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1.

Accelerated Skeletal Maturation in Disorders of Retinoic Acid Metabolism: A Case Report and Focused Review of the Literature.

Nilsson, O; Isoherranen, N; Guo, M H; Lui, J C; Jee, Y H; Guttmann-Bauman, I; Acerini, C; Lee, W; Allikmets, R; Yanovski, J A; Dauber, A; Baron, J.

Horm Metab Res ; 48(11): 737-744, 2016 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-27589347

2.

Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption.

Lee, M H; Lu, K; Hazard, S; Yu, H; Shulenin, S; Hidaka, H; Kojima, H; Allikmets, R; Sakuma, N; Pegoraro, R; Srivastava, A K; Salen, G; Dean, M; Patel, S B.

Nat Genet ; 27(1): 79-83, 2001 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-11138003

3.

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.

Allikmets, R; Singh, N; Sun, H; Shroyer, N F; Hutchinson, A; Chidambaram, A; Gerrard, B; Baird, L; Stauffer, D; Peiffer, A; Rattner, A; Smallwood, P; Li, Y; Anderson, K L; Lewis, R A; Nathans, J; Leppert, M; Dean, M; Lupski, J R.

Nat Genet ; 15(3): 236-46, 1997 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-9054934

4.

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.

Nat Genet ; 27(1): 89-93, 2001 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-11138005

5.

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.

Schmidt, L; Duh, F M; Chen, F; Kishida, T; Glenn, G; Choyke, P; Scherer, S W; Zhuang, Z; Lubensky, I; Dean, M; Allikmets, R; Chidambaram, A; Bergerheim, U R; Feltis, J T; Casadevall, C; Zamarron, A; Bernues, M; Richard, S; Lips, C J; Walther, M M; Tsui, L C; Geil, L; Orcutt, M L; Stackhouse, T; Lipan, J; Slife, L; Brauch, H; Decker, J; Niehans, G; Hughson, M D; Moch, H; Storkel, S; Lerman, M I; Linehan, W M; Zbar, B.

Nat Genet ; 16(1): 68-73, 1997 May.

Artículo en Inglés | MEDLINE | ID: mdl-9140397

6.

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.

Allikmets, R; Shroyer, N F; Singh, N; Seddon, J M; Lewis, R A; Bernstein, P S; Peiffer, A; Zabriskie, N A; Li, Y; Hutchinson, A; Dean, M; Lupski, J R; Leppert, M.

Science ; 277(5333): 1805-7, 1997 Sep 19.

Artículo en Inglés | MEDLINE | ID: mdl-9295268

7.

Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study.

Dean, M; Carrington, M; Winkler, C; Huttley, G A; Smith, M W; Allikmets, R; Goedert, J J; Buchbinder, S P; Vittinghoff, E; Gomperts, E; Donfield, S; Vlahov, D; Kaslow, R; Saah, A; Rinaldo, C; Detels, R; O'Brien, S J.

Science ; 273(5283): 1856-62, 1996 Sep 27.

Artículo en Inglés | MEDLINE | ID: mdl-8791590

8.

Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy.

Kong, J; Kim, S-R; Binley, K; Pata, I; Doi, K; Mannik, J; Zernant-Rajang, J; Kan, O; Iqball, S; Naylor, S; Sparrow, J R; Gouras, P; Allikmets, R.

Gene Ther ; 15(19): 1311-20, 2008 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-18463687

9.

Evolution of ATP-binding cassette transporter genes.

Dean, M; Allikmets, R.

Curr Opin Genet Dev ; 5(6): 779-85, 1995 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-8745077

10.

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.

Allikmets, R.

Nat Genet ; 17(1): 122, 1997 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-9288113

11.

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR.

Martínez-Mir, A; Paloma, E; Allikmets, R; Ayuso, C; del Rio, T; Dean, M; Vilageliu, L; Gonzàlez-Duarte, R; Balcells, S.

Nat Genet ; 18(1): 11-2, 1998 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-9425888

12.

A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance.

