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Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
closedAccess | | 29-ago-2012 | A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q | Kamenarova, Kunka; Romero-Durán, Margarita CSIC; Valdés-Sánchez, María Lourdes; Bhattacharya, Shom Shanker CSIC ORCID; Chakarova, Christina | artículo |
openAccess | | mar-2000 | A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13 | Hameed, Abdul; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
openAccess | | jul-2006 | A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family | Addison, Peter K. F.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
closedAccess | | mar-2006 | A study of the nuclear trafficking of the splicing factor protein PRPF31 linked to autosomal dominant retinitis pigmentosa (ADRP) | Wilkie, Susan E.; Bhattacharya, Shom Shanker CSIC ORCID; Hunt, David M. | artículo |
closedAccess | | 1994 | A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28 | Curtis, A. R.; Lindsay, S.; Boye, E.; Clarke, A. J.; Landy, S. J.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
closedAccess | | ago-1995 | A YAC Contig Spanning the Dominant Retinitis Pigmentosa Locus (RP9) on Chromosome 7p | Keen, T. Jeffrey; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
openAccess | | 1992 | Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation | Moore, Anthony T.; Fitzke, Fred W.; Kemp, Colin M.; Arden, Geoffrey B.; Keen, T. Jeffrey; Inglehearn, Christopher F.; Bhattacharya, Shom Shanker CSIC ORCID; Bird, Alan C. | artículo |
closedAccess | | dic-2000 | Abnormalities of the transforming growth factor-beta pathway in ocular melanoma | Myatt, Nyree; Bhattacharya, Shom Shanker CSIC ORCID; Cree, Ian A. | artículo |
openAccess | | feb-1993 | Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani family | Curtis, Ann; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
closedAccess | | 1998 | Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse | Ali, Robin R.; Reichel, Martin B.; Kanuga, Naheed; Munro, Peter M.; Alexander, Robert A.; Clarke, Alan R.; Luthert, Philip J.; Bhattacharya, Shom Shanker CSIC ORCID; Hunt, David M. | artículo |
closedAccess | | 24-nov-1979 | Actual or standard bicarbonate? | Tibi, Laila; Bhattacharya, Shom Shanker CSIC ORCID; Flear, Cecil T. G. | carta al director |
openAccess | | mar-2008 | Adeno-Associated Virus Gene Transfer to Mouse Retina | Ali, Robin R.; Bhattacharya, Shom Shanker CSIC ORCID; Thrasher, Adrián J. | artículo |
closedAccess | | 2001 | Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans | Berry, Vanita; Bhattacharya, Shom Shanker CSIC ORCID; Quinlan, Roy A. | artículo |
openAccess | | ene-2000 | An Analysis of ABCR Mutations in British Patients with Recessive Retinal Dystrophies | Papaioannou, Myrto G.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
openAccess | | dic-2007 | An Assessment of the Apex Microarray Technology in Genotyping Patients with Leber Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy | Henderson, Robert H.; Bhattacharya, Shom Shanker CSIC ORCID; Moore, Anthony T. | artículo |
closedAccess | | 1-ago-1995 | An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q | Bardien, Soraya; Ebenezer, Neil D.; Greenberg, Jacquie; Inglehearn, Christopher F.; Bartmann, Lecia; Goliath, Rene; Beighton, Peter; Ramesar, Rajkumar; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
openAccess | | 2001 | An immune response after intraocular administration of an adenoviral vector containing a β galactosidase reporter gene slows retinal degeneration in the rd mouse | Reichel, Martin B.; Bhattacharya, Shom Shanker CSIC ORCID; Ali, Robin R. | artículo |
closedAccess | | abr-2002 | An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders | Thiselton, Dawn L.; Bhattacharya, Shom Shanker CSIC ORCID; Meindl, Alfons | artículo |
closedAccess | | 1-mar-1998 | Anterior polar cataract: clinical spectrum and genetic linkage in a single family | Ionides, Alexander; Berry, Vanita; Mackay, Donna; Shiels, Alan; Bhattacharya, Shom Shanker CSIC ORCID; Moore, Anthony T. | artículo |
closedAccess | | 2001 | Assignment (1) of BCL2L11 to human chromosome band 2p13 with somatic cell and radiation hybrids | Murray, S.; Halford, S.; Ebenezer, Neil D.; Gregory-Evans, Cheryl Y.; Bhattacharya, Shom Shanker CSIC ORCID | artículo |