Volltext-Artikel, E-Books und Literaturhinweise aus dem EBSCO Discovery Service
"Artikel & mehr" berücksichtigt nur einen Teil der für die Bibliothek der Frankfurt UAS verfügbaren Datenbanken. Zur Übersicht in DBIS
Ergebnis verändern
- Publikationstyp
Publikationstyp- erschienen in
- Verlag
- Geographic terms
-
1
von Bravo, Laura ; Simões, Joana FF ; Cardoso, Victor R ; et al.
In The Lancet Digital Health July 2024 6(7):e507-e519
-
2
von Weerts, MJA ; Lanko, K ; Guzman-Vega, FJ ; et al.
Genetics in Medicine (2021)
-
3
von Aldinger, KA ; Thomson, Z ; Phelps, IG ; et al.
Nature Neuroscience , 24 pp. 1163-1175. (2021)
Schlagworte: Development of the nervous system; Developmental biology; Molecular biology; Neuroscience; Transcriptomics
-
4
von Haldipur, P ; Aldinger, KA ; Bernardo, S ; et al.
Science , 366 (6464) pp. 454-460. (2019)
- 5
-
6
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
von Shah, S ; Schrader, KA ; Vijai, J ; et al.
urn:ISSN:1061-4036 ; urn:ISSN:1546-1718 ; Nature Genetics, 45, 10, 1226-1231
Schlagworte: 31 Biological Sciences; 3102 Bioinformatics and Computational Biology; 3105 Genetics; Rare Diseases; Hematology; Childhood Leukemia; Pediatric Cancer; Orphan Drug; Pediatric Research Initiative; Cancer; 2.1 Biological and endogenous factors; Genetic Predisposition to Disease; Germ-Line Mutation; Humans; PAX5 Transcription Factor; Polymorphism; Single Nucleotide; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma; anzsrc-for: 31 Biological Sciences; anzsrc-for: 3102 Bioinformatics and Computational Biology; anzsrc-for: 3105 Genetics; anzsrc-for: 06 Biological Sciences; anzsrc-for: 11 Medical and Health Sciences; anzsrc-for: 3001 Agricultural biotechnology
-
7
von Aldinger KA ; Thomson Z ; Phelps IG ; et al.
Nature Neuroscience, 2021
-
8
von Aldinger KA ; Timms AE ; Thomson Z ; et al.
American Journal of Human Genetics, 5 September 2019
-
9
von Aldinger, KA ; Timms, AE ; Thomson, Z ; et al.
Schlagworte: autism; cerebellar hypoplasia; cerebellum; Dandy-Walker malformation; epilepsy
-
10
von Dobyns, WB ; Aldinger, KA ; Ishak, G E ; et al.
Dobyns, WB, Aldinger, KA, Ishak, G E, Mirzaa, GM, Timms, AE, Grout, ME, Dremmen, M, Schot, R, Vandervore, L, van Slegtenhorst, M, Wilke, M, Kasteleijn, E, Lee, AS, Barry, BJ, Chao, KR, Szczaluba, K, Kobori, J, Hanson-Kahn, A, Bernstein, JA, Carr, L, D'Arco, F, Miyana, K, Okazaki, T, Saito, Y, Sasaki, M, Das, S, Wheeler, MM, Bamshad, MJ, Nickerson, DA, Engle, EC, Verheijen, F, Doherty, D & Verheijen - Mancini, G 2018, 'MACF1 Mutations Encoding Highly Conserved Zinc-Binding Residues of the GAR Domain Cause Defects in Neuronal Migration and Axon Guidance', American Journal of Human Genetics, vol. 103, no. ....
Schlagworte: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCNIHES033002; name=EMC NIHES-03-30-02
-
11
von Clarke, CM ; Fok, VT ; Gustafson, JA ; et al.
American Journal of Medical Genetics Part A ; volume 176, issue 11, page 2522-2522 ; ISSN 1552-4825 1552-4833
- 12
- 13
-
14
von SIMS AM ; TIMMS AE ; ARMAS BRUGES J ; et al.
Schlagworte: HLA-B27; Interleukin-1; Ankylosing Spondylitis
- 15
- 16
- 17
-
18
von Pointon, JJ ; Timms, AE ; Bradbury, L ; et al.
Schlagworte: Rheumatology
-
19
von Carter, KW ; Pluznhnikov, A ; Timms, AE ; et al.
Schlagworte: Rheumatology
-
20
von Sims, AM ; Timms, AE ; Bradbury, LA ; et al.
Schlagworte: Rheumatology
-
21
von Newton, JL ; Harney, SMJ ; Timms, AE ; et al.
Schlagworte: Rheumatology; Susceptibility; Nationwide; Genetics; Locus; Ra
-
22
Schlagworte: Genetics & Heredity; Polymorphisms; Spondylarthropathies; Population; Genotype; Cyp2d6; Family; Risk; Hla
-
23
von Timms, AE ; Zhang, Y ; Bradbury, L ; et al.
Schlagworte: Rheumatology; Posterior Longitudinal Ligament; Progressive Ankylosis; Craniometaphyseal Dysplasia; Animal-model; Spine Opll; Gene; Disease; Mouse; Susceptibility; Mutations
-
24
von Timms, AE ; Sathananthan, R ; Bradbury, L ; et al.
Schlagworte: Rheumatology; Hereditary Hemochromatosis; Hla-h; Hfe; Mutation; Prevalence; Expression; Population; Disease
-
25
von Timms, AE ; Zhang, Y ; Russell, RGG ; et al.
Schlagworte: Rheumatology; Posterior Longitudinal Ligament; Hereditary Articular Chondrocalcinosis; Nucleoside-triphosphate Pyrophosphatase; Inorganic Pyrophosphate; Craniometaphyseal Dysplasia; Familial Chondrocalcinosis; Ankylosing-spondylitis; Chromosome 5p; Mouse Model; Spine Opll
Hilfe & Kontakt ǀ Fernleihe | Hilfe zur Fernleihe ǀ Literaturvorschlag| Literaturvorschlag