E-LIB Suche - Ergebnisse für: Amarie, O.V

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/..

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..

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..

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..