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Dictionaries: Disease Related Concepts  Pathways  Sponge Compounds  Mode of action 

Human Genes+Proteins ( 0 1 2 3 4 5 6 7 8 9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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K

K10 -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   NEPPK [1]   WSN [1]   K13 [2]   K14 [2]   K16 [2]   K17 [2]   K2E [2]   K6A [2]  
BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FRAGILITY [1]   GENE THERAPY [1]   HAIR DISORDER [1]   IBS [1]   LESION [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PALMOPLANTAR KERATODERMA [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   STRESS [1]   TYPE I [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DISORDER [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   ICHTHYOSIS BULLOSA [2]   MONILETHRIX [2]   PACHYONYCHIA CONGENITA [2]   TRAUMA [2]   WHITE SPONGE NEVUS [2]  
CAUSE [1]   DISRUPT [1]   INACTIVATED [1]   LINKAGE [1]   ASSOCIATED [2]   MUTATION [2]   PRODUCE [2]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K12 -> 
  
HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K10 [1]   K13 [1]   K14 [1]   K16 [1]   K17 [1]   K18 [1]   K2E [1]   K6A [1]   K6B [1]  
BLISTER [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [1]   CRYPTOGENIC CIRRHOSIS [1]   DISORDER [1]   EPIDERMOLYSIS BULLOSA SIMPLEX [1]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   GENE THERAPY [1]   ICHTHYOSIS BULLOSA [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MONILETHRIX [1]   PACHYONYCHIA CONGENITA [1]   PREGNANCY [1]   TRAUMA [1]   TYPE I [1]   WHITE SPONGE NEVUS [1]  
ASSOCIATED [1]   DISRUPT [1]   INACTIVATED [1]   MUTATION [1]   PRODUCE [1]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K13 -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   KRT13 [1]   MIM [1]   NEPPK [1]   K10 [2]   K14 [2]   K16 [2]   K17 [2]   K2E [2]   K6A [2]   KERATIN 4 [2]   KERATIN 13 [4]   WSN [7]  
BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FAMILIAL [1]   GENE THERAPY [1]   HAIR DISORDER [1]   IBS [1]   IRREGULAR [1]   LEUKOKERATOSIS [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PALMOPLANTAR KERATODERMA [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   TYPE I [1]   ACANTHOSIS [2]   BENIGN [2]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DEFECT [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   FRAGILITY [2]   ICHTHYOSIS BULLOSA [2]   MONILETHRIX [2]   PACHYONYCHIA CONGENITA [2]   PARAKERATOSIS [2]   STRESS [2]   TRAUMA [2]   WHITE SPONGE NAEVUS [2]   HETEROZYGOUS [3]   LESION [3]   PLAQUE [4]   ORAL [6]   WHITE SPONGE NEVUS [6]   DISORDER [7]  
RENIERAMIDE [1]  
CAUSED [1]   DERIVATIVE [1]   DISRUPT [1]   INACTIVATED [1]   METABOLITE [1]   LINKAGE [2]   PRODUCE [2]   PRODUCT [2]   ASSOCIATED [3]   CAUSE [3]   AFFECT [4]   MUTATION [8]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K14 -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   NEPPK [1]   WSN [1]   K10 [2]   K13 [2]   K16 [2]   K17 [2]   K2E [2]   K6A [2]  
BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FRAGILITY [1]   GENE THERAPY [1]   HAIR DISORDER [1]   IBS [1]   LESION [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PALMOPLANTAR KERATODERMA [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   STRESS [1]   TYPE I [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DISORDER [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   ICHTHYOSIS BULLOSA [2]   MONILETHRIX [2]   PACHYONYCHIA CONGENITA [2]   TRAUMA [2]   WHITE SPONGE NEVUS [2]  
CAUSE [1]   DISRUPT [1]   INACTIVATED [1]   LINKAGE [1]   ASSOCIATED [2]   MUTATION [2]   PRODUCE [2]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K16 -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   NEPPK [1]   PPK [1]   WSN [1]   K10 [2]   K13 [2]   K14 [2]   K2E [2]   K6A [2]   K17 [3]  
ASSOCIATED DISEASE [1]   BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   DYSKERATOSIS CONGENITA [1]   ECTODERMAL DYSPLASIA [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FRAGILITY [1]   GENE THERAPY [1]   HAIR DISORDER [1]   HYPERKERATOSIS [1]   IBS [1]   KERATODERMA [1]   LEUKOKERATOSIS [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   STRESS [1]   TYPE I [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DISORDER [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   ICHTHYOSIS BULLOSA [2]   LESION [2]   MONILETHRIX [2]   PALMOPLANTAR KERATODERMA [2]   TRAUMA [2]   PACHYONYCHIA CONGENITA [3]   WHITE SPONGE NEVUS [3]  
CAUSE [1]   DISRUPT [1]   EXPRESSION [1]   INACTIVATED [1]   LINKAGE [1]   MUTATION [2]   PRODUCE [2]   ASSOCIATED [3]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K17 -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   NEPPK [1]   PPK [1]   WSN [1]   K10 [2]   K13 [2]   K14 [2]   K2E [2]   K6A [2]   K16 [3]  
ASSOCIATED DISEASE [1]   BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   DYSKERATOSIS CONGENITA [1]   ECTODERMAL DYSPLASIA [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FRAGILITY [1]   GENE THERAPY [1]   HAIR DISORDER [1]   HYPERKERATOSIS [1]   IBS [1]   KERATODERMA [1]   LEUKOKERATOSIS [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   STRESS [1]   TYPE I [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DISORDER [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   ICHTHYOSIS BULLOSA [2]   LESION [2]   MONILETHRIX [2]   PALMOPLANTAR KERATODERMA [2]   TRAUMA [2]   PACHYONYCHIA CONGENITA [3]   WHITE SPONGE NEVUS [3]  
CAUSE [1]   DISRUPT [1]   EXPRESSION [1]   INACTIVATED [1]   LINKAGE [1]   MUTATION [2]   PRODUCE [2]   ASSOCIATED [3]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K18 -> 
  
