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Publications by White, K

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Jump to: 2002 | 2001 | 2000 | 1999
Number of items: 16.

2002

Weber, Bernhard H. F. , Lin, B, White, K, Kohler, K, Soboleva, G, Herterich, S, Seeliger, M W, Jaissle, G B, Grimm, C, Reme, C, Wenzel, A, Asan, E and Schrewe, H (2002) A mouse model for Sorsby fundus dystrophy. Investigative ophthalmology and visual science 43 (8), pp. 2732-2740.

Schulz, H L, Stöhr, H, White, K, van Driel, M A, Hoyng, C B, Cremers, F and Weber, Bernhard H. F. (2002) Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy. Molecular vision 8, pp. 67-71.

2001

White, K, Held, K R and Weber, Bernhard H. F. (2001) A BRCA2 germ-line mutation in familial pancreatic carcinoma. International Journal of Cancer 91 (5), pp. 742-744. Fulltext not available.

Sauer, C G, White, K, Kellner, U, Rudolph, G, Jurklies, B, Pauleikhoff, D and Weber, Bernhard H. F. (2001) EFEMP1 is not associated with sporadic early onset drusen. Ophthalmic Genetics 22, pp. 27-34. Fulltext not available.

Oldenburg, J, Ivaskevicius, V, Rost, S, Fregin, A, White, K, Holinski-Feder, E, Müller-Reible, C R and Weber, Bernhard H. F. (2001) Evaluation of DHPLC in the analysis of hemophilia A. Journal of Biochemical and Biophysical Methods 47 (1-2), pp. 39-51. Fulltext not available.

Sauer, C G, White, K, Stöhr, H, Grimm, T, Hutchinson, A, Bernstein, P S, Lewis, R A, Simonelli, F, Pauleikhoff, D, Allikmets, R and Weber, Bernhard H. F. (2001) Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration. British Journal of Ophthalmology 85 (8), pp. 969-975. Fulltext not available.

Mah, N, Stöhr, H, Schulz, H L, White, K and Weber, Bernhard H. F. (2001) Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes. Biochimica et Biophysica Acta - Gene Structure and Expression 1522 (3), pp. 167-174. Fulltext not available.

Scholl, H P N, Kremers, J, Vonthein, R, White, K and Weber, Bernhard H. F. (2001) L- and M-Cone–Driven Electroretinograms in Stargardt’s Macular Dystrophy–Fundus Flavimaculatus. Investigative ophthalmology and visual science 42, pp. 1380-1389.

2000

Krämer, F, White, K, Kubbies, M, Swisshelm, K and Weber, Bernhard H. F. (2000) Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancer. Human Genetics 107 (3), pp. 249-256. Fulltext not available.

Rivera, A, White, K, Stöhr, H, Steiner, K, Hemmrich, N, Grimm, T, Jurklies, B, Lorenz, B, Scholl, H P N, Apfelstedt-Sylla, E and Weber, Bernhard H. F. (2000) A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration. The American Journal of Human Genetics 67 (4), pp. 800-813. Fulltext not available.

Krämer, F, White, K, Pauleikhoff, D, Gehrig, A, Passmore, L, Rivera, A, Rudolph, G, Kellner, U, Andrassi, M, Lorenz, B, Rohrschneider, K, Blankenagel, A, Jurklies, B, Schilling, H, Schütt, F, Holz, F G and Weber, Bernhard H. F. (2000) Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. European Journal of Human Genetics 8 (4), pp. 286-292. Fulltext not available.

Hofferbert, S, Worringen, U, Backe, J, Rückert, E-M, White, K, Faller, H, Grimm, T, Caffier, H, Chang-Claude, J and Weber, Bernhard H. F. (2000) Simultaneous Interdisciplinary counseling in germany breast/ovarian cancer families: first experiences with patient perceptions, surveillance behavior and acceptance of genetic testing. Genetic Counseling 11, pp. 127-146. Fulltext not available.

White, K, Marquardt, A and Weber, Bernhard H. F. (2000) VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies. Human Mutation 15 (4), pp. 301-308. Fulltext not available.

Marquardt, A, Stöhr, H, White, K and Weber, Bernhard H. F. (2000) cDNA Cloning, Genomic Structure, and Chromosomal Localization of Three Members of the Human Fatty Acid Desaturase Family. Genomics 66 (2), pp. 175-183. Fulltext not available.

Stöhr, H, Marquardt, A, White, K and Weber, Bernhard H. F. (2000) cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12→q13.1 which encodes a highly conserved, potential membrane-associated protein. Cytogenetics and cell genetics 88, pp. 211-216. Fulltext not available.

1999

Gehrig, A E, White, K, Lorenz, B, Adrassi, M, Clemens, S and Weber, Bernhard H. F. (1999) Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis. Clinical Genetics 55 (6), pp. 461-465. Fulltext not available.

This list was generated on Sun Aug 9 05:45:49 2020 CEST.
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