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index medicus (196) 196
humans (152) 152
animals (123) 123
cell biology (104) 104
proteins (71) 71
mutation (61) 61
lamin type b - genetics (56) 56
biochemistry & molecular biology (49) 49
mice (49) 49
a-type lamins (45) 45
dreifuss muscular-dystrophy (45) 45
gene expression (40) 40
lamins (40) 40
lamin type b - metabolism (39) 39
integumentary system (37) 37
lamin b1 (37) 37
nuclear envelope (37) 37
congenital, hereditary, and neonatal diseases and abnormalities (36) 36
lamin type a - genetics (36) 36
female (35) 35
nuclear lamina (34) 34
expression (33) 33
hutchinson-gilford-progeria (33) 33
chromatin (32) 32
embryonic structures (32) 32
genetic aspects (32) 32
genetics & heredity (32) 32
intermediate filament proteins (32) 32
lamin (32) 32
nuclear envelope - metabolism (32) 32
research (32) 32
male (31) 31
article (29) 29
biology (29) 29
cell nucleus - metabolism (29) 29
genes (29) 29
laminopathies (28) 28
molecular sequence data (27) 27
nuclear proteins - metabolism (27) 27
organization (27) 27
analysis (26) 26
lamin type a - metabolism (26) 26
lamins - genetics (26) 26
disease (25) 25
nuclear lamina - metabolism (25) 25
amino acid sequence (24) 24
lamins - metabolism (24) 24
middle aged (24) 24
neurosciences (24) 24
nuclear-envelope (23) 23
phenotype (23) 23
animal structures (22) 22
research article (22) 22
cells (21) 21
b-type lamins (20) 20
aging (19) 19
cancer (19) 19
clinical neurology (19) 19
dilated cardiomyopathy (19) 19
familial partial lipodystrophy (19) 19
genomics (19) 19
nuclear proteins - genetics (19) 19
physiological aspects (19) 19
progeria (19) 19
adult (18) 18
gene (18) 18
autosomal-dominant leukodystrophy (17) 17
cells, cultured (17) 17
gene mutations (17) 17
mutation - genetics (17) 17
partial lipodystrophy (17) 17
progressive multiple-sclerosis (17) 17
cell line (16) 16
fibroblasts - metabolism (16) 16
life sciences (16) 16
medicine (16) 16
molecular biology (16) 16
prelamin-a (16) 16
protein binding (16) 16
cell cycle (15) 15
emerin (15) 15
health aspects (15) 15
lamin a (15) 15
multidisciplinary sciences (15) 15
muscular dystrophy (15) 15
neurology (15) 15
senescence (15) 15
autonomic symptoms (14) 14
chromatin - metabolism (14) 14
cytoskeleton (14) 14
developmental biology (14) 14
gene-expression (14) 14
mutations (14) 14
protein (14) 14
signal transduction (14) 14
cause autosomal-dominant (13) 13
cellular biology (13) 13
differentiation (13) 13
drosophila (13) 13
envelope (13) 13
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Journal Article
Journal Article
Irish medical journal, ISSN 0332-3102, 06/2012, Volume 105, Issue 6, pp. 186 - 187
The hereditary leukodystrophies are rare disorders caused by molecular abnormalities leading to destruction of or failure of development of central white... 
Magnetic Resonance Imaging | Lamin Type B - genetics | Humans | Middle Aged | Age of Onset | Male | Disease Progression | Hereditary Central Nervous System Demyelinating Diseases - epidemiology | Hereditary Central Nervous System Demyelinating Diseases - genetics
Journal Article
Human Mutation, ISSN 1059-7794, 08/2013, Volume 34, Issue 8, pp. 1160 - 1171
Journal Article
Journal Article
Journal Article
NEURORADIOLOGY, ISSN 0028-3940, 08/2013, Volume 55, Issue 8, pp. 933 - 939
Journal Article
neurogenetics, ISSN 1364-6745, 2/2011, Volume 12, Issue 1, pp. 65 - 72
Journal Article
Journal Article
Journal Article
Journal Article
European Journal of Neurology, ISSN 1351-5101, 04/2010, Volume 17, Issue 4, pp. 541 - 549
Journal Article