HHB6 [1]   K10 [1]   K12 [1]   K13 [1]   K14 [1]   K16 [1]   K17 [1]   K2E [1]   K6A [1]   K6B [1]   MDB [1]   TRANSGLUTAMINASE-2 [1]   INTERMEDIATE FILAMENT PROTEIN [2]  
ACUTE [1]   APOPTOSIS [1]   BLISTER [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [1]   CHRONIC HEPATITIS C [1]   CRYPTOGENIC CIRRHOSIS [1]   DEATH [1]   DISEASE PROGRESSION [1]   DISORDER [1]   DUCTAL [1]   EPIDERMOLYSIS BULLOSA SIMPLEX [1]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   FIBROSIS [1]   GENE THERAPY [1]   HETEROZYGOUS [1]   ICHTHYOSIS BULLOSA [1]   INFECTION [1]   INJURY [1]   LIVER DISEASE [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MONILETHRIX [1]   PACHYONYCHIA CONGENITA [1]   PREDISPOSITION [1]   PREGNANCY [1]   STRESS [1]   SUBACUTE [1]   TRAUMA [1]   TYPE I [1]   WHITE SPONGE NEVUS [1]  
PROTEOLYSIS [1]  
ASSOCIATED [1]   ASSOCIATION [1]   DISRUPT [1]   EXPRESSION [1]   INACTIVATED [1]   INCREASED [1]   PHOSPHORYLATION [1]   PRODUCE [1]   REGULATION [1]   MUTATION [2]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K19 -> 
  
HISTOLOGY [1]  
ATTACHMENT [1]   CONTROL [1]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K2E -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   NEPPK [1]   WSN [1]   K10 [2]   K13 [2]   K14 [2]   K16 [2]   K17 [2]   K6A [2]  
BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FRAGILITY [1]   GENE THERAPY [1]   HAIR DISORDER [1]   IBS [1]   LESION [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PALMOPLANTAR KERATODERMA [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   STRESS [1]   TYPE I [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DISORDER [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   ICHTHYOSIS BULLOSA [2]   MONILETHRIX [2]   PACHYONYCHIA CONGENITA [2]   TRAUMA [2]   WHITE SPONGE NEVUS [2]  
CAUSE [1]   DISRUPT [1]   INACTIVATED [1]   LINKAGE [1]   ASSOCIATED [2]   MUTATION [2]   PRODUCE [2]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]


K6A -> 
  
EPPK [1]   FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [1]   HHB6 [1]   INTERMEDIATE FILAMENT PROTEIN [1]   K12 [1]   K18 [1]   K6B [1]   NEPPK [1]   WSN [1]   K10 [2]   K13 [2]   K14 [2]   K16 [2]   K17 [2]   K2E [2]  
BCIE [1]   BLISTER [1]   CRYPTOGENIC CIRRHOSIS [1]   EPIDERMOLYSIS BULLOSA [1]   EPIDERMOLYTIC HYPERKERATOSIS [1]   FRAGILITY [1]   GENE THERAPY [1]   HAIR DISORDER [1]   IBS [1]   LESION [1]   MEESMANN'S CORNEAL DYSTROPHY [1]   MOSAICISM [1]   MUSCULAR DYSTROPHY [1]   PALMOPLANTAR KERATODERMA [1]   PREGNANCY [1]   STEATOCYSTOMA MULTIPLEX [1]   STRESS [1]   TYPE I [1]   BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA [2]   DISORDER [2]   EPIDERMOLYSIS BULLOSA SIMPLEX [2]   EPIDERMOLYTIC PALMOPLANTAR KERATODERMA [2]   ICHTHYOSIS BULLOSA [2]   MONILETHRIX [2]   PACHYONYCHIA CONGENITA [2]   TRAUMA [2]   WHITE SPONGE NEVUS [2]  
CAUSE [1]   DISRUPT [1]   INACTIVATED [1]   LINKAGE [1]   ASSOCIATED [2]   MUTATION [2]   PRODUCE [2]  

[draw networkshow hypotheses |   download as table: incl. pmid  excl. pmid]

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