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FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays disease:Defects in NOTCH1 are a

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FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays disease:Defects in NOTCH1 are aFollicle stimulating hormone receptor encoded by FSHR belongs to family 1 of G protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants.

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Description

disease:Defects in NOTCH1 are a cause of aortic valve disease

This protein (annexin A1) inhibits phospholipase A2 and has anti-inflammatory activity

and that shares similarity with the intercellular adhesion molecule (ICAM) protein family

TGFB1/TGFB

Defects in this gene are the cause of LIG4 syndrome

FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays disease:Defects in NOTCH1 are aFollicle stimulating hormone receptor encoded by FSHR belongs to family 1 of G protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants.

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