He Y - Search Results

1

Crucial role of posttranslational modifications of integrin α3 in interstitial lung disease and nephrotic syndrome.

Yalcin EG, He Y, Orhan D, Pazzagli C, Emiralioglu N, Has C. Yalcin EG, et al. Among authors: he y. Hum Mol Genet. 2015 Jul 1;24(13):3679-88. doi: 10.1093/hmg/ddv111. Epub 2015 Mar 25. Hum Mol Genet. 2015. PMID: 25810266

2

[Practical aspects of molecular diagnostics in genodermatoses].

Has C, He Y. Has C, et al. Among authors: he y. Hautarzt. 2016 Jan;67(1):53-8. doi: 10.1007/s00105-015-3721-y. Hautarzt. 2016. PMID: 26537890 Review. German.

3

Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity.

Pigors M, Kiritsi D, Krümpelmann S, Wagner N, He Y, Podda M, Kohlhase J, Hausser I, Bruckner-Tuderman L, Has C. Pigors M, et al. Among authors: he y. Hum Mol Genet. 2011 May 1;20(9):1811-9. doi: 10.1093/hmg/ddr064. Epub 2011 Feb 14. Hum Mol Genet. 2011. PMID: 21320868

4

Integrin α3 mutations with kidney, lung, and skin disease.

Has C, Spartà G, Kiritsi D, Weibel L, Moeller A, Vega-Warner V, Waters A, He Y, Anikster Y, Esser P, Straub BK, Hausser I, Bockenhauer D, Dekel B, Hildebrandt F, Bruckner-Tuderman L, Laube GF. Has C, et al. Among authors: he y. N Engl J Med. 2012 Apr 19;366(16):1508-14. doi: 10.1056/NEJMoa1110813. N Engl J Med. 2012. PMID: 22512483 Free PMC article.

5

Intronic ITGA3 Mutation Impacts Splicing Regulation and Causes Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa.

He Y, Balasubramanian M, Humphreys N, Waruiru C, Brauner M, Kohlhase J, O'Reilly R, Has C. He Y, et al. J Invest Dermatol. 2016 May;136(5):1056-1059. doi: 10.1016/j.jid.2015.11.031. Epub 2016 Feb 15. J Invest Dermatol. 2016. PMID: 26854491 Free article. Review. No abstract available.

6

Research Techniques Made Simple: Immunofluorescence Antigen Mapping in Epidermolysis Bullosa.

Has C, He Y. Has C, et al. Among authors: he y. J Invest Dermatol. 2016 Jul;136(7):e65-e71. doi: 10.1016/j.jid.2016.05.093. J Invest Dermatol. 2016. PMID: 27342035 Free article.

7

UV-B-induced cutaneous inflammation and prospects for antioxidant treatment in Kindler syndrome.

Maier K, He Y, Wölfle U, Esser PR, Brummer T, Schempp C, Bruckner-Tuderman L, Has C. Maier K, et al. Among authors: he y. Hum Mol Genet. 2016 Dec 15;25(24):5339-5352. doi: 10.1093/hmg/ddw350. Hum Mol Genet. 2016. PMID: 27798104

8

Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility.

He Y, Maier K, Leppert J, Hausser I, Schwieger-Briel A, Weibel L, Theiler M, Kiritsi D, Busch H, Boerries M, Hannula-Jouppi K, Heikkilä H, Tasanen K, Castiglia D, Zambruno G, Has C. He Y, et al. Am J Hum Genet. 2016 Dec 1;99(6):1395-1404. doi: 10.1016/j.ajhg.2016.11.005. Epub 2016 Nov 23. Am J Hum Genet. 2016. PMID: 27889062 Free PMC article.

9

Absence of the Integrin α3 Subunit Induces an Activated Phenotype in Human Keratinocytes.

Pazzagli C, He Y, Busch H, Esser P, Kiritsi D, Gache Y, Bruckner-Tuderman L, Boerries M, Has C. Pazzagli C, et al. Among authors: he y. J Invest Dermatol. 2017 Jun;137(6):1387-1391. doi: 10.1016/j.jid.2017.01.018. Epub 2017 Feb 3. J Invest Dermatol. 2017. PMID: 28163067 Free article. No abstract available.

10

Renal-skin syndromes.

Has C, He Y. Has C, et al. Among authors: he y. Cell Tissue Res. 2017 Jul;369(1):63-73. doi: 10.1007/s00441-017-2623-y. Epub 2017 Apr 22. Cell Tissue Res. 2017. PMID: 28432467 Review.

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