K08-AR02141/AR/NIAMS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2001	2
2002	1
2003	5
2004	4
2005	3
2006	3
2007	2
2008	1
2025	0

1

Richard G. Richard G. Clin Dermatol. 2005 Jan-Feb;23(1):23-32. doi: 10.1016/j.clindermatol.2004.09.010. Clin Dermatol. 2005. PMID: 15708286 Review.

2

Connexin disorders of the skin.

Richard G. Richard G. Adv Dermatol. 2001;17:243-77. Adv Dermatol. 2001. PMID: 11758118 Review. No abstract available.

3

KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

Lugassy J, McGrath JA, Itin P, Shemer R, Verbov J, Murphy HR, Ishida-Yamamoto A, Digiovanna JJ, Bercovich D, Karin N, Vitenshtein A, Uitto J, Bergman R, Richard G, Sprecher E. Lugassy J, et al. J Invest Dermatol. 2008 Jun;128(6):1517-24. doi: 10.1038/sj.jid.5701187. Epub 2007 Nov 29. J Invest Dermatol. 2008. PMID: 18049449 Free article.

4

Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5.

Sprecher E, Yosipovitch G, Bergman R, Ciubutaro D, Indelman M, Pfendner E, Goh LC, Miller CJ, Uitto J, Richard G. Sprecher E, et al. J Invest Dermatol. 2003 Apr;120(4):623-6. doi: 10.1046/j.1523-1747.2003.12084.x. J Invest Dermatol. 2003. PMID: 12648226 Free article.

5

Malignant proliferating pilar tumors arising in KID syndrome: a report of two patients.

Nyquist GG, Mumm C, Grau R, Crowson AN, Shurman DL, Benedetto P, Allen P, Lovelace K, Smith DW, Frieden I, Hybarger CP, Richard G. Nyquist GG, et al. Am J Med Genet A. 2007 Apr 1;143A(7):734-41. doi: 10.1002/ajmg.a.31635. Am J Med Genet A. 2007. PMID: 17330861

6

Molecular genetics of the ichthyoses.

Richard G. Richard G. Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):32-44. doi: 10.1002/ajmg.c.30032. Am J Med Genet C Semin Med Genet. 2004. PMID: 15452860 Review.

7

In vivo studies of mutant keratin 1 in ichthyosis hystrix Curth-Macklin.

Ishida-Yamamoto A, Richard G, Takahashi H, Iizuka H. Ishida-Yamamoto A, et al. J Invest Dermatol. 2003 Mar;120(3):498-500. doi: 10.1046/j.1523-1747.2003.12064.x. J Invest Dermatol. 2003. PMID: 12603866 Free article. No abstract available.

8

A novel GJB2 (connexin 26) mutation, F142L, in a patient with unusual mucocutaneous findings and deafness.

Brown CW, Levy ML, Flaitz CM, Reid BS, Manolidis S, Hebert AA, Bender MM, Heilstedt HA, Plunkett KS, Fang P, Roa BB, Chung P, Tang HY, Richard G, Alford RL. Brown CW, et al. J Invest Dermatol. 2003 Nov;121(5):1221-3. doi: 10.1046/j.1523-1747.2003.12550_4.x. J Invest Dermatol. 2003. PMID: 14708631 Free article. No abstract available.

9

Epidermolysis Bullosa Simplex with mottled pigmentation: mutation analysis in the first reported Hispanic pedigree with the largest single generation of affected individuals to date.

Shurman D, Losi-Sasaki J, Grimwood R, Kivirikko S, Tichy E, Uitto J, Richard G. Shurman D, et al. Eur J Dermatol. 2006 Mar-Apr;16(2):132-5. Eur J Dermatol. 2006. PMID: 16581562

10

In vivo and in vitro expression of connexins in the human corneal epithelium.

Shurman DL, Glazewski L, Gumpert A, Zieske JD, Richard G. Shurman DL, et al. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):1957-65. doi: 10.1167/iovs.04-1364. Invest Ophthalmol Vis Sci. 2005. PMID: 15914609

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