Biochem Biophys Res Commun. 2001 May 18;283(4):798-805. doi: 10.1006/bbrc.2001.4855. Biochem Biophys Res Commun. 2001. PMID: 11350055

10

Inhibition of adipogenesis by Wnt signaling.

Ross SE, Hemati N, Longo KA, Bennett CN, Lucas PC, Erickson RL, MacDougald OA. Ross SE, et al. Science. 2000 Aug 11;289(5481):950-3. doi: 10.1126/science.289.5481.950. Science. 2000. PMID: 10937998

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

18 results

Results by year