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Results: 1-10 |
Results: 10
Disease model: heritable skin blistering
Authors: Arin, MJ Roop, DR
Citation: Mj. Arin et Dr. Roop, Disease model: heritable skin blistering, TRENDS MO M, 7(9), 2001, pp. 422-424
Gene therapy for inherited skin diseases
Authors: Cao, TY Arin, MJ Roop, DR
Citation: Ty. Cao et al., Gene therapy for inherited skin diseases, CURR P D-US, 13(3), 2001, pp. 173-182
Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders
Authors: Arin, MJ Longley, MA Wang, XJ Roop, DR
Citation: Mj. Arin et al., Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders, J CELL BIOL, 152(3), 2001, pp. 645-649
Relevant animal models for skin gene therapy
Authors: Arin, MJ Cao, T Berton, TR Zhou, Z Wang, XJ Roop, DR
Citation: Mj. Arin et al., Relevant animal models for skin gene therapy, SKIN AND GENE THERAPY, 2001, pp. 35-51
Hot spot mutations in keratin 2e suggest a correlation between genotype and phenotype in patients with ichthyosis bullosa of Siemens
Authors: Suga, Y Arin, MJ Scott, G Goldsmith, LA Magro, CM Baden, LA Baden, HP Roop, DR
Citation: Y. Suga et al., Hot spot mutations in keratin 2e suggest a correlation between genotype and phenotype in patients with ichthyosis bullosa of Siemens, EXP DERMATO, 9(1), 2000, pp. 11-15
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis
Authors: Arin, MJ Longley, MA Epstein, EH Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis, EXP DERMATO, 9(1), 2000, pp. 16-19
Ion-pair reversed-phase HPLC determination of creatinine in urine
Authors: Resines, JA Arin, MJ Diez, MT del Moral, PG
Citation: Ja. Resines et al., Ion-pair reversed-phase HPLC determination of creatinine in urine, J LIQ CHR R, 22(16), 1999, pp. 2503-2510
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis
Authors: Arin, MJ Longley, MA Kuster, W Huber, M Hohl, D Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis, EXP DERMATO, 8(2), 1999, pp. 124-127
A novel substitution in keratin 10 in epidermolytic hyperkeratosis
Authors: Arin, MJ Longley, MA Anton-Lamprech, I Kurze, G Huber, M Hohl, D Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., A novel substitution in keratin 10 in epidermolytic hyperkeratosis, J INVES DER, 112(4), 1999, pp. 506-508
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens
Authors: Arin, MJ Longley, MA Epstein, EH Scott, G Goldsmith, LA Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens, J INVES DER, 112(3), 1999, pp. 380-382
Risultati: 1-10 |