OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Advanced
Search
59
Results
Show all
Save search
Copy query
Show results for
Unknown
(58)
Genomics
(1)
Organisms
Homo sapiens
(1)
Repository
EGA
(1)
Publication Date
Release Date
2018
(11)
2016
(10)
2019
(6)
2015
(6)
2017
(5)
2022
(4)
2025
(3)
2020
(3)
2024
(2)
2023
(2)
2021
(1)
2014
(1)
2013
(1)
2011
(1)
2010
(1)
2009
(1)
Previous
page
1 / 6
You're on page
1
page
2
page
3
page
4
page
5
page
6
Next
page
Sort
by:
Relevance
Page size
10
Intestinal Autophagy Improves Healthspan and Longevity in C. elegans during Dietary Restriction.
Not available
S-EPMC4945006
|
biostudies-literature
Cite
A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report.
Not available
S-EPMC5055717
|
biostudies-literature
Cite
C. elegans S6K Mutants Require a Creatine-Kinase-like Effector for Lifespan Extension.
Not available
S-EPMC4823261
|
biostudies-literature
Cite
Tumor immune microenvironment and genomic evolution in a patient with metastatic triple negative breast cancer and a complete response to atezolizumab.
Not available
S-EPMC6813065
|
biostudies-literature
Cite
Case report: Plasma cell leukemia secondary to multiple myeloma successfully treated with anti-BCMA CAR-T cell therapy.
Not available
S-EPMC9533140
|
biostudies-literature
Cite
Sequential Immunizations with Influenza Neuraminidase Protein Followed by Peptide Nanoclusters Induce Heterologous Protection.
Not available
S-EPMC10819419
|
biostudies-literature
Cite
Rapid Weight Loss and Severe Failure to Thrive Mimicking Lipodystrophy Syndrome in a 1-Year-Old Taiwanese Girl with Costello Syndrome.
Not available
S-EPMC9221830
|
biostudies-literature
Cite
Prenatal diagnosis of intellectual disability, autosomal dominant 29 with a nonsense pathogenic variant in <i>SETBP1</i>: a case report and literature review.
Not available
S-EPMC11936921
|
biostudies-literature
Cite
Managing primary open-angle glaucoma in the setting of suboptimal surgical outcomes in the fellow eye.
Not available
S-EPMC10688560
|
biostudies-literature
Cite
Novel Compound Heterozygous Mutations in
CRTAP
Cause Rare Autosomal Recessive Osteogenesis Imperfecta.
Not available
S-EPMC7457090
|
biostudies-literature
Cite
Previous
page
1 / 6
You're on page
1
page
2
page
3
page
4
page
5
page
6
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets