Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Anders Aamann Rasmussen"'
Autor:
Dorthe G. Crüger, Anders Jakobsen, Jan Lindebjerg, Kathleen D. Danenberg, Hidekazu Kuramochi, Lene Byriel, Lars Henrik Jensen, Peter V. Danenberg, Anders Aamann Rasmussen
Publikováno v:
Jensen, L H, Rasmussen, A A, Byriel, L, Kuramochi, H, Crüger, D G, Lindebjerg, J, Danenberg, P V, Jakobsen, A & Danenberg, K 2013, ' Regulation of MLH1 mRNA and protein expression by promoter methylation in primary colorectal cancer : a descriptive and prognostic cancer marker study ', Cellular Oncology, vol. 36, no. 5, pp. 411-419 . https://doi.org/10.1007/s13402-013-0148-2
Background In colorectal cancer MLH1 deficiency causes microsatellite instability, which is relevant for the patient's prognosis and treatment, and its putative heredity. Dysfunction of MLH1 is caused by sporadic gene promoter hypermethylation or by
Publikováno v:
University of Southern Denmark
Enteric bacteria respond to misfolded proteins by activating the transcription of "heat shock" genes. These genes are arranged in two major regulons controlled by the alternative sigma factors sigmaH and sigmaE. The two transcription factors coordina
Publikováno v:
Journal of Bacteriology. 185:5452-5464
In response to starvation,Myxococcus xanthusinitiates a developmental program that results in the formation of spore-filled multicellular fruiting bodies. Fruiting body formation depends on the temporal and spatial coordination of aggregation and spo
Autor:
Mette Warming Joergensen, Lone Sunde, Inge Agerholm, J. Hindkjær, Anders Aamann Rasmussen, Lars Bolund, Isa Niemann
Publikováno v:
Joergensen, M W, Niemann, I, Rasmussen, A A, Hindkjaer, J, Agerholm, I, Bolund, L & Sunde, L 2014, ' Triploid pregnancies, genetic and clinical features of 158 cases ', American Journal of Obstetrics and Gynecology . https://doi.org/10.1016/j.ajog.2014.03.039
Jørgensen, M W, Niemann, I, Rasmussen, AA, Hindkjaer, J, Agerholm, I, Bolund, L & Sunde, L 2014, ' Triploid pregnancies: genetic and clinical features of 158 cases ', American Journal of Obstetrics and Gynecology, vol. 211, no. 4, pp. 370.e1-370.e19 . https://doi.org/10.1016/j.ajog.2014.03.039
Jørgensen, M W, Niemann, I, Rasmussen, AA, Hindkjaer, J, Agerholm, I, Bolund, L & Sunde, L 2014, ' Triploid pregnancies: genetic and clinical features of 158 cases ', American Journal of Obstetrics and Gynecology, vol. 211, no. 4, pp. 370.e1-370.e19 . https://doi.org/10.1016/j.ajog.2014.03.039
OBJECTIVE: The purpose of this study was to analyze the correlation between the genetic constitution and the phenotype in triploid pregnancies. STUDY DESIGN: One hundred fifty-eight triploid pregnancies were identified in hospitals in Western Denmark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fa98f19644d07060eca4847395a3947
https://pure.au.dk/portal/da/publications/triploid-pregnancies-genetic-and-clinical-features-of-158-cases(f30949b4-e30c-428b-8857-30d0d2d7919c).html
https://pure.au.dk/portal/da/publications/triploid-pregnancies-genetic-and-clinical-features-of-158-cases(f30949b4-e30c-428b-8857-30d0d2d7919c).html
Autor:
Lilian Bomme Ousager, Christina Fagerberg, Charlotte K. Lautrup, Maria Kirchhoff, Anders Aamann Rasmussen, Niels H Birkebaek, Ulrike D. Heinl, Keld E. Sørensen, Inken Dreyer, Jesper Graakjaer
Publikováno v:
Fagerberg, C R, Graakjaer, J, Heinl, U D, Ousager, L B, Dreyer, I, Kirchhoff, E M, Rasmussen, A A, Lautrup, C K, Birkebæk, N & Sorensen, K 2013, ' Heart defects and other features of the 22q11 distal deletion syndrome ', European Journal of Medical Genetics, vol. 56, no. 2, pp. 98-107 . https://doi.org/10.1016/j.ejmg.2012.09.009
Fagerberg, C R, Graakjaer, J, Heinl, U D, Ousager, L B, Dreyer, I, Kirchhoff, E M, Rasmussen, A A, Lautrup, C K, Birkebaek, N & Sorensen, K 2013, ' Heart defects and other features of the 22q11 distal deletion syndrome ', European Journal of Medical Genetics, vol. 56, no. 2, pp. 98-107 . https://doi.org/10.1016/j.ejmg.2012.09.009
Fagerberg, C R, Graakjaer, J, Heinl, U D, Ousager, L B, Dreyer, I, Kirchhoff, E M, Rasmussen, A A, Lautrup, C K, Birkebaek, N & Sorensen, K 2013, ' Heart defects and other features of the 22q11 distal deletion syndrome ', European Journal of Medical Genetics, vol. 56, no. 2, pp. 98-107 . https://doi.org/10.1016/j.ejmg.2012.09.009
22q11.2 distal deletion syndrome is distinct from the common 22q11.2 deletion syndrome and caused by microdeletions localized adjacent to the common 22q11 deletion at its telomeric end. Most distal deletions of 22q11 extend from LCR22-4 to an LCR in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64b9e2ba48cb27c3258be4458db2e770
https://pure.au.dk/portal/da/publications/heart-defects-and-other-features-of-the-22q11-distal-deletion-syndrome(543e15f8-3560-49b2-b41a-34dcbadd08ba).html
