OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Help
Advanced
Search
87
Results
Show all
Save search
Copy query
Show results for
Unknown
(86)
Proteomics
(1)
Organisms
Orthohepacivirus
(1)
Methylomicrobium album BG8
(1)
Crenomytilus
(1)
Severe acute respiratory syndrome coronavirus
(1)
Plasmodium sp. F
(1)
Roseburia inulinivorans DSM 16841
(1)
Bifidobacterium adolescentis ATCC 15703
(1)
Murine norovirus 1
(1)
Roseburia hominis A2-183
(1)
Aspergillus nidulans TN02A3
(1)
Aureobasidium pullulans EXF-150
(1)
Pyricularia oryzae B157
(1)
Fusarium graminearum GZ3639
(1)
Paramoeba perurans
(1)
Streptococcus pneumoniae SP14-BS69
(1)
Pseudomonas entomophila L48
(1)
Streptococcus equi subsp. equi 4047
(1)
Lactobacillus johnsonii N6.2
(1)
Saccharomyces cerevisiae S228
(1)
NEWT:723287
(1)
Naja mandalayensis
(1)
Vespa velutina nigrithorax
(1)
Burkholderia sp. 2332
(1)
Bacillus thuringiensis str. Al Hakam
(1)
Mycobacterium avium subsp. paratuberculosis K-10
(1)
Plasmodium sp. pBT9
(1)
Hendra virus horse/Australia/Hendra/1994
(1)
Porphyrobacter sp. WLSH-3
(1)
Actinomycetes
(1)
Acanthoscurria
(1)
Repository
pride
(1)
Tissue
Blood cell
(1)
Cell culture
(1)
Disease
Chronic myeloid leukemia
(1)
Technology Type
Bottom-up proteomics
(1)
Mass Spectrometry
(1)
Publication Date
2024
(1)
Release Date
2022
(9)
2021
(9)
2020
(7)
2016
(7)
2019
(6)
2023
(5)
2018
(5)
2017
(5)
2015
(5)
2024
(4)
2009
(4)
2025
(3)
2014
(3)
2013
(3)
2010
(2)
2006
(2)
2001
(2)
2000
(2)
2012
(1)
2011
(1)
2007
(1)
Lab affiliation
de Duve Institute UCLouvain and WELBIO
(1)
Previous
page
1 / 9
You're on page
1
page
2
page
3
page
4
page
5
page
...
page
9
Next
page
Sort
by:
Relevance
Page size
10
Clinical utility gene card for: ALG1 defective congenital disorder of glycosylation.
Not available
S-EPMC4592101
|
biostudies-literature
Cite
Clinical utility gene card for: Peters plus syndrome.
Not available
S-EPMC4970696
|
biostudies-literature
Cite
Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylation.
Not available
S-EPMC6871091
|
biostudies-literature
Cite
SRD5A3 defective congenital disorder of glycosylation: clinical utility gene card.
Not available
S-EPMC7609305
|
biostudies-literature
Cite
Clinical Utility Gene Card For: GALNT3 defective congenital disorder of glycosylation.
Not available
S-EPMC6057978
|
biostudies-literature
Cite
Clinical utility gene card for: DPAGT1 defective congenital disorder of glycosylation.
Not available
S-EPMC4795212
|
biostudies-literature
Cite
Clinical utility gene card for: Phosphomannomutase 2 deficiency.
Not available
S-EPMC4350603
|
biostudies-literature
Cite
Clinical utility gene card for: B4GALT7-defective congenital disorder of glycosylation.
Not available
S-EPMC5255951
|
biostudies-literature
Cite
Clinical utility gene card for: ALG6 defective congenital disorder of glycosylation.
Not available
S-EPMC4297893
|
biostudies-literature
Cite
Clinical utility gene card for: Phosphomannose isomerase deficiency.
Not available
S-EPMC4135420
|
biostudies-literature
Cite
Previous
page
1 / 9
You're on page
1
page
2
page
3
page
4
page
5
page
...
page
9
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets
