Yu QC - Search Results

1

The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.

Cheng J, Syder AJ, Yu QC, Letai A, Paller AS, Fuchs E. Cheng J, et al. Among authors: yu qc. Cell. 1992 Sep 4;70(5):811-9. doi: 10.1016/0092-8674(92)90314-3. Cell. 1992. PMID: 1381287

2

Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity.

Syder AJ, Yu QC, Paller AS, Giudice G, Pearson R, Fuchs E. Syder AJ, et al. Among authors: yu qc. J Clin Invest. 1994 Apr;93(4):1533-42. doi: 10.1172/JCI117132. J Clin Invest. 1994. PMID: 7512983 Free PMC article.

3

Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex.

Chan YM, Yu QC, LeBlanc-Straceski J, Christiano A, Pulkkinen L, Kucherlapati RS, Uitto J, Fuchs E. Chan YM, et al. Among authors: yu qc. J Cell Sci. 1994 Apr;107 ( Pt 4):765-74. doi: 10.1242/jcs.107.4.765. J Cell Sci. 1994. PMID: 7520042

4

Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis.

Fuchs E, Coulombe P, Cheng J, Chan YM, Hutton E, Syder A, Degenstein L, Yu QC, Letai A, Vassar R. Fuchs E, et al. Among authors: yu qc. J Invest Dermatol. 1994 Nov;103(5 Suppl):25S-30S. doi: 10.1111/1523-1747.ep12398924. J Invest Dermatol. 1994. PMID: 7525738 Free article. Review.

5

Genetic and clinical mosaicism in a type of epidermal nevus.

Paller AS, Syder AJ, Chan YM, Yu QC, Hutton E, Tadini G, Fuchs E. Paller AS, et al. Among authors: yu qc. N Engl J Med. 1994 Nov 24;331(21):1408-15. doi: 10.1056/NEJM199411243312103. N Engl J Med. 1994. PMID: 7526210 Free article.

6

The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14.

Lloyd C, Yu QC, Cheng J, Turksen K, Degenstein L, Hutton E, Fuchs E. Lloyd C, et al. Among authors: yu qc. J Cell Biol. 1995 Jun;129(5):1329-44. doi: 10.1083/jcb.129.5.1329. J Cell Biol. 1995. PMID: 7539810 Free PMC article.

7

Disease severity correlates with position of keratin point mutations in patients with epidermolysis bullosa simplex.

Letai A, Coulombe PA, McCormick MB, Yu QC, Hutton E, Fuchs E. Letai A, et al. Among authors: yu qc. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3197-201. doi: 10.1073/pnas.90.8.3197. Proc Natl Acad Sci U S A. 1993. PMID: 7682695 Free PMC article.

8

The genetic basis of Weber-Cockayne epidermolysis bullosa simplex.

Chan YM, Yu QC, Fine JD, Fuchs E. Chan YM, et al. Among authors: yu qc. Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7414-8. doi: 10.1073/pnas.90.15.7414. Proc Natl Acad Sci U S A. 1993. PMID: 7688477 Free PMC article.

9

Ganglioside GT1b induces keratinocyte differentiation without activating protein kinase C.

Paller AS, Arnsmeier SL, Fisher GJ, Yu QC. Paller AS, et al. Among authors: yu qc. Exp Cell Res. 1995 Mar;217(1):118-24. doi: 10.1006/excr.1995.1070. Exp Cell Res. 1995. PMID: 7867710

10

Mice expressing a mutant desmosomal cadherin exhibit abnormalities in desmosomes, proliferation, and epidermal differentiation.

Allen E, Yu QC, Fuchs E. Allen E, et al. Among authors: yu qc. J Cell Biol. 1996 Jun;133(6):1367-82. doi: 10.1083/jcb.133.6.1367. J Cell Biol. 1996. PMID: 8682871 Free PMC article.

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