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Search Results for - MYASTHENIA GRAVIS

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
DNA
 
LCL
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
MYASTHENIA GRAVIS; MG
 
LCL
 
B-Lymphocyte
 
 
 
 
INCLUSION BODY MYOSITIS
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPERCHOLESTEROLEMIA, FAMILIAL; FHC
 
Fibroblast
 
Skin, Arm
 
 
 
 
HYPERCHOLESTEROLEMIA, FAMILIAL; FHC
 
DNA
 
Fibroblast
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
Fibroblast
 
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
Fibroblast
 
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
Fibroblast
 
 
 
 
 
EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES
 
Fibroblast
 
 
 
 
 
HYPERGLYCEROLEMIA | GLYCEROL KINASE; GK
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
Fibroblast
 
Skin, Arm
 
 
 
 
EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
Fibroblast
 
 
 
 
 
EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES
 
Fibroblast
 
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
DNA
 
LCL
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
LCL
 
B-Lymphocyte
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
Smooth muscle
 
Vein, iliac
 
 
 
 
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
Smooth muscle
 
Artery, iliac
 
 
 
 
APPARENTLY HEALTHY INDIVIDUAL
 
DNA
 
Smooth muscle
 
 
 
 
HYPERCHOLESTEROLEMIA, FAMILIAL; FHC | LOW DENSITY LIPOPROTEIN RECEPTOR; LDLR
 
DNA
 
Fibroblast
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
LCL
 
B-Lymphocyte
 
 
 
 
EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE; JEB3B | LAMININ, GAMMA-2; LAMC2
 
Fibroblast
 
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
DNA
 
LCL
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1 | COLLAGEN, TYPE V, ALPHA-1; COL5A1
 
LCL
 
B-Lymphocyte
 
 
 
 
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
 
LCL
 
B-Lymphocyte
 
 
 
 
PROPIONIC ACIDEMIA | PROPIONIC-COA CARBOXYLASE, BETA SUBUNIT; PCCB
 
DNA
 
LCL
 
 
 
 
PROPIONIC ACIDEMIA | PROPIONIC-COA CARBOXYLASE, BETA SUBUNIT; PCCB
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPERCHOLESTEROLEMIA, FAMILIAL; FHC | LOW DENSITY LIPOPROTEIN RECEPTOR; LDLR
 
Fibroblast
 
 
 
 
 
ANTI-CDKL5 (300-600 MOUSE)
 
Antibodies
 
 
 
 
 
IMMUNOGLOBULIN M, LEVEL OF
 
LCL
 
B-Lymphocyte
 
 
 
 
HTT-Q82-PCDNA3.1, PURE, 1-3144 (S13A)
 
Plasmid
 
 
 
 
 
HYPERCHOLESTEROLEMIA, FAMILIAL; FHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS
 
Somatic cell hybrid
 
 
 
 
 
HTT-Q82-PCDNA3.1, PURE, 1-586 (K444R)
 
Plasmid
 
 
 
 
 
HTT-Q81-PCDNA3.1, PURE, 1-586 (S13,16A)
 
Plasmid
 
 
 
 
 
ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS
 
DNA
 
Somatic cell hybrid
 
 
 
 
HTT-Q82-PCDNA3.1, PURE, 1-586 (S434A)
 
Plasmid
 

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