X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
female (7) 7
humans (7) 7
index medicus (7) 7
mutation (6) 6
child (5) 5
male (4) 4
child, preschool (3) 3
diagnosis (3) 3
hematopoietic stem cell transplantation (3) 3
hematopoietic stem cells (3) 3
immunodeficiency (3) 3
immunology (3) 3
infant (3) 3
internal medicine (3) 3
patients (3) 3
b-cells (2) 2
biomedicine (2) 2
children (2) 2
consanguinity (2) 2
diarrhea (2) 2
diseases (2) 2
hematology (2) 2
infections (2) 2
infectious diseases (2) 2
medical microbiology (2) 2
mutations (2) 2
pancytopenia (2) 2
phenotype (2) 2
stem cell transplantation (2) 2
transplantation (2) 2
yeast (2) 2
abridged index medicus (1) 1
adhesion (1) 1
adolescent (1) 1
adult (1) 1
agammaglobulinemia - genetics (1) 1
agammaglobulinemia - immunology (1) 1
agammaglobulinemia - pathology (1) 1
agammaglobulinemia - therapy (1) 1
age (1) 1
aged (1) 1
aids-related opportunistic infections (1) 1
aids/hiv (1) 1
algorithms (1) 1
allergology (1) 1
anemia (1) 1
article (1) 1
ataxia telangiectasia - pathology (1) 1
ataxia telangiectasia - virology (1) 1
ataxia-telangiectasia (1) 1
atm (1) 1
atypical scid (1) 1
autosomal recessive forms (1) 1
b-lymphocytes - immunology (1) 1
bacterial infections - microbiology (1) 1
biological response modifiers (1) 1
biomarkers (1) 1
biosynthesis (1) 1
bleeding (1) 1
blood (1) 1
blood groups (1) 1
bone and bones - abnormalities (1) 1
bone marrow diseases - complications (1) 1
bone marrow diseases - enzymology (1) 1
bone marrow diseases - genetics (1) 1
bone marrow diseases - physiopathology (1) 1
cardiomyopathies - virology (1) 1
case-control studies (1) 1
cd11a (1) 1
cd11a antigen (1) 1
cd18 (1) 1
cd18 antigen (1) 1
cd18 antigens - genetics (1) 1
cd18 antigens - metabolism (1) 1
cd4 antigen (1) 1
cell activation (1) 1
cell surface (1) 1
cell survival (1) 1
cell-differentiation (1) 1
central-nervous-system (1) 1
chromosomes, human, x - genetics (1) 1
circular dichroism (1) 1
clinical and immunological phenotype (1) 1
clinical-features (1) 1
clonal deletion (1) 1
colorimetry (1) 1
common gamma chain (1) 1
constipation (1) 1
cytokines (1) 1
cytoplasm (1) 1
deficiency (1) 1
deletion (1) 1
development and progression (1) 1
discovery (1) 1
disease (1) 1
disease susceptibility (1) 1
disorders (1) 1
dominant (1) 1
eif6 release (1) 1
enzymes (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


European Journal of Clinical Investigation, ISSN 0014-2972, 02/2019, Volume 49, Issue 2, pp. e13047 - n/a
Journal Article
American Journal of Hematology, ISSN 0361-8609, 01/2017, Volume 92, Issue 1, pp. 28 - 36
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/2017, Volume 54, Issue 8, pp. 558 - 566
Journal Article
European Journal of Clinical Investigation, ISSN 0014-2972, 02/2019, Volume 49, Issue 2, p. e13047
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/2017, Volume 54, Issue 8, pp. 558 - 566
Background For the final step of the maturation of the ribosome, the nascent 40S and 60S subunits are exported from the nucleus to the cell cytoplasm. To... 
YEAST | DIAGNOSIS | EIF6 RELEASE | GENETICS & HEREDITY | GUANINE-NUCLEOTIDE EXCHANGE | SYNDROME PROTEIN | SACCHAROMYCES-CEREVISIAE | GTPASE | RIBOSOME | SUBUNIT | Genetic aspects | Research | Gene mutations | Pancytopenia
Journal Article
ISSN 1468-6244, 2017
For the final step of the maturation of the ribosome, the nascent 40S and 60S subunits are exported from the nucleus to the cell cytoplasm. To prevent... 
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 11/2014, Volume 34, Issue 8, pp. 904 - 909
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 11/2014, Volume 34, Issue 8, p. 904
  Interferon-γ receptor 2 (IFN-γR2) deficiency is a rare primary immunodeficiency characterized by predisposition to infections with weakly virulent... 
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 11/2014, Volume 34, Issue 8, p. 904
Interferon-I[sup.3] receptor 2 (IFN-I[sup.3]R2) deficiency is a rare primary immunodeficiency characterized by predisposition to infections with weakly... 
Immunodeficiency | Interferon | Virulence (Microbiology) | Biological response modifiers | Health aspects
Journal Article
Southern Medical Journal, ISSN 0038-4348, 10/1998, Volume 91, Issue Supplement, p. S9
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.