Diseases Associated With Protein Localization To Nucleus
| Disease |
|
Prostatic Neoplasms
|
|
Craniofacial Abnormalities
|
|
Diabetes Mellitus, Type 2
|
|
Breast Carcinoma
|
|
Hepatocellular Carcinoma
|
|
Leukemia, Promyelocytic, Acute
|
|
Cell Transformation, Neoplastic
|
|
Muscular Dystrophies, Limb-Girdle
|
|
Stomach Neoplasms
|
|
Muscular Dystrophy, Emery-Dreifuss
|
|
Myocardial Ischemia
|
|
Neoplasm Invasiveness
|
|
Liver Cirrhosis, Experimental
|
|
Left Ventricular Hypertrophy
|
|
Precancerous Conditions
|
|
Hiv Infections
|
|
Colorectal Cancer
|
|
Hand Deformities, Congenital
|
|
Campomelic Dysplasia
|
|
Carcinoma
|
|
Basal Cell Carcinoma
|
|
Carcinoma, Non-Small-Cell Lung
|
|
Renal Cell Carcinoma
|
|
Dilated Cardiomyopathy
|
|
Charcot-Marie-Tooth Disease, Type 2b1
|
|
Cholangitis
|
|
Coloboma
|
|
Congenital Abnormalities
|
|
Corneal Dystrophy, Fleck
|
|
Coronary Artery Disease
|
|
Deafness, Autosomal Dominant 23
|
|
Sudden Cardiac Arrest
|
|
Diabetes Mellitus
|
|
Diabetes Mellitus, Experimental
|
|
Diamond-Blackfan Anemia 7
|
|
Disease Progression
|
|
Limb Dystonia
|
|
Dystonia Musculorum Deformans Type 1
|
|
Dystonic Disorders
|
|
Ehlers-Danlos Syndrome Type 1
|
|
Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
|
|
Endometriosis
|
|
Esophageal Squamous Cell Carcinoma
|
|
Eye Abnormalities
|
|
Fatty Liver
|
|
Femoral Fractures
|
|
Fibrosis
|
|
Foot Deformities, Congenital
|
|
Heart Block
|
|
Heart-Hand Syndrome, Slovenian Type
|
|
Heart Valve Diseases
|
|
Hernia, Diaphragmatic
|
|
Hiv-Associated Lipodystrophy Syndrome
|
|
Cyclopia
|
|
Holoprosencephaly 3
|
|
Hyperinsulinism
|
|
Hyperlipidemias
|
|
Hyperostosis, Cortical, Congenital
|
|
Hypertension
|
|
Hypertriglyceridemia
|
|
Male Infertility
|
|
Insulin Resistance
|
|
Jaw Abnormalities
|
|
Keloid
|
|
Limb-Girdle Muscular Dystrophy, Type 1b
|
|
Lipodystrophy, Familial Partial
|
|
Liver Cirrhosis
|
|
Mammary Neoplasms, Animal
|
|
Mammary Neoplasms, Experimental
|
|
Mandibuloacral Dysplasia With Type A Lipodystrophy
|
|
Maxillary Neoplasms
|
|
Melanoma
|
|
Melanoma, Experimental
|
|
Meningioma
|
|
Microphthalmia, Isolated, With Coloboma 5
|
|
Microphthalmia, Syndromic 6
|
|
Muscular Dystrophy, Congenital, Lmna-Related
|
|
Nephrogenic Fibrosing Dermopathy
|
|
Nephrotic Syndrome
|
|
Neuroectodermal Tumors, Primitive
|
|
Obesity
|
|
Oral Submucous Fibrosis
|
|
Orofacial Cleft 11
|
|
Orofacial Cleft 5
|
|
Osteoarthritis
|
|
Osteogenesis Imperfecta
|
|
Osteogenesis Imperfecta, Type 2a
|
|
Osteogenesis Imperfecta, Type 3
|
|
Osteogenesis Imperfecta, Type 4
|
|
Osteoporosis
|
|
Osteosarcoma
|
|
Parkinson Disease, Secondary
|
|
Pierre Robin Syndrome
|
|
Polycystic Ovary Syndrome
|
|
Progeria
|
|
Prolactinoma
|
|
Pulmonary Fibrosis
|
|
Retinitis Pigmentosa 31
|
|
Scleroderma, Localized
|
|
Single Upper Central Incisor
|
|
Sinoatrial Block
|
|
Skeletal Defects, Genital Hypoplasia, And Mental Retardation
|
|
Skin Neoplasms
|
|
Tachycardia, Ventricular
|
|
Tight Skin Contracture Syndrome, Lethal
|
|
Tooth Abnormalities
|
|
Vitamin A Deficiency
|
|
Werner Syndrome
|
|
Witkop Syndrome
|
|
Abortion, Spontaneous
|
|
Wittwer Syndrome
|
|
Acth-Secreting Pituitary Adenoma
|
|
Lung Adenocarcinoma
|
|
Alzheimer's Disease
|
|
Ameloblastoma
|
|
Aneurysm, Dissecting
|
|
Anodontia
|
|
Anonychia Congenita
|
|
Aortic Valve Insufficiency
|
|
Psoriatic Arthritis
|
|
Rheumatoid Arthritis
|
|
Atrial Fibrillation
|
|
Autism Spectrum Disorder
|
|
Autoimmune Disease
|
|
Bone Resorption
|
|
Brain Neoplasms
|
|
Branchiootic Syndrome 3
|
|
Calcinosis
|