https://pure.au.dk/portal/da/publications/heart-defects-and-other-features-of-the-22q11-distal-deletion-syndrome(543e15f8-3560-49b2-b41a-34dcbadd08ba).html
Autor:
Anne-Bine, Skytte, Marianne, Waldstrøm, Anders Aamann, Rasmussen, Dorthe, Crüger, Emma R, Woodward, Steen, Kølvraa
Publikováno v:
Acta obstetricia et gynecologica Scandinavica. 90(6)
It is believed that 24-40% of ovarian cancers have dysfunction in the BRCA1 or BRCA2 (BRCAness) genes, due to either inherited or somatic mutations or due to epigenetic inactivation. Demonstration of ovarian cancers with BRCAness is becoming importan
Autor:
Evan T. Powers, Ulrik H Eriksen, Anders Aamann Rasmussen, Christina Fagerberg, Minna Groenning, Raul I Campos, Per Hammarström
Publikováno v:
Groenning, M, Campos, R I, Fagerberg, C, Rasmussen, A A, Eriksen, U H, Powers, E T & Hammarström, P 2011, ' Thermodynamic stability and denaturation kinetics of a benign natural transthyretin mutant identified in a Danish kindred ', Amyloid: the Journal of Protein Folding Disorders, vol. 18, no. 2, pp. 35-46 . https://doi.org/10.3109/13506129.2011.560215
The disease phenotype of transthyretin (TTR) is dramatically influenced by single point mutations in the TTR gene. Herein, we report on a novel mutation D99N (Asp99Asn) in TTR found in a Danish kindred. None of the family members carrying this mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da37b91a72a46310db25de50a6726c46
https://portal.findresearcher.sdu.dk/da/publications/8cdae294-ee79-43e1-851b-faf0ad91c5a3
https://portal.findresearcher.sdu.dk/da/publications/8cdae294-ee79-43e1-851b-faf0ad91c5a3
Publikováno v:
Valentin-Hansen, P, Johansen, J & Rasmussen, A A 2007, ' Small RNAs controlling outer membrane porins ', Current Opinion in Microbiology, vol. 10, no. 2, pp. 152-155 . https://doi.org/10.1016/j.mib.2007.03.001
Udgivelsesdato: 2007-Apr Gene regulation by small non-coding RNAs has been recognized as an important post-transcriptional regulatory mechanism for several years. In Gram-negative bacteria such as Escherichia coli and Salmonella, these RNAs control s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d861de90bd2f6fe1e53ff46d6592c2b
https://portal.findresearcher.sdu.dk/da/publications/0b1397c0-de22-11dc-860c-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/0b1397c0-de22-11dc-860c-000ea68e967b
Autor:
Anders Aamann, Rasmussen, Maiken, Eriksen, Kambiz, Gilany, Christina, Udesen, Thomas, Franch, Carsten, Petersen, Poul, Valentin-Hansen
Publikováno v:
Molecular microbiology. 58(5)
The Escherichia coli ompA mRNA, encoding a highly abundant outer membrane protein, has served as a model for regulated mRNA decay in bacteria. The half-life of this transcript correlates inversely with the bacterial growth rate and is growth stage-de
Autor:
Flemming Brandt Sørensen, René dePont Christensen, Anne Marie Bak Jylling, Erik Jakobsen, Anders Aamann Rasmussen
Publikováno v:
Aarhus University
Bak Jylling, A M, Rasmussen, A A, Jakobsen, E H, Christensen, R D & Sørensen, F B 2014, ' Are mutations in K-RAS, BRAF and PIK3CA genes critical for response to adjuvant trastuzumab treatment in patients with HER-2 positive breast cancer? ', Journal of Cancer Therapeutics & Research, bind 3, nr. 3 .
Bak Jylling, A M, Rasmussen, A A, Jakobsen, E H, Christensen, R D & Sørensen, F B 2014, ' Are mutations in K-RAS, BRAF and PIK3CA genes critical for response to adjuvant trastuzumab treatment in patients with HER-2 positive breast cancer? ', Journal of Cancer Therapeutics & Research, bind 3, nr. 3, 3 .
Bak Jylling, A M, Rasmussen, A A, Jakobsen, E H, Christensen, R D & Sørensen, F B 2014, ' Are mutations in K-RAS, BRAF and PIK3CA genes critical for response to adjuvant trastuzumab treatment in patients with HER-2 positive breast cancer? ', Journal of Cancer Therapeutics & Research, bind 3, nr. 3 .
Bak Jylling, A M, Rasmussen, A A, Jakobsen, E H, Christensen, R D & Sørensen, F B 2014, ' Are mutations in K-RAS, BRAF and PIK3CA genes critical for response to adjuvant trastuzumab treatment in patients with HER-2 positive breast cancer? ', Journal of Cancer Therapeutics & Research, bind 3, nr. 3, 3 .
Background: HER-2 is a prognostic and predictive factor in patients suffering from breast cancer. Since 2006 we have tested routinely the HER-2 status in patients with primary breast cancer at Vejle Hospital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15a52a72e4e4dd0ea122a6164702ecf
https://pure.au.dk/portal/en/publications/are-mutations-in-kras-braf-and-pik3ca-genes-critical-for-response-to-adjuvant-trastuzumab-treatment-in-patients-with-her2-positive-breast-cancer(c0666998-888a-4f0a-8cdf-eca765eb28c1).html
https://pure.au.dk/portal/en/publications/are-mutations-in-kras-braf-and-pik3ca-genes-critical-for-response-to-adjuvant-trastuzumab-treatment-in-patients-with-her2-positive-breast-cancer(c0666998-888a-4f0a-8cdf-eca765eb28c1).html