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The P30 movement protein of tobacco mosaic virus is a single-strand nucleic acid binding protein.
Citovsky V, Knorr D, Schuster G, Zambryski P. Citovsky V, et al. Among authors: knorr d. Cell. 1990 Feb 23;60(4):637-47. doi: 10.1016/0092-8674(90)90667-4. Cell. 1990. PMID: 2302736
cDNA cloning of the complete genome of tobacco mosaic virus and production of infectious transcripts.
Dawson WO, Beck DL, Knorr DA, Grantham GL. Dawson WO, et al. Among authors: knorr da. Proc Natl Acad Sci U S A. 1986 Mar;83(6):1832-6. doi: 10.1073/pnas.83.6.1832. Proc Natl Acad Sci U S A. 1986. PMID: 16593669 Free PMC article.
A point mutation in the tobacco mosaic virus capsid protein gene induces hypersensitivity in Nicotiana sylvestris.
Knorr DA, Dawson WO. Knorr DA, et al. Proc Natl Acad Sci U S A. 1988 Jan;85(1):170-4. doi: 10.1073/pnas.85.1.170. Proc Natl Acad Sci U S A. 1988. PMID: 16578827 Free PMC article.
De novo generation of defective interfering RNAs of tomato bushy stunt virus by high multiplicity passage.
Knorr DA, Mullin RH, Hearne PQ, Morris TJ. Knorr DA, et al. Virology. 1991 Mar;181(1):193-202. doi: 10.1016/0042-6822(91)90484-s. Virology. 1991. PMID: 1994574 Free PMC article.
The complete genome structure and synthesis of infectious RNA from clones of tomato bushy stunt virus.
Hearne PQ, Knorr DA, Hillman BI, Morris TJ. Hearne PQ, et al. Among authors: knorr da. Virology. 1990 Jul;177(1):141-51. doi: 10.1016/0042-6822(90)90468-7. Virology. 1990. PMID: 2353450
Gene I, a potential cell-to-cell movement locus of cauliflower mosaic virus, encodes an RNA-binding protein.
Citovsky V, Knorr D, Zambryski P. Citovsky V, et al. Among authors: knorr d. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2476-80. doi: 10.1073/pnas.88.6.2476. Proc Natl Acad Sci U S A. 1991. PMID: 11607169 Free PMC article.
Identification of molecular defects causing congenital adrenal hyperplasia by cloning and differential hybridization of polymerase chain reaction-amplified 21-hydroxylase (CYP21) genes.
Helmberg A, Tabarelli M, Fuchs MA, Keller E, Dobler G, Schnegg I, Knorr D, Albert E, Kofler R. Helmberg A, et al. Among authors: knorr d. DNA Cell Biol. 1992 Jun;11(5):359-68. doi: 10.1089/dna.1992.11.359. DNA Cell Biol. 1992. PMID: 1605859
Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.
Krone N, Braun A, Roscher AA, Knorr D, Schwarz HP. Krone N, et al. Among authors: knorr d. J Clin Endocrinol Metab. 2000 Mar;85(3):1059-65. doi: 10.1210/jcem.85.3.6441. J Clin Endocrinol Metab. 2000. PMID: 10720040 Clinical Trial.
Prenatal diagnosis of 21-hydroxylase deficiency by RFLP analysis of the 21-hydroxylase, complement C4, and HLA class II genes.
Keller E, Andreas A, Scholz S, Dörr HC, Knorr D, Albert ED. Keller E, et al. Among authors: knorr d. Prenat Diagn. 1991 Nov;11(11):827-40. doi: 10.1002/pd.1970111104. Prenat Diagn. 1991. PMID: 1684434
Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal life.
Kuhnle U, Böhm N, Wolff G, Mayerová A, Dörr HG, Bidlingmaier F, Knorr D. Kuhnle U, et al. Among authors: knorr d. J Clin Endocrinol Metab. 1984 Mar;58(3):574-7. doi: 10.1210/jcem-58-3-574. J Clin Endocrinol Metab. 1984. PMID: 6607266
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