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Amarie, O.V
64
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Online (64)
Mediatypes
Articles (Online) (24)
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english (59)
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1
Splice‐site mutation in the Bmpr1b gene of the mouse causes..:
Graw, J.
;
Yan, X.
;
Amarie, O.V.
...
Acta Ophthalmologica. 94 (2016) S256 - p. , 2016
Link:
https://doi.org/10.1111/..
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2
Novel mouse phenotypes identified in the eye screen of the ..:
Amarie, O.V.
;
Fuchs, H.
;
Gailus‐Durner, V.
..
Acta Ophthalmologica. 93 (2015) S255 - p. , 2015
Link:
https://doi.org/10.1111/..
?
3
Deficiency in the expression of Vps13C is associated with a..:
Amarie, O.
;
Rathkolb, B.
;
Fuchs, H.
...
Acta Ophthalmologica. 95 (2017) S259 - p. , 2017
Link:
https://doi.org/10.1111/..
?
4
Single-cell, whole-embryo phenotyping of mammalian developm..:
Huang, X
;
Henck, J
;
Qiu, C
...
http://edoc.mdc-berlin.de/23876/1/23876oa.pdf. , 2023
Link:
http://edoc.mdc-berlin.d..
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5
Genome-wide screening reveals the genetic basis of mammalia..:
Chee J. M
;
Lanoue L
;
Clary D
...
info:eu-repo/semantics/altIdentifier/pmid/36737727. , 2023
Link:
https://hdl.handle.net/1..
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6
Post-synaptic scaffold protein TANC2 in psychiatric and som..:
Garrett, L
;
da Silva Buttkus, P
;
Rathkolb, B
...
info:eu-repo/semantics/altIdentifier/doi/10.1242/dmm.049205. , 2022
Link:
https://push-zb.helmholt..
?
7
N471D WASH complex subunit strumpellin knock-in mice displa..:
Clemen, C.S
;
Schmidt, A
;
Winter, L
...
info:eu-repo/semantics/altIdentifier/doi/10.1111/nan.12750. , 2022
Link:
https://push-zb.helmholt..
?
8
Validation of Mct8/Oatp1c1 dKO mice as a model organism for..:
Maity-Kumar, G
;
Ständer, L
;
de Angelis, M
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.molmet.2022.101616. , 2022
Link:
https://push-zb.helmholt..
?
9
Mice lacking the mitochondrial exonuclease MGME1 develop in..:
Milenkovic, D
;
Sanz-Moreno, A
;
Calzada-Wack, J
...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1010190. , 2022
Link:
https://push-zb.helmholt..
?
10
Mutations within the cGMP-binding domain of CNGA1 causing a..:
Kandaswamy, S
;
Zobel, L
;
John, B
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41420-022-01185-0. , 2022
Link:
https://push-zb.helmholt..
?
11
Extensive identification of genes involved in congenital an..:
Spielmann, N
;
Miller, G
;
Oprea, T.I
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s44161-022-00018-8. , 2022
Link:
https://push-zb.helmholt..
?
12
Deep phenotyping and lifetime trajectories reveal limited e..:
Xie, K
;
Fuchs, H
;
Scifo, E
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-022-34515-y. , 2022
Link:
https://push-zb.helmholt..
?
13
Mouse mutant phenotyping at scale reveals novel genes contr..:
Swan, A.L
;
Schütt, C
;
Rozman, J
...
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1009190. , 2021
Link:
https://push-zb.helmholt..
?
14
A comprehensive phenotypic characterization of a whole-body..:
Biagosch, C
;
Vidali, S
;
Faerberboeck, M
...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00335-021-09875-3. , 2021
Link:
https://push-zb.helmholt..
?
15
Characterising a homozygous two-exon deletion in UQCRH : Co..:
Vidali, S
;
Gerlini, R
;
Thompson, K
...
info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.202114397. , 2021
Link:
https://push-zb.helmholt..
1-15