210 related articles for article (PubMed ID: 37160609)
1. Knockout mouse models as a resource for the study of rare diseases.
da Silva-Buttkus P; Spielmann N; Klein-Rodewald T; Schütt C; Aguilar-Pimentel A; Amarie OV; Becker L; Calzada-Wack J; Garrett L; Gerlini R; Kraiger M; Leuchtenberger S; Östereicher MA; Rathkolb B; Sanz-Moreno A; Stöger C; Hölter SM; Seisenberger C; Marschall S; Fuchs H; Gailus-Durner V; Hrabě de Angelis M
Mamm Genome; 2023 Jun; 34(2):244-261. PubMed ID: 37160609
[TBL] [Abstract][Full Text] [Related]
2. Predicting human disease mutations and identifying drug targets from mouse gene knockout phenotyping campaigns.
Brommage R; Powell DR; Vogel P
Dis Model Mech; 2019 May; 12(5):. PubMed ID: 31064765
[TBL] [Abstract][Full Text] [Related]
3. Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes.
Higgins K; Moore BA; Berberovic Z; Adissu HA; Eskandarian M; Flenniken AM; Shao A; Imai DM; Clary D; Lanoue L; Newbigging S; Nutter LMJ; Adams DJ; Bosch F; Braun RE; Brown SDM; Dickinson ME; Dobbie M; Flicek P; Gao X; Galande S; Grobler A; Heaney JD; Herault Y; de Angelis MH; Chin HG; Mammano F; Qin C; Shiroishi T; Sedlacek R; Seong JK; Xu Y; ; Lloyd KCK; McKerlie C; Moshiri A
Sci Rep; 2022 Dec; 12(1):20791. PubMed ID: 36456625
[TBL] [Abstract][Full Text] [Related]
4. The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.
Groza T; Gomez FL; Mashhadi HH; Muñoz-Fuentes V; Gunes O; Wilson R; Cacheiro P; Frost A; Keskivali-Bond P; Vardal B; McCoy A; Cheng TK; Santos L; Wells S; Smedley D; Mallon AM; Parkinson H
Nucleic Acids Res; 2023 Jan; 51(D1):D1038-D1045. PubMed ID: 36305825
[TBL] [Abstract][Full Text] [Related]
5. Knockout mice are an important tool for human monogenic heart disease studies.
Cacheiro P; Spielmann N; Mashhadi HH; Fuchs H; Gailus-Durner V; Smedley D; de Angelis MH
Dis Model Mech; 2023 May; 16(5):. PubMed ID: 36825469
[TBL] [Abstract][Full Text] [Related]
6. New models for human disease from the International Mouse Phenotyping Consortium.
Cacheiro P; Haendel MA; Smedley D;
Mamm Genome; 2019 Jun; 30(5-6):143-150. PubMed ID: 31127358
[TBL] [Abstract][Full Text] [Related]
7. The mouse resource at National Resource Center for Mutant Mice.
Ju C; Liang J; Zhang M; Zhao J; Li L; Chen S; Zhao J; Gao X
Mamm Genome; 2022 Mar; 33(1):143-156. PubMed ID: 35138443
[TBL] [Abstract][Full Text] [Related]
8. The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data.
Koscielny G; Yaikhom G; Iyer V; Meehan TF; Morgan H; Atienza-Herrero J; Blake A; Chen CK; Easty R; Di Fenza A; Fiegel T; Grifiths M; Horne A; Karp NA; Kurbatova N; Mason JC; Matthews P; Oakley DJ; Qazi A; Regnart J; Retha A; Santos LA; Sneddon DJ; Warren J; Westerberg H; Wilson RJ; Melvin DG; Smedley D; Brown SD; Flicek P; Skarnes WC; Mallon AM; Parkinson H
Nucleic Acids Res; 2014 Jan; 42(Database issue):D802-9. PubMed ID: 24194600
[TBL] [Abstract][Full Text] [Related]
9. Multivariate phenotype analysis enables genome-wide inference of mammalian gene function.
Nicholson G; Morgan H; Ganjgahi H; Brown SDM; Mallon AM; Holmes C
PLoS Biol; 2022 Aug; 20(8):e3001723. PubMed ID: 35944064
[TBL] [Abstract][Full Text] [Related]
