Zobrazeno 1 - 10
of 64
pro vyhledávání: '"T A, Kruse"'
Autor:
K Koutromanou, A Horn, Montserrat Fernandez-Rivas, N Ghaussy, T Møller Kruse, Hendrik Wolf, Eike Wüstenberg
Publikováno v:
Journal of investigational allergologyclinical immunology. 31(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d6fd3ef79c8e85e226e179dfb3b2f92
https://pubmed.ncbi.nlm.nih.gov/32573456
https://pubmed.ncbi.nlm.nih.gov/32573456
Autor:
I. M. H. Sønderstrup, M. B. Jensen, B. Ejlertsen, J. O. Eriksen, A. M. Gerdes, T. A. Kruse, M. J. Larsen, M. Thomassen, A. V. Laenkholm
Background: Patients with a BRCA1 or BRCA2 mutation (BRCA-mutated breast cancer) are frequently diagnosed with low differentiated and highly proliferating breast cancer characterized by high amounts of tumor-infiltrating lymphocytes (Tils). Stromal T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13dda912ac0157e45a9b1a09a71cfcd4
Autor:
Ole Faergeman, Steen Kølvraa, J.U. Brorholt-Petersen, Henrik Jensen, T. M. Christiansen, Jesper Møller Jensen, T. A. Kruse
Publikováno v:
Annals of Human Genetics. 63:511-520
Most studies of the pathogenesis of coronary heart disease occur between gene variants and biochemical or physiological variables known to be atherogenic. In many situations, however, the gene products are not necessarily known. We studied 17 familie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de48eb336e3646615d5672569b82d907
https://doi.org/10.1046/j.1469-1809.1999.6360511.x
https://doi.org/10.1046/j.1469-1809.1999.6360511.x
Autor:
T J Kruse, Sheng-Chin Kung, John C. Hemminger, Matthew A. Brown, Yongan Yang, David K. Taggart, Aleix G. Güell, Reginald M. Penner, Chengxiang Xiang, Fan Yang
Publikováno v:
Nano letters. 8(8)
We describe the preparation by electrodeposition of arrays of lead telluride (PbTe) nanowires using the lithographically patterned nanowire electrodeposition (LPNE) method. PbTe nanowires had a rectangular cross-section with adjustable width and heig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6209e0c62664aec3e587d8d4abb4872c
https://pubmed.ncbi.nlm.nih.gov/18624390
https://pubmed.ncbi.nlm.nih.gov/18624390
Publikováno v:
Clinical genetics. 69(2)
To meet the increasing demand for BRCA1 and BRCA2 mutation analysis, a robust system for selecting families who have a higher chance of a mutation has become important. Several models have been developed to help predict which samples are more likely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b423ad6e926c88024aa43287367ea001
https://pubmed.ncbi.nlm.nih.gov/16433698
https://pubmed.ncbi.nlm.nih.gov/16433698
Publikováno v:
Clinical genetics. 68(3)
We report an approach for BRCA1/2 testing whereby genetic testing can be offered to families at high risk of hereditary breast and ovarian cancer but where no DNA from affected relatives is available. By testing two or more unaffected relatives at 50
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::505f795774089b7c81265c4f6e5405e1
https://pubmed.ncbi.nlm.nih.gov/16098011
https://pubmed.ncbi.nlm.nih.gov/16098011
Autor:
M D, Lundorf, H N, Buttenschøn, L, Foldager, D H R, Blackwood, W J, Muir, V, Murray, A J, Pelosi, T A, Kruse, H, Ewald, O, Mors
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)
Recent evidence from postmortem studies suggests that GAD1 encoding the gamma-aminobutyric acid (GABA) synthetic enzyme GAD67 is a functional candidate susceptibility gene for both bipolar affective disorder (BPAD) and schizophrenia. Previous studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9887b7884c0d0cbd86a2ad5629a507e3
https://pubmed.ncbi.nlm.nih.gov/15806582
https://pubmed.ncbi.nlm.nih.gov/15806582
Autor:
Q, Tan, L, Christiansen, L, Bathum, J H, Zhao, W, Vach, J W, Vaupel, K, Christensen, T A, Kruse
Publikováno v:
Annals of human genetics. 69(Pt 2)
Haplotype based linkage disequilibrium (LD) mapping exhibits higher power than the single locus approach because it makes use of the LD information contained in the flanking markers. New statistical methods have been proposed to help to infer haploty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::572a970264d05db2d70eb11d6f911f26
https://pubmed.ncbi.nlm.nih.gov/15720298
https://pubmed.ncbi.nlm.nih.gov/15720298
Autor:
H, Ewald, F P, Wikman, B M, Teruel, H N, Buttenschön, M, Torralba, T D, Als, A, El Daoud, T J, Flint, T H, Jorgensen, L, Blanco, T A, Kruse, T F, Orntoft, O, Mors
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (1)
Homozygosity mapping is a very powerful method for finding rare recessive disease genes in monogenic disorders and may also be useful for locating risk genes in complex disorders, late onset disorders where parents often are not available, and for ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81427281b3784f7d2dbc553d9cb24aa3
https://pubmed.ncbi.nlm.nih.gov/15558715
https://pubmed.ncbi.nlm.nih.gov/15558715
Autor:
K, Brusgaard, A D, Kjeldsen, L, Poulsen, H, Moss, P, Vase, K, Rasmussen, T A, Kruse, M, Hørder
Publikováno v:
Clinical genetics. 66(6)
Hereditary haemorrhagic telangiectasia (HHT) is a rare disorder with one per 6000-10,000 affected individuals in the general Caucasian population. HHT is genetically heterogeneous, involving at least two loci HHT1 mapping to chromosome 9q34.1 and HHT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::43dbcc693406668e53f58d61aec5ac7f
https://pubmed.ncbi.nlm.nih.gov/15521985
https://pubmed.ncbi.nlm.nih.gov/15521985