OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Advanced
Search
89
Results
Show all
Save search
Copy query
Show results for
Unknown
(76)
Genomics
(13)
Organisms
Homo sapiens
(13)
Repository
EGA
(13)
Technology Type
Illumina 15K
(8)
Publication Date
Release Date
2022
(9)
2021
(8)
2018
(7)
2019
(6)
2024
(5)
2023
(5)
2009
(5)
2020
(4)
2012
(4)
2008
(4)
2017
(3)
2016
(3)
2014
(3)
2007
(3)
2025
(2)
2010
(2)
2015
(1)
2013
(1)
2011
(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
Revertant mosaic fibroblasts in recessive dystrophic epidermolysis bullosa.
Not available
S-EPMC6766431
|
biostudies-literature
Cite
CRISPR/Cas9-based genetic correction for recessive dystrophic epidermolysis bullosa.
Not available
S-EPMC5328670
|
biostudies-literature
Cite
Patient-specific naturally gene-reverted induced pluripotent stem cells in recessive dystrophic epidermolysis bullosa.
Not available
S-EPMC3989384
|
biostudies-literature
Cite
Rapid generation of Col7a1
-/-
mouse model of recessive dystrophic epidermolysis bullosa and partial rescue via immunosuppressive dermal mesenchymal stem cells.
Not available
S-EPMC5623156
|
biostudies-literature
Cite
Evaluation of intestinal biopsy tissue preservation methods to facilitate large-scale mucosal microbiota research.
Not available
S-EPMC11751561
|
biostudies-literature
Cite
The impact of psychiatric comorbidity on Parkinson's disease outcomes: a systematic review and meta-analysis.
Not available
S-EPMC10867667
|
biostudies-literature
Cite
Stroke Outcome Related to Initial Volume Status and Diuretic Use.
Not available
S-EPMC9798788
|
biostudies-literature
Cite
Dopamine and Glutamate in Antipsychotic-Responsive Compared With Antipsychotic-Nonresponsive Psychosis: A Multicenter Positron Emission Tomography and Magnetic Resonance Spectroscopy Study (STRATA).
Not available
S-EPMC7965076
|
biostudies-literature
Cite
Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration.
Not available
S-EPMC5294887
|
biostudies-literature
Cite
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures.
Not available
S-EPMC6037130
|
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