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Results: 1-10 |
Results: 10
Unfolding retinal dystrophies: a role for molecular chaperones?
Authors: Chapple, JP Grayson, C Hardcastle, AJ Saliba, RS van der Spuy, J Cheetham, ME
Citation: Jp. Chapple et al., Unfolding retinal dystrophies: a role for molecular chaperones?, TRENDS MO M, 7(9), 2001, pp. 414-421
Sexually transmitted diseases during pregnancy: Screening, diagnostic, andtreatment practices among prenatal care providers in Georgia (vol 94, pg 47, 2001)
Authors: Weisbord, J Koumans, EH Toomey, KE Grayson, C Markowitz, LE
Citation: J. Weisbord et al., Sexually transmitted diseases during pregnancy: Screening, diagnostic, andtreatment practices among prenatal care providers in Georgia (vol 94, pg 47, 2001), SOUTH MED J, 94(3), 2001, pp. 303-303
Sexually transmitted diseases during pregnancy: Screening, diagnostic, andtreatment practices among prenatal care providers in Georgia
Authors: Weisbord, JS Koumans, EH Toomey, KE Grayson, C Markowitz, LE
Citation: Js. Weisbord et al., Sexually transmitted diseases during pregnancy: Screening, diagnostic, andtreatment practices among prenatal care providers in Georgia, SOUTH MED J, 94(1), 2001, pp. 47-53
Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane
Authors: Chapple, JP Hardcastle, AJ Grayson, C Spackman, LA Willison, KR Cheetham, ME
Citation: Jp. Chapple et al., Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane, HUM MOL GEN, 9(13), 2000, pp. 1919-1926
Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells
Authors: Grayson, C Reid, SNM Ellis, JA Rutherford, A Sowden, JC Yates, JRW Farber, DB Trump, D
Citation: C. Grayson et al., Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells, HUM MOL GEN, 9(12), 2000, pp. 1873-1879
A tribute to Foberto Ri
Authors: Grayson, C Roth, C
Citation: C. Grayson et C. Roth, A tribute to Foberto Ri, BELFAGOR, 55(5), 2000, pp. 526-526
Exclusion of RAI2 as the causative gene for Nance-Horan syndrome
Authors: Walpole, SM Ronce, N Grayson, C Dessay, B Yates, JRW Trump, D Toutain, A
Citation: Sm. Walpole et al., Exclusion of RAI2 as the causative gene for Nance-Horan syndrome, HUM GENET, 104(5), 1999, pp. 410-411
Explaining the gender difference in depressive symptoms
Authors: Nolen-Hoeksema, S Larson, J Grayson, C
Citation: S. Nolen-hoeksema et al., Explaining the gender difference in depressive symptoms, J PERS SOC, 77(5), 1999, pp. 1061-1072
Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegia
Authors: Reid, E Grayson, C Rubinsztein, DC Rogers, MT Rubinsztein, JS
Citation: E. Reid et al., Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegia, J MED GENET, 36(10), 1999, pp. 797-798
Locus-phenotype correlations in autosomal dominant pure hereditary spasticparaplegia - A clinical and molecular genetic study of 28 United Kingdom families
Authors: Reid, E Grayson, C Rogers, MT Rubinsztein, DC
Citation: E. Reid et al., Locus-phenotype correlations in autosomal dominant pure hereditary spasticparaplegia - A clinical and molecular genetic study of 28 United Kingdom families, BRAIN, 122, 1999, pp. 1741-1755
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