NE	Nuclear envelope
LINC	Linker of nucleoskeleton and cytoskeleton
EDMD	Emery–Dreifuss muscular dystrophy
ADLD	Autosomal dominant leukodystrophy
CMT	Charcot–Marie–Tooth
HGPS	Hutchinson–Gilford progeria syndrome
APLD	Acquired partial lipodystrophy (Barraquer–Simons syndrome)
LGMD	Limb–girdle muscular dystrophy
PHA	Pelger–Hue’t anomaly
HEM/GRBGD	Greenberg hydrops-ectopic calcification-moth-eaten skeletal dysplasia
BOS	Buschke–Ollendorff syndrome
ECM	Extracellular matrix
INM	Inner nuclear membrane
NL	Nuclear lamina
IF	Intermediate filaments
NLS	Nuclear localization signal/sequence
NPC	Nuclear pore complex
Cdk	Cyclin-Dependent Kinase
PKA	Protein Kinase A
PKC	Protein Kinase C
Gsk	Glycogen Synthase Kinase
ERK	Extracellular Signal-Regulated Kinase
MAPK/APK	Mitogen-Activated Protein Kinase/Activated Protein Kinase
S/MAR	Scaffold/matrix attachment region
cAMP	Cyclic Adenosine Monophosphate
GFP	Green Fluorescent Protein
CNS	Central Nervous System
IMD	Immune deficiency
Top2	Topoisomerase II
SRPK	Serine/Arginine Protein Kinase
LEM	LAP2-Emerin-MAN1 Domain Protein
MEF	Myocyte Enhancer Factor 2
MYF	Myogenic Factor
DMD	Duchenne Muscular Dystrophy
TOR	Target of Rapamycin
Nrf	Nuclear Factor Erythroid
NOX	NADPH Oxidase
IFM	Indirect flight muscle
AMPK	Activated protein kinase
FOXO	Forkhead box O
NPS	Neuropeptide S
HSF	Heat Shock Factor
CMD	Congenital muscular dystrophy
TM	Transmembrane
TMEM	Transmembrane Protein
BAF	Barrier-to-Autointegration Factor
LAP	Lamina-associated polypeptide
MAN	Inner Nuclear Membrane Protein
LEMD1	LEM Domain-Containing 1
EMD	Emerin
ANKL	Ankyrin Repeat and LEM Domain-Containing
BOKS	Barrier-to-Autointegration Factor (BAF)-binding protein of KASH domain
OTE	Otefin
NES	Nuclear Export Signal
MSC	MAN1/Src1p/C-terminal motif
ANK	Ankyrin repeats
RM	RNA Recognition Motif
GIY-YIG	Endonuclease Domain (a conserved DNA-binding motif)
LBR	Lamin B Receptor
HEM	Hydrops-Ectopic calcification-Moth-eaten skeletal dysplasia
LBS	Lamin binding site
CHD	Chromodomain-Helicase-DNA-binding protein
ABS	Acting binding side
AMC	Arthrogryposis multiplex congenital
MCPHRb	MicrocephalyRetinoblastoma
GSSG	Glutathione Disulfide
GSH	Reduced glutathione
wt	Wild type