PubMed (GeneRIF) for id: 147409

Year	Number of Results
2003	2
2004	1
2005	1
2006	1
2007	2
2009	1
2011	1
2012	1
2014	1
2015	1
2018	1
2021	1
2022	1
2024	0

1

Autosomal recessive monilethrix: Novel variants of the DSG4 gene in three Chinese families.

Zhou C, Wang P, Yang D, Liao W, Guo Q, Li J, Wen G, Zheng S, Zhang X, Wang R, Zhang J. Zhou C, et al. Mol Genet Genomic Med. 2022 Apr;10(4):e1889. doi: 10.1002/mgg3.1889. Epub 2022 Feb 11. Mol Genet Genomic Med. 2022. PMID: 35146972 Free PMC article.

2

Desmoglein-4 Deficiency Exacerbates Psoriasiform Dermatitis in Rats While Psoriasis Patients Displayed a Decreased Gene Expression of DSG4.

Moreno-Sosa T, Sánchez MB, Pietrobon EO, Fernandez-Muñoz JM, Zoppino FCM, Neira FJ, Germanó MJ, Cargnelutti DE, Innocenti AC, Jahn GA, Valdez SR, Mackern-Oberti JP. Moreno-Sosa T, et al. Front Immunol. 2021 Apr 29;12:625617. doi: 10.3389/fimmu.2021.625617. eCollection 2021. Front Immunol. 2021. PMID: 33995349 Free PMC article.

3

Desmoglein 4 Mutation Underlies Autosomal Recessive Keratosis Pilaris Atrophicans.

Cohen-Barak E, Danial-Farran N, Hammad H, Aleme O, Krauz J, Gavish E, Khayat M, Ziv M, Shalev S. Cohen-Barak E, et al. Acta Derm Venereol. 2018 Aug 29;98(8):809-810. doi: 10.2340/00015555-2976. Acta Derm Venereol. 2018. PMID: 29796690 Free article. No abstract available.

4

A novel deletion mutation in the DSG4 gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families.

Ullah A, Raza SI, Ali RH, Naveed AK, Jan A, Rizvi SD, Satti R, Ahmad W. Ullah A, et al. Clin Exp Dermatol. 2015 Jan;40(1):78-84. doi: 10.1111/ced.12457. Epub 2014 Sep 23. Clin Exp Dermatol. 2015. PMID: 25251037

5

Desmoglein as a target in skin disease and beyond.

Amagai M, Stanley JR. Amagai M, et al. J Invest Dermatol. 2012 Mar;132(3 Pt 2):776-84. doi: 10.1038/jid.2011.390. Epub 2011 Dec 22. J Invest Dermatol. 2012. PMID: 22189787 Free PMC article. Review.

6

Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation.

Bazzi H, Demehri S, Potter CS, Barber AG, Awgulewitsch A, Kopan R, Christiano AM. Bazzi H, et al. Differentiation. 2009 Dec;78(5):292-300. doi: 10.1016/j.diff.2009.06.004. Epub 2009 Aug 15. Differentiation. 2009. PMID: 19683850 Free PMC article.

7

Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family.

Wajid M, Bazzi H, Rockey J, Lubetkin J, Zlotogorski A, Christiano AM. Wajid M, et al. J Invest Dermatol. 2007 Jul;127(7):1779-82. doi: 10.1038/sj.jid.5700791. Epub 2007 Mar 29. J Invest Dermatol. 2007. PMID: 17392831 Free article. No abstract available.

8

[Gene fragments cloned and immune recognition studied preliminarily for desmoglein 4 in pemphigus vulgaris].

Li W, Feng Y, Lu XY, Li JY, Ran YP. Li W, et al. Sichuan Da Xue Xue Bao Yi Xue Ban. 2007 Jan;38(1):84-7. Sichuan Da Xue Xue Bao Yi Xue Ban. 2007. PMID: 17294735 Chinese.

9

Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle.

Bazzi H, Getz A, Mahoney MG, Ishida-Yamamoto A, Langbein L, Wahl JK 3rd, Christiano AM. Bazzi H, et al. Differentiation. 2006 Mar;74(2-3):129-40. doi: 10.1111/j.1432-0436.2006.00061.x. Differentiation. 2006. PMID: 16533311

10

Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats.

Bazzi H, Martinez-Mir A, Kljuic A, Christiano AM. Bazzi H, et al. J Investig Dermatol Symp Proc. 2005 Dec;10(3):222-4. doi: 10.1111/j.1087-0024.2005.10110.x. J Investig Dermatol Symp Proc. 2005. PMID: 16382669 Free article.

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