X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (54) 54
humans (50) 50
hax1 (43) 43
neutropenia - genetics (36) 36
neutropenia - congenital (35) 35
severe congenital neutropenia (35) 35
male (26) 26
mutation (26) 26
female (25) 25
neutropenia (23) 23
adaptor proteins, signal transducing - genetics (20) 20
hematology (19) 19
child (18) 18
elastase (18) 18
genetic disorders (18) 18
deficiency (16) 16
infant (16) 16
disease (15) 15
adaptor proteins, signal transducing (14) 14
ela2 (14) 14
immunology (14) 14
pediatrics (14) 14
proteins - genetics (13) 13
apoptosis (12) 12
genetic aspects (12) 12
hax1 mutations (12) 12
gene (11) 11
leukemia (11) 11
mutations (10) 10
neutropenia - diagnosis (10) 10
neutropenia - pathology (10) 10
phenotype (10) 10
adolescent (9) 9
adult (9) 9
child, preschool (9) 9
granulocyte colony-stimulating factor - therapeutic use (9) 9
pedigree (9) 9
analysis (8) 8
animals (8) 8
biochemistry & molecular biology (8) 8
cell biology (8) 8
genetic research (8) 8
infantile genetic agranulocytosis (8) 8
leukocyte elastase - genetics (8) 8
neutropenia - complications (8) 8
unfolded protein response (8) 8
children (7) 7
gene mutations (7) 7
gfi1 (7) 7
hax1 gene (7) 7
original kostmann family (7) 7
adaptor proteins, signal transducing - metabolism (6) 6
bacterial infections (6) 6
consanguinity (6) 6
cyclic neutropenia (6) 6
diagnosis (6) 6
dna mutational analysis (6) 6
glucose-6-phosphatase - genetics (6) 6
mice (6) 6
neutropenia - therapy (6) 6
neutrophils - pathology (6) 6
oncology (6) 6
serine endopeptidases - genetics (6) 6
biomedicine (5) 5
cancer (5) 5
cell line (5) 5
colony-stimulating factor (5) 5
csf3r mutations (5) 5
elane (5) 5
family (5) 5
g6pc3 (5) 5
genotype (5) 5
health aspects (5) 5
hematopoietic stem cells (5) 5
infection (5) 5
iranian patients (5) 5
kostmann (5) 5
neutrophils (5) 5
neutrophils - metabolism (5) 5
siblings (5) 5
allergy (4) 4
article (4) 4
congenital neutropenia (4) 4
developmental disabilities - genetics (4) 4
expression (4) 4
genetics & heredity (4) 4
granulocyte colony-stimulating factor (4) 4
hax (4) 4
hax-1 (4) 4
homozygote (4) 4
immunodeficiency (4) 4
immunologic deficiency syndromes - genetics (4) 4
infectious diseases (4) 4
internal medicine (4) 4
kostmann disease (4) 4
medicine & public health (4) 4
mitochondria (4) 4
mitochondrial proteins - metabolism (4) 4
mutation - genetics (4) 4
myeloid progenitor cells (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


F1000Research, ISSN 2046-1402, 08/2015, Volume 4, pp. 148 - 148
HS1-associated protein X-1 (Hax1) is a 35 kDa protein that is ubiquitously expressed. Hax1 is an anti-apoptotic protein with additional roles in cell motility,... 
Immune Response
Journal Article
Journal Article
Journal Article
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 2/2017, Volume 37, Issue 2, pp. 117 - 122
Severe congenital neutropenia (SCN), originally described by the Swedish pediatrician Rolf Kostmann, constitutes a heterogeneous disorder associated with a... 
Medical Microbiology | HAX1 | Immunology | Biomedicine | Kostmann’s disease | Internal Medicine | Infectious Diseases | Severe congenital neutropenia (SCN)
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 01/2015, Volume 62, Issue 1, pp. 103 - 108
Journal Article