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
|