Ho L - Search Results

1

Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA).

Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH Jr. Morell R, et al. Among authors: ho l. Hum Mol Genet. 1997 May;6(5):659-64. doi: 10.1093/hmg/6.5.659. Hum Mol Genet. 1997. PMID: 9158138

2

A gene for autosomal dominant hypohidrotic ectodermal dysplasia (EDA3) maps to chromosome 2q11-q13.

Ho L, Williams MS, Spritz RA. Ho L, et al. Am J Hum Genet. 1998 May;62(5):1102-6. doi: 10.1086/301839. Am J Hum Genet. 1998. PMID: 9545409 Free PMC article.

3

Mutational analysis of copper binding by human tyrosinase.

Spritz RA, Ho L, Furumura M, Hearing VJ Jr. Spritz RA, et al. Among authors: ho l. J Invest Dermatol. 1997 Aug;109(2):207-12. doi: 10.1111/1523-1747.ep12319351. J Invest Dermatol. 1997. PMID: 9242509 Free article.

4

Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1).

Spritz RA, Oh J, Fukai K, Holmes SA, Ho L, Chitayat D, France TD, Musarella MA, Orlow SJ, Schnur RE, Weleber RG, Levin AV. Spritz RA, et al. Among authors: ho l. Hum Mutat. 1997;10(2):171-4. doi: 10.1002/(SICI)1098-1004(1997)10:2<171::AID-HUMU11>3.0.CO;2-X. Hum Mutat. 1997. PMID: 9259202 No abstract available.

5

Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity.

Oh J, Ho L, Ala-Mello S, Amato D, Armstrong L, Bellucci S, Carakushansky G, Ellis JP, Fong CT, Green JS, Heon E, Legius E, Levin AV, Nieuwenhuis HK, Pinckers A, Tamura N, Whiteford ML, Yamasaki H, Spritz RA. Oh J, et al. Among authors: ho l. Am J Hum Genet. 1998 Mar;62(3):593-8. doi: 10.1086/301757. Am J Hum Genet. 1998. PMID: 9497254 Free PMC article.

6

Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles.

Oh J, Bailin T, Fukai K, Feng GH, Ho L, Mao JI, Frenk E, Tamura N, Spritz RA. Oh J, et al. Among authors: ho l. Nat Genet. 1996 Nov;14(3):300-6. doi: 10.1038/ng1196-300. Nat Genet. 1996. PMID: 8896559

7

Inhibition of proliferation of human melanocytes by a KIT antisense oligodeoxynucleotide: implications for human piebaldism and mouse dominant white spotting (W).

Spritz RA, Ho L, Strunk KM. Spritz RA, et al. Among authors: ho l. J Invest Dermatol. 1994 Aug;103(2):148-50. doi: 10.1111/1523-1747.ep12392551. J Invest Dermatol. 1994. PMID: 7518854 Free article.

8

Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences.

Sviderskaya EV, Bennett DC, Ho L, Bailin T, Lee ST, Spritz RA. Sviderskaya EV, et al. Among authors: ho l. J Invest Dermatol. 1997 Jan;108(1):30-4. doi: 10.1111/1523-1747.ep12285621. J Invest Dermatol. 1997. PMID: 8980282 Free article.

9

Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism.

Ezoe K, Holmes SA, Ho L, Bennett CP, Bolognia JL, Brueton L, Burn J, Falabella R, Gatto EM, Ishii N, et al. Ezoe K, et al. Among authors: ho l. Am J Hum Genet. 1995 Jan;56(1):58-66. Am J Hum Genet. 1995. PMID: 7529964 Free PMC article.

10

Role of Metformin in Preventing New-Onset Chronic Kidney Disease in Patients with Type 2 Diabetes Mellitus.

Lin YL, Lin SH, Wang HH, Hsu WC, Hung SY, Chiou YY, Liou HH, Chang MY, Ho LC, Wu CF, Lee YC. Lin YL, et al. Among authors: ho lc. Pharmaceuticals (Basel). 2025 Jan 14;18(1):95. doi: 10.3390/ph18010095. Pharmaceuticals (Basel). 2025. PMID: 39861157 Free article.

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