Allikmets, R; Schriml, L M; Hutchinson, A; Romano-Spica, V; Dean, M.

Cancer Res ; 58(23): 5337-9, 1998 Dec 01.

Artículo en Inglés | MEDLINE | ID: mdl-9850061

13.

The gene from the short arm of chromosome 3, at D3F15S2, frequently deleted in renal cell carcinoma, encodes acylpeptide hydrolase.

Erlandsson, R; Boldog, F; Persson, B; Zabarovsky, E R; Allikmets, R L; Sümegi, J; Klein, G; Jörnvall, H.

Oncogene ; 6(7): 1293-5, 1991 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-1861871

14.

Identification of P-glycoprotein/multidrug resistance genes from model organisms.

Allikmets, R; Gerrard, B; Stewart, C; White, M; Dean, M.

Leukemia ; 7 Suppl 2: S13-7, 1993 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-8361216

15.

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.

Jaakson, K; Zernant, J; Külm, M; Hutchinson, A; Tonisson, N; Glavac, D; Ravnik-Glavac, M; Hawlina, M; Meltzer, M R; Caruso, R C; Testa, F; Maugeri, A; Hoyng, C B; Gouras, P; Simonelli, F; Lewis, R A; Lupski, J R; Cremers, F P M; Allikmets, R.

Hum Mutat ; 22(5): 395-403, 2003 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-14517951

16.

An improved technique for the efficient construction of gene libraries by partial filling-in of cohesive ends.

Zabarovsky, E R; Allikmets, R L.

Gene ; 42(1): 119-23, 1986.

Artículo en Inglés | MEDLINE | ID: mdl-3013727

17.

Cloning and organization of the abc and mdl genes of Escherichia coli: relationship to eukaryotic multidrug resistance.

Allikmets, R; Gerrard, B; Court, D; Dean, M.

Gene ; 136(1-2): 231-6, 1993 Dec 22.

Artículo en Inglés | MEDLINE | ID: mdl-7904973

18.

Regulatory elements and transcriptional regulation by testosterone and retinoic acid of the rat nerve growth factor receptor promoter.

Metsis, M; Timmusk, T; Allikmets, R; Saarma, M; Persson, H.

Gene ; 121(2): 247-54, 1992 Nov 16.

Artículo en Inglés | MEDLINE | ID: mdl-1446821

19.

Organization of the ABCR gene: analysis of promoter and splice junction sequences.

Allikmets, R; Wasserman, W W; Hutchinson, A; Smallwood, P; Nathans, J; Rogan, P K; Schneider, T D; Dean, M.

Gene ; 215(1): 111-22, 1998 Jul 17.

Artículo en Inglés | MEDLINE | ID: mdl-9666097

20.

Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12.

Tammur, J; Prades, C; Arnould, I; Rzhetsky, A; Hutchinson, A; Adachi, M; Schuetz, J D; Swoboda, K J; Ptácek, L J; Rosier, M; Dean, M; Allikmets, R.

Gene ; 273(1): 89-96, 2001 Jul 25.

Artículo en Inglés | MEDLINE | ID: mdl-11483364

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Accelerated Skeletal Maturation in Disorders of Retinoic Acid Metabolism: A Case Report and Focused Review of the Literature.

Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption.

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.

Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.

Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study.

Correction of the disease phenotype in the mouse model of Stargardt disease by lentiviral gene therapy.

Evolution of ATP-binding cassette transporter genes.

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR.

A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance.

The gene from the short arm of chromosome 3, at D3F15S2, frequently deleted in renal cell carcinoma, encodes acylpeptide hydrolase.

Identification of P-glycoprotein/multidrug resistance genes from model organisms.

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.

An improved technique for the efficient construction of gene libraries by partial filling-in of cohesive ends.

Cloning and organization of the abc and mdl genes of Escherichia coli: relationship to eukaryotic multidrug resistance.

Regulatory elements and transcriptional regulation by testosterone and retinoic acid of the rat nerve growth factor receptor promoter.

Organization of the ABCR gene: analysis of promoter and splice junction sequences.

Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12.