X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2770) 2770
Book Review (567) 567
Publication (186) 186
Newsletter (84) 84
Book Chapter (24) 24
Conference Proceeding (5) 5
Dissertation (5) 5
Magazine Article (3) 3
Reference (3) 3
Book / eBook (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (2389) 2389
humans (2365) 2365
male (1295) 1295
agammaglobulinemia - genetics (1146) 1146
x-linked agammaglobulinemia (913) 913
female (898) 898
immunology (799) 799
agammaglobulinemia (671) 671
child (620) 620
adult (588) 588
animals (566) 566
agammaglobulinemia - immunology (559) 559
abridged index medicus (511) 511
agammaglobulinemia - complications (460) 460
child, preschool (455) 455
mutation (449) 449
protein-tyrosine kinases - genetics (445) 445
infant (439) 439
adolescent (419) 419
x chromosome (393) 393
mice (369) 369
b-lymphocytes - immunology (338) 338
immunodeficiency (329) 329
genetic linkage (326) 326
agammaglobulinemia - diagnosis (289) 289
common variable immunodeficiency (284) 284
middle aged (259) 259
immunologic deficiency syndromes - genetics (252) 252
molecular sequence data (238) 238
expression (223) 223
protein-tyrosine kinases - metabolism (219) 219
brutons tyrosine kinase (210) 210
genetics & heredity (207) 207
hypogammaglobulinemia (204) 204
immunologic deficiency syndromes - immunology (200) 200
allergy (197) 197
agammaglobulinemia - therapy (195) 195
pediatrics (195) 195
biochemistry & molecular biology (190) 190
pedigree (190) 190
research (188) 188
immunoglobulins (178) 178
gene (175) 175
t-lymphocytes - immunology (169) 169
btk (168) 168
base sequence (166) 166
genetic aspects (166) 166
phenotype (166) 166
lymphocytes (163) 163
signal transduction (162) 162
hematology (156) 156
amino acid sequence (155) 155
activation (146) 146
b cells (145) 145
infectious diseases (141) 141
infant, newborn (135) 135
agammaglobulinemia - pathology (131) 131
disease (131) 131
bruton's tyrosine kinase (129) 129
genetic diseases, x-linked - genetics (129) 129
infections (129) 129
mutations (125) 125
aged (123) 123
internal medicine (121) 121
allergy and immunology (118) 118
analysis (118) 118
health aspects (118) 118
medicine, general & internal (117) 117
phosphorylation (115) 115
cell differentiation (114) 114
proteins (114) 114
severe combined immunodeficiency (112) 112
agammaglobulinemia - etiology (109) 109
agammaglobulinaemia tyrosine kinase (108) 108
genes (107) 107
protein-tyrosine kinases - chemistry (107) 107
children (106) 106
immunoglobulins, intravenous - therapeutic use (106) 106
agammaglobulinemia - drug therapy (105) 105
polymerase chain reaction (104) 104
tyrosine (104) 104
cell biology (103) 103
immunologic deficiency syndromes - diagnosis (103) 103
tyrosine kinase (103) 103
agammaglobulinemia - blood (102) 102
care and treatment (101) 101
common variable immunodeficiency - immunology (101) 101
agammaglobulinemia - enzymology (100) 100
deficiency (100) 100
syndrome (100) 100
medicine, research & experimental (98) 98
patients (98) 98
diagnosis (97) 97
young adult (97) 97
cell line (95) 95
genetic diseases, x-linked - complications (95) 95
antibodies (94) 94
primary immunodeficiency (93) 93
t-cells (93) 93
antibody formation (92) 92
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2646) 2646
French (65) 65
German (39) 39
Japanese (36) 36
Spanish (21) 21
Italian (12) 12
Chinese (10) 10
Dutch (10) 10
Polish (8) 8
Russian (6) 6
Czech (5) 5
Hungarian (4) 4
Korean (4) 4
Portuguese (3) 3
Romanian (3) 3
Norwegian (2) 2
Swedish (2) 2
Danish (1) 1
Finnish (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 06/2012, Volume 90, Issue 6, pp. 986 - 1001
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2015, Volume 136, Issue 4, pp. 993 - 1006.e1
Journal Article
Nature Medicine, ISSN 1078-8956, 12/2014, Volume 20, Issue 12, pp. 1410 - 1416
The protein cytotoxic T lymphocyte antigen-4 (CTLA-4) is an essential negative regulator of immune responses, and its loss causes fatal autoimmunity in mice.... 
PATHWAYS | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICAL-PICTURE | HOMEOSTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | AUTOIMMUNITY | REGULATORY T-CELLS | GERMLINE MUTATIONS | MICE | BLOCKADE | IMMUNODEFICIENCY | ABATACEPT | Recurrence | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Purpura, Thrombocytopenic, Idiopathic - genetics | Exons | Immune System Diseases - genetics | Humans | Middle Aged | Male | Anemia, Hemolytic, Autoimmune - genetics | Mutation, Missense | Respiratory Tract Infections - genetics | T-Lymphocytes, Regulatory - immunology | Autoimmune Diseases - genetics | Young Adult | Purpura, Thrombocytopenic, Idiopathic - immunology | Adult | Female | Endocytosis - genetics | Polyendocrinopathies, Autoimmune - genetics | Child | Endocytosis - immunology | Granuloma - genetics | Autoimmune Diseases - immunology | CTLA-4 Antigen - genetics | B7-1 Antigen - metabolism | Codon, Nonsense | CTLA-4 Antigen - immunology | Syndrome | Polyendocrinopathies, Autoimmune - immunology | Lung Diseases, Interstitial - immunology | Animals | B-Lymphocytes - immunology | Lung Diseases, Interstitial - genetics | Pedigree | Anemia, Hemolytic, Autoimmune - immunology | Adolescent | Respiratory Tract Infections - immunology | Granuloma - immunology | Heterozygote | Mice | Antigens | Gene mutations | Physiological aspects | Genetic aspects | Immunologic diseases | Research | Risk factors | Proteins | Homeostasis | Cytotoxicity | Ligands | T cell receptors | Mutation | Immune system | Index Medicus
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 4/2016, Volume 36, Issue 3, pp. 187 - 194
X-linked agammagobulinemia (XLA) is a primary immunodeficiency caused by Bruton’s tyrosine kinase (BTK) gene defect. XLA patients have absent or reduced number... 
Medical Microbiology | north african population | Biomedicine | Immunology | novel mutations | BTK | Infectious Diseases | Internal Medicine | XLA | GENOTYPE-PHENOTYPE CORRELATION | GENE-MUTATIONS | GENOMIC ORGANIZATION | IMMUNOLOGY | IDENTIFICATION | B-CELLS | BRUTONS TYROSINE KINASE | FAMILIES | AGAMMAGLOBULINEMIA XLA | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Humans | Child, Preschool | Genetic Diseases, X-Linked - complications | Agammaglobulinemia - diagnosis | Infant | Male | Genetic Counseling | Protein-Tyrosine Kinases - immunology | Protein-Tyrosine Kinases - genetics | Morocco | Adult | Genetic Diseases, X-Linked - genetics | Algeria | Opportunistic Infections - immunology | B-Lymphocytes - pathology | Child | Tunisia | Opportunistic Infections - complications | Gene Expression | Agammaglobulinemia - complications | Genetic Association Studies | Gene Frequency | Opportunistic Infections - genetics | Sequence Analysis, DNA | Genetic Diseases, X-Linked - diagnosis | Opportunistic Infections - diagnosis | Genetic Diseases, X-Linked - immunology | B-Lymphocytes - immunology | Age of Onset | Alleles | Heterozygote | Mutation | Genetic research | Genetic aspects | B cells | Index Medicus | Agammaglobulinemia/diagnosis | Protein-Tyrosine Kinases/genetics | Agammaglobulinemia/complications | Life Sciences | Agammaglobulinemia/genetics | Genetic Diseases, X-Linked/complications | Opportunistic Infections/complications | Biochemistry, Molecular Biology | Agammaglobulinemia/immunology | Genetic Diseases, X-Linked/immunology | B-Lymphocytes/pathology | Genetic Diseases, X-Linked/diagnosis | Opportunistic Infections/diagnosis | B-Lymphocytes/immunology | Protein-Tyrosine Kinases/immunology | Agammaglobulinaemia Tyrosine Kinase | Opportunistic Infections/immunology | Opportunistic Infections/genetics | Genetic Diseases, X-Linked/genetics
Journal Article
Scandinavian Journal of Gastroenterology, ISSN 0036-5521, 06/2013, Volume 48, Issue 6, pp. 672 - 678
Abstract Objective. Early-onset colorectal cancer (CRC), defined here as age of onset less than 40 years, develops frequently in genetically predisposed... 
mutation | exome | genetic predisposition to disease | colorectal neoplasms | age of onset | Exome | Genetic predisposition to disease | Colorectal neoplasms | Mutation | Age of onset | MOLECULAR-FEATURES | LYNCH-SYNDROME | MICROSATELLITE INSTABILITY | GUIDELINES | X-LINKED AGAMMAGLOBULINEMIA | AMERICAN-COLLEGE | COLON | GASTROENTEROLOGY & HEPATOLOGY | CARCINOMA | GENETIC ALTERATIONS | AGE | MutL Protein Homolog 1 | Microsatellite Instability | Genetic Testing | Humans | DNA Repair Enzymes - genetics | Male | Intestinal Polyposis - diagnosis | Young Adult | Intestinal Polyposis - congenital | Smad4 Protein - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Adult | Female | Mismatch Repair Endonuclease PMS2 | Neoplastic Syndromes, Hereditary - genetics | Adenomatous Polyposis Coli - genetics | Nuclear Proteins - genetics | Adenomatous Polyposis Coli Protein - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Intestinal Polyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | DNA Glycosylases - genetics | Protein-Serine-Threonine Kinases - genetics | Bone Morphogenetic Protein Receptors, Type I - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Sequence Analysis, DNA | Exome - genetics | Adaptor Proteins, Signal Transducing - genetics | Adenosine Triphosphatases - genetics | Adenomatous Polyposis Coli - diagnosis | Index Medicus
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2011, Volume 129, Issue 3, pp. 801 - 810.e6
Background Complement receptor 2 (CR2/CD21) is part of the B-cell coreceptor and expressed by mature B cells and follicular dendritic cells. CD21 is a receptor... 
Allergy and Immunology | B lymphocyte | hypogammaglobulinemia | common variable immunodeficiency | complement receptor | CD21 | COMPLEMENT RECEPTOR TYPE-2 | CR-2 | IMMUNOLOGY | PNEUMOCOCCAL POLYSACCHARIDES | LYMPHOCYTE-B RECEPTOR | CAPSULAR POLYSACCHARIDE | ALLERGY | C3D | FOLLICULAR DENDRITIC CELLS | ANTIBODY-RESPONSE | EPSTEIN-BARR-VIRUS | Agammaglobulinemia - immunology | Protein Binding - genetics | Agammaglobulinemia - genetics | Humans | Receptors, Complement 3d - immunology | Agammaglobulinemia - diagnosis | Male | Infection - etiology | Complement C3d - metabolism | DNA Mutational Analysis | Receptors, Complement 3d - genetics | Infection - diagnosis | HEK293 Cells | Adult | Viral Matrix Proteins - metabolism | Antigen-Antibody Complex - metabolism | B-Lymphocytes - pathology | B-Lymphocytes - metabolism | Immunologic Memory - genetics | Agammaglobulinemia - complications | Infection - immunology | Immunity, Humoral - genetics | Transgenes - genetics | Infection - genetics | B-Lymphocytes - immunology | Receptors, Complement 3d - metabolism | Calcium Signaling - genetics | Sequence Deletion - genetics | Viral antibodies | Polysaccharides | Goats | Dendritic cells | Antibodies | Genetic research | Genetic aspects | Universities and colleges | Flow cytometry | Cloning | Kinases | Gene expression | Defects | Proteins | Hepatitis | Cell growth | Mutagenesis | Ligands | Mutation | Tetanus | Autoimmune diseases | Immune system | Index Medicus | Abridged Index Medicus
Journal Article
Blood, ISSN 0006-4971, 05/2017, Volume 129, Issue 19, pp. 2624 - 2635
Journal Article
Clinical Immunology, ISSN 1521-6616, 2017, Volume 176, pp. 77 - 86
Journal Article
Blood, ISSN 0006-4971, 01/2015, Volume 125, Issue 4, pp. 639 - 648
The signal transducer and activator of transcription (STAT) family of transcription factors orchestrate hematopoietic cell differentiation. Recently, mutations... 
HYPER-IGE SYNDROME | IMMUNE DYSREGULATION | ENTEROPATHY | GRANULAR LYMPHOCYTIC-LEUKEMIA | DISORDERS | POLYENDOCRINOPATHY | GENERATION | HEMATOLOGY | CHRONIC MUCOCUTANEOUS CANDIDIASIS | T-CELLS | DEFICIENCY | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Dendritic Cells - immunology | Humans | Genetic Diseases, Inborn - genetics | Dendritic Cells - pathology | Killer Cells, Natural - pathology | Genetic Diseases, Inborn - pathology | Mutation, Missense | Mycobacterium Infections - immunology | T-Lymphocytes, Regulatory - pathology | T-Lymphocytes, Regulatory - immunology | Autoimmune Diseases - genetics | Cell Differentiation - genetics | Agammaglobulinemia - pathology | Mycobacterium Infections - genetics | Killer Cells, Natural - immunology | Adult | Female | Mycobacterium Infections - pathology | Leukemia, Large Granular Lymphocytic - pathology | B-Lymphocytes - pathology | Leukemia, Large Granular Lymphocytic - immunology | Autoimmune Diseases - pathology | STAT3 Transcription Factor - genetics | Th17 Cells - pathology | Protein Structure, Tertiary | Autoimmune Diseases - immunology | Genetic Diseases, Inborn - immunology | Cell Differentiation - immunology | B-Lymphocytes - immunology | Adolescent | Th17 Cells - immunology | STAT3 Transcription Factor - immunology | Amino Acid Substitution | Leukemia, Large Granular Lymphocytic - genetics | Index Medicus | Abridged Index Medicus | Immunobiology
Journal Article
PLoS Genetics, ISSN 1553-7390, 10/2017, Volume 13, Issue 10, pp. e1007050 - e1007050
Journal Article