PubMed for id: 50814

Year	Number of Results
1992	1
1993	2
1996	2
2000	4
2002	2
2003	3
2004	3
2005	2
2006	1
2007	2
2008	3
2009	3
2010	4
2011	4
2012	2
2014	1
2015	7
2016	2
2017	5
2018	10
2019	9
2020	13
2021	14
2022	13
2023	6
2024	2

1

NSDHL promotes triple-negative breast cancer metastasis through the TGFβ signaling pathway and cholesterol biosynthesis.

Chen M, Zhao Y, Yang X, Zhao Y, Liu Q, Liu Y, Hou Y, Sun H, Jin W. Chen M, et al. Breast Cancer Res Treat. 2021 Jun;187(2):349-362. doi: 10.1007/s10549-021-06213-8. Epub 2021 Apr 16. Breast Cancer Res Treat. 2021. PMID: 33864166

2

CHILD syndrome in a Malaysian adult with identification of a novel heterozygous missense mutation NSDHL c.602A>G.

Tang MM, Tan WC, Surana U, Leong KF, Pramano ZAD. Tang MM, et al. Int J Dermatol. 2021 Apr;60(4):e154-e156. doi: 10.1111/ijd.15296. Epub 2020 Nov 10. Int J Dermatol. 2021. PMID: 33169834 No abstract available.

3

NAD(P)-dependent steroid dehydrogenase-like is involved in breast cancer cell growth and metastasis.

Yoon SH, Kim HS, Kim RN, Jung SY, Hong BS, Kang EJ, Lee HB, Moon HG, Noh DY, Han W. Yoon SH, et al. BMC Cancer. 2020 May 4;20(1):375. doi: 10.1186/s12885-020-06840-2. BMC Cancer. 2020. PMID: 32366230 Free PMC article.

4

Crystal structures of human NSDHL and development of its novel inhibitor with the potential to suppress EGFR activity.

Kim DG, Cho S, Lee KY, Cheon SH, Yoon HJ, Lee JY, Kim D, Shin KS, Koh CH, Koo JS, Choi Y, Lee HH, Oh YK, Jeong YS, Chung SJ, Baek M, Jung KY, Lim HJ, Kim HS, Park SJ, Lee JY, Lee SJ, Lee BJ. Kim DG, et al. Cell Mol Life Sci. 2021 Jan;78(1):207-225. doi: 10.1007/s00018-020-03490-2. Epub 2020 Mar 5. Cell Mol Life Sci. 2021. PMID: 32140747

5

Identification of NSDHL mutations associated with CHILD syndrome in oral verruciform xanthoma.

Getz GI, Parag-Sharma K, Reside J, Padilla RJ, Amelio AL. Getz GI, et al. Oral Surg Oral Med Oral Pathol Oral Radiol. 2019 Jul;128(1):60-69. doi: 10.1016/j.oooo.2019.02.015. Epub 2019 Feb 23. Oral Surg Oral Med Oral Pathol Oral Radiol. 2019. PMID: 31078502

6

NSDHL-containing duplication at Xq28 in a male patient with autism spectrum disorder: a case report.

Hu CC, Sun YJ, Liu CX, Zhou BR, Li CY, Xu Q, Xu X. Hu CC, et al. BMC Med Genet. 2018 Oct 30;19(1):192. doi: 10.1186/s12881-018-0705-7. BMC Med Genet. 2018. PMID: 30376821 Free PMC article.

7

CHILD Syndrome: Case Report of a Chinese Patient and Literature Review of the NAD[P]H Steroid Dehydrogenase-Like Protein Gene Mutation.

Mi XB, Luo MX, Guo LL, Zhang TD, Qiu XW. Mi XB, et al. Pediatr Dermatol. 2015 Nov-Dec;32(6):e277-82. doi: 10.1111/pde.12701. Epub 2015 Oct 13. Pediatr Dermatol. 2015. PMID: 26459993 Review.

8

Large deletions in the NSDHL gene in two patients with CHILD syndrome.

Yang Z, Hartmann B, Xu Z, Ma L, Happle R, Schlipf N, Zhang LX, Xu ZG, Wang ZY, Fischer J. Yang Z, et al. Acta Derm Venereol. 2015 Nov;95(8):1007-8. doi: 10.2340/00015555-2143. Acta Derm Venereol. 2015. PMID: 26014843 Free article. No abstract available.

9

A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next-generation sequencing causes CK syndrome.

Preiksaitiene E, Caro A, Benušienė E, Oltra S, Orellana C, Morkūnienė A, Roselló MP, Kasnauskiene J, Monfort S, Kučinskas V, Mayo S, Martinez F. Preiksaitiene E, et al. Am J Med Genet A. 2015 Jun;167(6):1342-8. doi: 10.1002/ajmg.a.36999. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25900314

10

Expression profile of NSDHL in human peripheral tissues.

Morimoto M, Souich Cd, Trinh J, McLarren KW, Boerkoel CF, Hendson G. Morimoto M, et al. J Mol Histol. 2012 Feb;43(1):95-106. doi: 10.1007/s10735-011-9375-x. Epub 2011 Nov 24. J Mol Histol. 2012. PMID: 22113624

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