10. INFRAFRONTIER: a European resource for studying the functional basis of human disease.
Raess M; de Castro AA; Gailus-Durner V; Fessele S; Hrabě de Angelis M;
Mamm Genome; 2016 Aug; 27(7-8):445-50. PubMed ID: 27262858
[TBL] [Abstract][Full Text] [Related]
11. A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice.
Lindovsky J; Nichtova Z; Dragano NRV; Pajuelo Reguera D; Prochazka J; Fuchs H; Marschall S; Gailus-Durner V; Sedlacek R; Hrabě de Angelis M; Rozman J; Spielmann N
Mamm Genome; 2023 Jun; 34(2):107-122. PubMed ID: 37326672
[TBL] [Abstract][Full Text] [Related]
12. The pooling of manpower and resources through the establishment of European reference networks and rare disease patient registries is a necessary area of collaboration for rare renal disorders.
Parker S
Nephrol Dial Transplant; 2014 Sep; 29 Suppl 4():iv9-14. PubMed ID: 25165190
[TBL] [Abstract][Full Text] [Related]
13. Rapid phenotyping of knockout mice to identify genetic determinants of bone strength.
Freudenthal B; Logan J; ; Croucher PI; Williams GR; Bassett JH
J Endocrinol; 2016 Oct; 231(1):R31-46. PubMed ID: 27535945
[TBL] [Abstract][Full Text] [Related]
14. A mouse informatics platform for phenotypic and translational discovery.
Ring N; Meehan TF; Blake A; Brown J; Chen CK; Conte N; Di Fenza A; Fiegel T; Horner N; Jacobsen JO; Karp N; Lawson T; Mason JC; Matthews P; Morgan H; Relac M; Santos L; Smedley D; Sneddon D; Pengelly A; Tudose I; Warren JW; Westerberg H; Yaikhom G; Parkinson H; Mallon AM
Mamm Genome; 2015 Oct; 26(9-10):413-21. PubMed ID: 26314589
[TBL] [Abstract][Full Text] [Related]
15. Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Meehan TF; Conte N; West DB; Jacobsen JO; Mason J; Warren J; Chen CK; Tudose I; Relac M; Matthews P; Karp N; Santos L; Fiegel T; Ring N; Westerberg H; Greenaway S; Sneddon D; Morgan H; Codner GF; Stewart ME; Brown J; Horner N; ; Haendel M; Washington N; Mungall CJ; Reynolds CL; Gallegos J; Gailus-Durner V; Sorg T; Pavlovic G; Bower LR; Moore M; Morse I; Gao X; Tocchini-Valentini GP; Obata Y; Cho SY; Seong JK; Seavitt J; Beaudet AL; Dickinson ME; Herault Y; Wurst W; de Angelis MH; Lloyd KCK; Flenniken AM; Nutter LMJ; Newbigging S; McKerlie C; Justice MJ; Murray SA; Svenson KL; Braun RE; White JK; Bradley A; Flicek P; Wells S; Skarnes WC; Adams DJ; Parkinson H; Mallon AM; Brown SDM; Smedley D
Nat Genet; 2017 Aug; 49(8):1231-1238. PubMed ID: 28650483
[TBL] [Abstract][Full Text] [Related]
16. INFRAFRONTIER--providing mutant mouse resources as research tools for the international scientific community.
INFRAFRONTIER Consortium
Nucleic Acids Res; 2015 Jan; 43(Database issue):D1171-5. PubMed ID: 25414328
[TBL] [Abstract][Full Text] [Related]
17. Disrupting the male germ line to find infertility and contraception targets.
Archambeault DR; Matzuk MM
Ann Endocrinol (Paris); 2014 May; 75(2):101-8. PubMed ID: 24793995
[TBL] [Abstract][Full Text] [Related]
18. A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders.
Formosa MM; Bergen DJM; Gregson CL; Maurizi A; Kämpe A; Garcia-Giralt N; Zhou W; Grinberg D; Ovejero Crespo D; Zillikens MC; Williams GR; Bassett JHD; Brandi ML; Sangiorgi L; Balcells S; Högler W; Van Hul W; Mäkitie O
Front Endocrinol (Lausanne); 2021; 12():709711. PubMed ID: 34539568
[TBL] [Abstract][Full Text] [Related]
19. Uncovering Missing Heritability in Rare Diseases.
Maroilley T; Tarailo-Graovac M
Genes (Basel); 2019 Apr; 10(4):. PubMed ID: 30987386
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]