Results: Lafora Disease

Results from Abstracts

Pick one of the followings

*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.

Legend:

***	p-value <= 0.001
**	p-value <= 0.01
*	p-value <= 0.05
n.s.	not significant

Top Ranked Genes, Molecules or Short Names*

Epm2a ***
Nhlrc1 **
Gbe1 *
Cln3 *
Mecp2 *
Bad n.s.
Dsp n.s.
C6 n.s.
C2 n.s.
C3 n.s.
Mal n.s.
Gaa n.s.
Cln5 n.s.
Uvrag n.s.
Lamp1 n.s.
Ppp1r3d n.s.
Scn1a n.s.
Bscl2 n.s.
Prdm8 n.s.
Serpini1 n.s.
Prep n.s.
Atg12 n.s.
Stbd1 n.s.
Pfkl n.s.
Sil1 n.s.
Dcp1a n.s.
Ca3 n.s.
Hipk2 n.s.
Hsf1 n.s.
Trim32 n.s.
Agl n.s.
Sgk1 n.s.
Tsen54 n.s.
Chrna4 n.s.
Scn1b n.s.
Nnat n.s.
Ppp1r3c n.s.
Ube2n n.s.
C3ar1 n.s.
Il10ra n.s.
Epm2aip1 n.s.
Map1lc3b n.s.
Ctcf n.s.
Ca2 n.s.
Ncl n.s.
Sv2a n.s.
Hspa5 n.s.
Gfap n.s.
Grasp n.s.
Kcnq2 n.s.
Kcnq3 n.s.
C4b n.s.
Erg n.s.
Cxcl10 n.s.
Il1b n.s.
Il6 n.s.
Ccl4 n.s.
Mtor n.s.
She n.s.
Mri n.s.
Myc n.s.
Mb n.s.
Camp n.s.
Ar n.s.
Cat n.s.
Set n.s.
Impact n.s.
Large n.s.

Top Ranked Mesh Terms

Male ***
Humans ***
Mutation ***
Pathology ***
Carrier proteins ***
Mice ***
Inclusion bodies ***
Metabolism ***
Lafora disease ***
Genetics ***
Glycogen ***
Brain ***
Female ***
Child ***
Protein tyrosine phosphatases non-receptor ***
Epilepsies myoclonic ***
Adolescent ***
Protein tyrosine phosphatases ***
Adult ***
Animals ***
Dual-specificity phosphatases ***
Electroencephalography ***
Glucans ***
Mice knockout ***
Diagnosis ***
Ubiquitin-protein ligases **
Skin **
Biopsy **
Autophagy **
Neurons **
Disease models animal **
Phosphorylation **
Molecular sequence data **
Protein binding **
Glycogen synthase **
Pedigree **
Chemistry **
Myoclonic epilepsies progressive **
Disease progression **
Microscopy electron **
Amino acid sequence **
Mice inbred c57bl **
Cerebral cortex **
Phenotype *
Proteasome endopeptidase complex *
Glucose *
Physiology *
Phosphates *
Mice transgenic *
Muscle skeletal *
Mutation missense *
Metabolism inborn errors *
Sleep rem *
Pakistan *
Photosensitivity disorders *
Ubiquitin *
Cos cells *
Haplotypes *
Young adult *
Age of onset *
Sirolimus *
Chickens *
Recombinant fusion proteins *
Atrophy *
Heterozygote *
Siblings *
Tubulin *
Liver *
Muscular diseases *
Leupeptins *
Unverricht-lundborg syndrome *
Phenylbutyrates *
Exons *
Molecular chaperones *
Proteostasis deficiencies *
Hsc70 heat-shock proteins *
Asphyxia *
Cystatin b *
Activities of daily living *
Chromosomes human pair 21 *
Aging *
Multiprotein complexes *
Cockayne syndrome *
Brain diseases *
Cerebellum *
Xeroderma pigmentosum *
Founder effect *
Microscopy fluorescence *
Middle aged *
Actins *
Arabidopsis proteins *
Hepatocytes *
Behavior animal *
Green fluorescent proteins *
Phagosomes *
Mammals *
Protein domains *
Eccrine glands *
Gaucher disease *
Glycogen debranching enzyme system *

Results for: Lafora Disease

Results from Abstracts

KEGG Pathways

Gene Ontology Biological Processes