OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Advanced
Search
49
Results
Show all
Save search
Copy query
Show results for
Unknown
(49)
Publication Date
Release Date
2024
(7)
2021
(7)
2023
(6)
2022
(6)
2020
(5)
2025
(3)
2016
(3)
2015
(3)
2026
(2)
2018
(2)
2019
(1)
2014
(1)
2013
(1)
2011
(1)
2009
(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
Modification of perpendicular magnetic anisotropy and domain wall velocity in Pt/Co/Pt by voltage-induced strain.
Not available
S-EPMC4300497
|
biostudies-literature
Cite
Current-Induced Domain Wall Motion and Tilting in Perpendicularly Magnetized Racetracks.
Not available
S-EPMC6093834
|
biostudies-literature
Cite
Observation of a phase transition within the domain walls of ferromagnetic Co
3
Sn
2
S
2
.
Not available
S-EPMC9151713
|
biostudies-literature
Cite
Magneto-optical imaging of thin magnetic films using spins in diamond.
Not available
S-EPMC4789603
|
biostudies-literature
Cite
Public and Patient Involvement in Doctoral Research During the COVID-19 Pandemic: Reflections on the Process, Challenges, Impact and Experiences From the Perspectives of Adults With Cerebral Palsy and the Doctoral Researcher.
Not available
S-EPMC9397843
|
biostudies-literature
Cite
An Artificial Intelligence Characterised Functional Ingredient, Derived from Rice, Inhibits TNF-α and Significantly Improves Physical Strength in an Inflammaging Population.
Not available
S-EPMC7555431
|
biostudies-literature
Cite
Randomised controlled trial to investigate the effectiveness of thoracic epidural and paravertebral blockade in reducing chronic post-thoracotomy pain (TOPIC): a pilot study to assess feasibility of a large multicentre trial.
Not available
S-EPMC6624049
|
biostudies-literature
Cite
Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study.
Not available
S-EPMC11790076
|
biostudies-literature
Cite
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.
Not available
S-EPMC3724403
|
biostudies-literature
Cite
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.
Not available
S-EPMC3404892
|
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
