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Results: 1-25/49
Authors:
Krohn, K
Paschke, R
Citation: K. Krohn et R. Paschke, Loss of heterozygocity at the thyroid peroxidase gene locus in solitary cold thyroid nodules, THYROID, 11(8), 2001, pp. 741-747
Authors:
Wallaschofski, H
Orda, C
Fuhrer, D
Holzapfel, HP
Krohn, K
Miehle, K
Neumann, S
Georgi, P
Paschke, R
Citation: H. Wallaschofski et al., Distinction between autoimmune and nonautoimmune hyperthyroidism by determination of thyrotropin-receptor antibodies in patients with the scintigraphic diagnosis of disseminated autonomy, THYROID, 11(7), 2001, pp. 710-711
Authors:
Eszlinger, M
Krohn, K
Kratzsch, J
Voigt, C
Paschke, R
Citation: M. Eszlinger et al., Growth factor expression in cold and hot thyroid nodules, THYROID, 11(2), 2001, pp. 125-135
Authors:
Klemm, T
Neumann, S
Trulzsch, B
Pistrosch, F
Hanefeld, M
Paschke, R
Citation: T. Klemm et al., Search for mitochondrial DNA, mutation ate position 3243 in German patients with a positive family history of maternal diabetes mellitus, EXP CL E D, 109(5), 2001, pp. 283-287
Authors:
Lohmann, T
Kratzsch, J
Kellner, K
Witzigmann, H
Hauss, J
Paschke, R
Citation: T. Lohmann et al., Severe hypoglycemia due to insulin autoimmune syndrome with autoantibodiescrossreactive to proinsulin, EXP CL E D, 109(4), 2001, pp. 245-248
Authors:
Paschke, R
Neumann, S
Citation: R. Paschke et S. Neumann, Sodium/iodide symporter mRNA expression in cold thyroid nodules, EXP CL E D, 109(1), 2001, pp. 45-46
Authors:
Trulzsch, B
Krohn, K
Wonerow, P
Chey, S
Holzapfel, HP
Ackermann, F
Fuhrer, D
Paschke, R
Citation: B. Trulzsch et al., Detection of thyroid-stimulating hormone receptor and G(s)alpha mutations:in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis, J MOL MED-J, 78(12), 2001, pp. 684-691
Authors:
Neumann, S
Krause, G
Chey, S
Paschke, R
Citation: S. Neumann et al., A free carboxylate oxygen in the side chain of position 674 in transmembrane domain 7 is necessary for TSH receptor activation, MOL ENDOCR, 15(8), 2001, pp. 1294-1305
Frequency of the calcium-sensing receptor variant A986S in patients with primary hyperparathyroidism
Authors:
Miedlich, S
Lamesch, P
Mueller, A
Paschke, R
Citation: S. Miedlich et al., Frequency of the calcium-sensing receptor variant A986S in patients with primary hyperparathyroidism, EUR J ENDOC, 145(4), 2001, pp. 421-427
Authors:
Krohn, K
Reske, A
Ackermann, F
Muller, A
Paschke, R
Citation: K. Krohn et al., Ras mutations are rare in solitary cold and toxic thyroid nodules, CLIN ENDOCR, 55(2), 2001, pp. 241-248
Authors:
Bluher, M
Kratzsch, J
Paschke, R
Citation: M. Bluher et al., Plasma levels of tumor necrosis factor-alpha, angiotensin II, growth hormone, and IGF-1 are not elevated in insulin-resistant obese individuals with impaired glucose tolerance, DIABET CARE, 24(2), 2001, pp. 328-334
Authors:
Krohn, K
Paschke, R
Citation: K. Krohn et R. Paschke, Progress in understanding the etiology of thyroid autonomy, J CLIN END, 86(7), 2001, pp. 3336-3345
Authors:
Eszlinger, M
Krohn, K
Paschke, R
Citation: M. Eszlinger et al., Complementary DNA expression array analysis suggests a lower expression ofsignal transduction proteins and receptors in cold and hot thyroid nodules, J CLIN END, 86(10), 2001, pp. 4834-4842
Authors:
Zhang, J
Martasek, P
Paschke, R
Shea, T
Masters, BSS
Kim, JJP
Citation: J. Zhang et al., Crystal structure of the FAD/NADPH-binding domain of rat neuronal nitric-oxide synthase - Comparisons with NADPH-cytochrome P450 oxidoreductase, J BIOL CHEM, 276(40), 2001, pp. 37506-37513
Authors:
Hubbard, PA
Shen, AL
Paschke, R
Kasper, CB
Kim, JJP
Citation: Pa. Hubbard et al., NADPH-cytochrome P450 oxidoreductase - Structural basis for hydride and electron transfer, J BIOL CHEM, 276(31), 2001, pp. 29163-29170
Authors:
Wallaschofski, H
Orda, C
Georgi, P
Miehle, K
Paschke, R
Citation: H. Wallaschofski et al., Distinction between autoimmune and non-autoimmune hyperthyroidism by determination of TSH-receptor antibodies in patients with the initial diagnosis of toxic multinodular goiter, HORMONE MET, 33(8), 2001, pp. 504-507
Authors:
Neumann, S
Krohn, K
Chey, S
Paschke, R
Citation: S. Neumann et al., Mutations in the mouse TSH receptor equivalent to human constitutively activating TSH receptor mutations also cause constitutive activity, HORMONE MET, 33(5), 2001, pp. 263-269
Authors:
Fasshauer, M
Klein, J
Neumann, S
Eszlinger, M
Paschke, R
Citation: M. Fasshauer et al., Adiponectin gene expression is inhibited by beta-adrenergic stimulation via protein kinase A in 3T3-L1 adipocytes, FEBS LETTER, 507(2), 2001, pp. 142-146
Authors:
Fasshauer, M
Kein, J
Neumann, S
Eszlinger, M
Paschke, R
Citation: M. Fasshauer et al., Isoproterenol inhibits resistin gene expression through a G(S)-protein-coupled pathway in 3T3-L1 adipocytes, FEBS LETTER, 500(1-2), 2001, pp. 60-63
Authors:
Reichenberger, F
Wirtz, H
Paschke, R
Citation: F. Reichenberger et al., Clopidogrel and side effects, CARDIOLOGY, 96(1), 2001, pp. 51-52
Authors:
Fasshauer, M
Klein, J
Neumann, S
Eszlinger, M
Paschke, R
Citation: M. Fasshauer et al., Tumor necrosis factor alpha is a negative regulator of resistin gene expression and secretion in 3T3-L1 adipocytes, BIOC BIOP R, 288(4), 2001, pp. 1027-1031
Authors:
Dunger, S
Neumann, S
Zell, R
Birch-Hirschfeld, E
Stelzner, A
Paschke, R
Kinne, RW
Sickinger, S
Citation: S. Dunger et al., Mutation detection in mosaic situations: RNA mismatch assay and denaturinggradient gel electrophoresis are more sensitive than conventional cycle sequencing, ANALYT BIOC, 294(1), 2001, pp. 89-93
Authors:
Fuhrer, D
Warner, J
Sequeira, M
Paschke, R
Gregory, J
Ludgate, M
Citation: D. Fuhrer et al., Novel TSHR germline mutation (Met463Val) masquerading as Graves' disease in a large Welsh kindred with hyperthyroidism, THYROID, 10(12), 2000, pp. 1035-1041
Authors:
Wallaschofski, H
Kaczmarek, M
Miehle, K
Hentschel, B
Paschke, R
Citation: H. Wallaschofski et al., Differences between thyrotropin receptor antibody bioactivity and inhibition of I-125-bovine thyrotropin binding, THYROID, 10(10), 2000, pp. 897-907
Authors:
Miedlich, S
Krohn, K
Lamesch, P
Muller, A
Paschke, R
Citation: S. Miedlich et al., Frequency of somatic MEN1 gene mutations in monoclonal parathyroid tumoursof patients with primary hyperparathyroidism, EUR J ENDOC, 143(1), 2000, pp. 47-54