OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Help
Advanced
Search
43
Results
Show all
Save search
Copy query
Show results for
Unknown
(37)
Genomics
(4)
Other
(1)
Proteomics
(1)
Organisms
Saccharomyces cerevisiae
(2)
Homo sapiens
(1)
Alphavirus
(1)
Betaherpesvirinae
(1)
Brassica oleracea var. oleracea
(1)
Cowpox virus
(1)
Coxsackievirus
(1)
Cytomegalovirus
(1)
Dengue virus
(1)
EFO:0001352
(1)
Filoviridae
(1)
Hepatitis B virus
(1)
Human alphaherpesvirus 1
(1)
Human betaherpesvirus 5
(1)
Human immunodeficiency virus
(1)
Human immunodeficiency virus 1
(1)
Human immunodeficiency virus 2
(1)
Influenza A virus
(1)
Influenza C virus
(1)
Japanese encephalitis virus
(1)
Japanese encephalitis virus group
(1)
Lyssavirus rabies
(1)
Monkeypox virus
(1)
Nostoc sp. PCC 7120 = FACHB-418
(1)
Oropouche virus
(1)
Orthopoxvirus
(1)
Orthopoxvirus vaccinia
(1)
Rattus
(1)
Ruditapes decussatus
(1)
Tick-borne encephalitis virus
(1)
Organisms
Saccharomyces cerevisiae
(2)
Repository
geo
(2)
ENA
(2)
EGA
(1)
pride
(1)
Tissue
Cell culture
(1)
Technology Type
Gel-based experiment
(1)
Mass Spectrometry
(1)
Shotgun proteomics
(1)
Release Date
2023
(6)
2024
(5)
2022
(5)
2017
(4)
2015
(4)
2019
(3)
2021
(2)
2020
(2)
2025
(1)
2018
(1)
2014
(1)
2013
(1)
2012
(1)
2011
(1)
Lab affiliation
MRC Protein Phosphorylation & Ubiquitylation Unit, University of Dundee, Dow Street, Dundee DD1 5EH, Scotland - UK
(1)
Publication date
2019
(1)
2017
(1)
2023
(1)
First Public Date
2019
(1)
2017
(1)
Tags
xref:PubMed:30595439
(1)
Previous
page
1 / 5
You're on page
1
page
2
page
3
page
4
page
5
Next
page
Sort
by:
Relevance
Page size
10
Meier-Gorlin syndrome.
Not available
S-EPMC4574002
|
biostudies-literature
Cite
Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation.
Not available
S-EPMC8130261
|
biostudies-literature
Cite
Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
Not available
S-EPMC3068194
|
biostudies-literature
Cite
A Meier-Gorlin syndrome mutation impairs the ORC1-nucleosome association.
Not available
S-EPMC4654454
|
biostudies-literature
Cite
Novel Compound Heterozygous Variants in the
CDC6
Gene in a Russian Patient with Meier-Gorlin Syndrome.
Not available
S-EPMC8747802
|
biostudies-literature
Cite
Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.
Not available
S-EPMC9215265
|
biostudies-literature
Cite
Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype.
Not available
S-EPMC5886151
|
biostudies-literature
Cite
The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome.
Not available
S-EPMC10400559
|
biostudies-literature
Cite
Molecular impacts of Meier-Gorlin syndrome mutations on human origin licensing.
Not available
S-EPMC12830165
|
biostudies-literature
Cite
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
Not available
S-EPMC4678788
|
biostudies-literature
Cite
Previous
page
1 / 5
You're on page
1
page
2
page
3
page
4
page
5
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets
