BAZ1B
MIM.605681 7q11-q21
Image Gallery
[ (
||image_reduire{0,60}|inserer_attribut{alt,WSTF (BAZ1B) and the control of gene expression by Vitamin D (...)})
]
Pathology
deleted in the Williams-Beuren syndrome (MIM.190450) deletion region.
Humpath.com - Human pathology - Photos - pictures - videos
||image_reduire{0,60}|inserer_attribut{alt,WSTF (BAZ1B) and the control of gene expression by Vitamin D (...)})
]
Sections
Keywords
- Agents
- Banner types
- Clinical
- Cytogenetics
- Disease
-
- Association (1)
- Disease (1038)
- Disease group (age related) (4)
- Disease group (etiology) (102)
- Disease group (localization) (32)
- Disease group (mechanisms) (29)
- Disease group (molecular) (30)
- Disease group (semiology) (15)
- Disease localization (137)
- Disease subtype (25)
- Group of diseases (191)
- Pediatric diseases (4)
- Diseases (Etiology)
-
- Allograft rejection (1)
- Chromosomal diseases (14)
- Complex disease (3)
- Drug-induced diseases (2)
- Environnemental diseases (1)
- Etiology unknown (3)
- Fungal diseases (1)
- Infectious diseases (106)
- Microdeletion syndrome (2)
- Monogenic disease (426)
- Multifactorial diseases (3)
- Multigenic disease (2)
- Parasitic disease (4)
- Senescence (3)
- Toxic diseases (1)
- Tumoral diseases (3)
- Unknown etiology (13)
- Viral diseases (3)
- General
-
- Administration (5)
- Biographies (14)
- Case studies (1)
- Companies (1)
- Concept (61)
- Contributors (1)
- En cours (10)
- Field (40)
- History (3)
- Journal (41)
- Macroscopy (3)
- Medical education (11)
- Pediatric pathology (4)
- Project (2)
- Resident course (7)
- Society (1)
- Student course (8)
- Synopsis (2)
- Technique (125)
- Terminology (1)
- Therapeutics (2)
- Website (10)
- Malformations
-
- Deformations (41)
- Developmental anomaly (4)
- Disruptions (2)
- Dysmorphology (54)
- Fetal anomalies (15)
- Malformation localization (1)
- Malformation subtype (5)
- Malformations (306)
- Malformative associations (19)
- Malformative disease (1)
- Malformative groups (80)
- Malformative lesions (19)
- Malformative sequences (6)
- Malformatives syndromes (38)
- Tissular malformations (36)
- Vascular malformations (3)
- Visceral malformations (33)
- Molecular
-
- amino acids (5)
- Carbohydrates (7)
- Chemical element (3)
- Developmental pathways (1)
- Genes (6)
- Genomic anomalies (3)
- Glycosaminoglycans (3)
- Ions (3)
- Lipids (17)
- Metabolic pathways (11)
- miRNAs (3)
- Molecualr anomalies (1)
- Molecular anatomy (1)
- Molecular complex (11)
- Molecular function (51)
- Molecular groups (93)
- Molecular lesions (9)
- Molecular medicine (41)
- Molecular processes (39)
- Molecular structure (5)
- Molecules (95)
- Nucleic acids (33)
- Proteoglycans (1)
- References (2)
- Signaling pathways (33)
- Morphological anomalies
-
- Artefact (1)
- Cellular anomalies (7)
- Cellular lesions (35)
- Cyst (1)
- Lesional group (108)
- Lesional syndrome (416)
- Macroscopical anomaly (49)
- Macroscopical lesions (296)
- Macroscopical syndromes (14)
- Microscopical anomaly (2)
- Microscopical lesions (230)
- Pathogenesis (1)
- Pathological cells (8)
- Pathological processes (46)
- Procedures (1)
- Tissular anomaly (25)
- Tissular lesions (134)
- Ultrastructural lesions (5)
- Pathological groups
- Physiological
-
- Anatomical component (76)
- Cell subtype (1)
- Cell subtypes (24)
- Cells (84)
- Cellular components (100)
- Cellular functions (88)
- Cellular groups (14)
- Cellular processes (26)
- Cellular systems (4)
- Chromosomal regions (9)
- Chromosomes (3)
- Developmental processes (82)
- Developmental structures (32)
- Fetal organs (48)
- Individuals (2)
- Organ components (98)
- Organ functions (8)
- Organs (48)
- Regions (12)
- System component (3)
- Systemic functions (15)
- Systemic processes (1)
- Systems (13)
- Tissues (9)
- Tissular components (111)
- Tissular functions (23)
- Tissular processes (3)
- Physiopathological pathways
-
- Atopia - Allergy (1)
- Autoimmune diseases (8)
- Connective tissue diseases (1)
- Dysfunctional diseases (15)
- Dysimmune diseases (26)
- Endocrine disease (6)
- Immunodeficiency (31)
- Infection predisposition (1)
- Inflammatory diseases (13)
- Malformative diseases (75)
- Metabolic disease (112)
- Neurodegenerative disease (8)
- Toxic diseases (4)
- Tumoral diseases (13)
- Tumoral predisposition (14)
- Vascular diseases (8)
- Proteins
-
- Activated in tumors (7)
- Amplified in tumors (25)
- Autoimmunity targets (8)
- Biomarkers (1)
- Cancer gene (123)
- CDs (16)
- Deleted in human disease (1)
- Diagnostic antibodies (2)
- Druggable (2)
- Functional proteic groups (45)
- Fusion proteins (50)
- Human evolution (2)
- Hypermethylated in tumors (1)
- IHC marker (30)
- Inactivated in tumors (14)
- Involved in translocations (137)
- Malformation genes (38)
- Mutant protein (4)
- Mutated in human diseases (602)
- Mutated in tumors (20)
- Overexpressed in tumors (38)
- Proteic complexes (64)
- Proteic domains (2)
- Protein family (304)
- Protein groups (56)
- Protein subfamily (3)
- Protein superfamilies (62)
- Proteins (1516)
- Putative cancer genes (3)
- Tumor suppressor protein (47)
- Underexpressed in tumors (5)
- Variants in disease predisposition (51)
- Therapeutics
- Tumors
-
- Architectural pattern (16)
- Benign tumors (7)
- Carcinomas (12)
- Cytological pattern (4)
- Leukemias (13)
- Lymphomas (2)
- Malignant tumors (10)
- Multigenic tumorigenesis (3)
- Orphan tumors (15)
- Pediatric tumors (17)
- Rare tumors (1)
- Sarcomas (3)
- Sof tissue tumor (23)
- Translocation-associated tumors (24)
- Tumor (570)
- Tumoral cells (5)
- Tumoral groups (272)
- Tumoral localization (234)
- Tumoral subtypes (198)
- Videos
Copyright humpath.com, website in human pathology | Web design by PBCom.net