Zobrazeno 1 - 10
of 756
pro vyhledávání: '"B. H. Weber"'
Autor:
Chien Y; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Wu YR; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Chen CY; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Yang YP; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Food Safety and Health Risk Assessment, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Ching LJ; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Clinical Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Wang BX; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Chang WC; Center for Molecular Medicine, China Medical University Hospital, Taichung, 40447, Taiwan., Chiang IH; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan., Su P; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan., Chen SY; Institute of Biomedical Sciences, Academia Sinica, Taipei, 11529, Taiwan.; Genome and Systems Biology Degree Program, Academia Sinica and National Taiwan University, Taipei, 10617, Taiwan., Lin WC; Institute of Biomedical Sciences, Academia Sinica, Taipei, 11529, Taiwan.; Institute of Biomedical Informatics, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Wang IC; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan., Lin TC; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan.; Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, 112201, Taiwan., Chen SJ; School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan.; Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, 112201, Taiwan., Chiou SH; Department of Medical Research, Taipei Veterans General Hospital, Taipei, 11217, Taiwan.; Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan.; Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, 112201, Taiwan.; Genomics Research Center, Academia Sinica, Taipei, 11529, Taiwan.
Publikováno v:
Advanced science (Weinheim, Baden-Wurttemberg, Germany) [Adv Sci (Weinh)] 2024 Nov 06, pp. e2405818. Date of Electronic Publication: 2024 Nov 06.
Autor:
Shirodkar, Kapil K.1 (AUTHOR), Jenko, Nathan1 (AUTHOR), Azzopardi, Christine1 (AUTHOR), Murphy, Jennifer1 (AUTHOR), Patel, Anish1 (AUTHOR), James, Steven L.1 (AUTHOR), Davies, Arthur Mark1 (AUTHOR), Botchu, Rajesh1 (AUTHOR) drbrajesh@yahoo.com
Publikováno v:
Indian Journal of Radiology & Imaging. Jan2025, Vol. 35 Issue 1, p59-66. 8p.
Autor:
Tian, Xiang1 (AUTHOR) emy_xiang@sjtu.edu.cn
Publikováno v:
SAGE Open. Jul-Sep2024, Vol. 14 Issue 3, p1-17. 17p.
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 226(12)
Hereditary retinal dystrophies comprise a heterogeneous group of inherited retinal disorders with variable clinical presentation and multiple associated genes. Clinical diagnosis and differential diagnosis are difficult. The purpose of the current pa
Autor:
J, Chang-Claude, H, Becher, M, Caligo, D, Eccles, G, Evans, N, Haites, S, Hodgson, P, Møller, B H, Weber, D, Stoppa-Lyonnet
Publikováno v:
Disease Markers
For genetic counselling of a woman on familial breast cancer, an accurate evaluation of the probability that she carries a germ-line mutation is needed to assist in making decisions about genetic-testing. We used data from eight collaborating centres
Autor:
U, Felbor, B H, Weber
Publikováno v:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 95(5)
The recent identification of the tissue inhibitor of metalloproteinases-3 (TIMP3) as the gene underlying SFD pathology has made it possible to address the question of genetic heterogeneity in this disorder. In addition, it now has become feasible to
Publikováno v:
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 6(3)
We have localized a second gene for membrane-type matrix metalloproteinases, MT2-MMP, to chromosome 16q12 by in situ hybridization. FISH experiments using a genomic PAC clone containing the MT2-MMP gene resulted in an unusual hybridization pattern de
Publikováno v:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 95(1)
North Carolina macular dystrophy (NCMD) is a rare autosomal dominant maculopathy with highly variable expressivity. Genetic analysis of an American family consisting of 247 members out of which 96 were affected with NCMD allowed chromosomal assignmen
Publikováno v:
Cancer genetics and cytogenetics. 102(1)
Autor:
B H, Weber
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 210(1)
Hereditary macular degeneration comprise a large group of disorders characterized by a preferential loss of central vision due to degenerative changes in the macular area of the retina. The primary causes underlying these degenerative processes are u