OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Advanced
Search
23
Results
Show all
Save search
Copy query
Show results for
Unknown
(23)
Publication Date
Release Date
2021
(6)
2022
(4)
2014
(3)
2024
(2)
2020
(2)
2023
(1)
2018
(1)
2017
(1)
2016
(1)
2015
(1)
2004
(1)
Previous
page
1 / 3
You're on page
1
page
2
page
3
Next
page
Sort
by:
Relevance
Page size
10
Longitudinal analysis of CD8+ T cells specific for structural and nonstructural hepatitis B virus proteins in patients with chronic hepatitis B: implications for immunotherapy.
Not available
S-EPMC415806
|
biostudies-literature
Cite
Combination of cycle threshold time, absolute lymphocyte count and neutrophil:lymphocyte ratio is predictive of hypoxia in patients with SARS-CoV-2 infection.
Not available
S-EPMC8754692
|
biostudies-literature
Cite
Postdischarge outcomes of COVID-19 patients from South Asia: a prospective study.
Not available
S-EPMC9129199
|
biostudies-literature
Cite
Innate immunity. A Spaetzle-like role for nerve growth factor β in vertebrate immunity to Staphylococcus aureus.
Not available
S-EPMC4255479
|
biostudies-literature
Cite
Estimating the Risk of Severe Peanut Allergy Using Clinical Background and IgE Sensitization Profiles.
Not available
S-EPMC8974676
|
biostudies-literature
Cite
Safety and immunogenicity of concomitant administration of COVID-19 vaccines (ChAdOx1 or BNT162b2) with seasonal influenza vaccines in adults in the UK (ComFluCOV): a multicentre, randomised, controlled, phase 4 trial.
Not available
S-EPMC8585490
|
biostudies-literature
Cite
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation.
Not available
S-EPMC5374029
|
biostudies-literature
Cite
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
Not available
S-EPMC6148345
|
biostudies-literature
Cite
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Not available
S-EPMC8246418
|
biostudies-literature
Cite
Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Not available
S-EPMC7334047
|
biostudies-literature
Cite
Previous
page
1 / 3
You're on page
1
page
2
page
3
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets