OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Advanced
Search
23
Results
Show all
Save search
Copy query
Show results for
Unknown
(17)
Proteomics
(6)
Organisms
Mus musculus
(5)
Homo sapiens
(2)
Repository
pride
(6)
Tissue
Testis
(3)
Cell culture
(2)
Fibroblast
(2)
Sperm
(2)
Embryo
(1)
Embryonic stem cell
(1)
Disease
Ciliopathy
(2)
Disease free
(2)
Technology Type
Affinity purification coupled with mass spectrometry proteomics
(6)
Mass Spectrometry
(6)
Shotgun proteomics
(4)
Publication Date
2021
(3)
2020
(2)
2018
(1)
Release Date
2007
(3)
2021
(2)
2018
(2)
2015
(2)
2014
(2)
2013
(2)
2019
(1)
2017
(1)
2012
(1)
2004
(1)
Lab affiliation
Medical Bioanalytics Institute for Ophthalmic Research Eberhard-Karls-University Tuebingen
(2)
Medical bioanalytics Institute for ophthalmic research Eberhard-Karls-University Tuebingen
(2)
Medical Bioanalytics Institute for Ophthalmic Research Eberhard-Karls University of Tuebingen Elfriede-Aulhorn-Str. 5-7 D-72076 Tübingen
(1)
Medical Bioanalytics, Eberhard-Karls University Tuebingen
(1)
Previous
page
1 / 3
You're on page
1
page
2
page
3
Next
page
Sort
by:
Relevance
Page size
10
Premature myogenic differentiation and depletion of progenitor cells cause severe muscle hypotrophy in Delta1 mutants.
Not available
S-EPMC1766420
|
biostudies-literature
Cite
Activity of the mouse Notch ligand DLL1 is sensitive to C-terminal tagging in vivo.
Not available
S-EPMC8477538
|
biostudies-literature
Cite
WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos.
Not available
S-EPMC528888
|
biostudies-literature
Cite
Notch2, but not Notch1, is required for proximal fate acquisition in the mammalian nephron.
Not available
S-EPMC2613851
|
biostudies-literature
Cite
Generation of an 870 kb deletion encompassing the Skt/Etl4 locus by combination of inter- and intra-chromosomal recombination.
Not available
S-EPMC4683868
|
biostudies-literature
Cite
Context-Dependent Functional Divergence of the Notch Ligands DLL1 and DLL4 In Vivo.
Not available
S-EPMC4482573
|
biostudies-literature
Cite
The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice.
Not available
S-EPMC6168554
|
biostudies-literature
Cite
The ectodomains determine ligand function in vivo and selectivity of DLL1 and DLL4 toward NOTCH1 and NOTCH2 in vitro.
Not available
S-EPMC6202052
|
biostudies-literature
Cite
S/T phosphorylation of DLL1 is required for full ligand activity in vitro but dispensable for DLL1 function in vivo during embryonic patterning and marginal zone B cell development.
Not available
S-EPMC3993573
|
biostudies-literature
Cite
Identification of the Cfap206 interactome from mouse testis to identify its role in cilia function
Cfap206 was immunoprecipitated from mouse testis to identify the interactome of this protein for further functional studies.
ORGANISM(S):
Mus musculus (Mouse)
2020-05-29
|
PXD018554
|
Pride
Mouse testis
Cfap206
Cite
Previous
page
1 / 3
You're on page
1
page
2
page
3
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets