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it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology

is a nuclear protein belonging to the nuclear hormone receptor family and NR2 subfamily with a nuclear receptor DNA-binding domain

which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes

The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer| composed of both platelet-derived growth factor receptor alpha and beta polypeptides

WT1 Polyclonal Antibody, 20ul Cell Separation and Collection Get your kit today andThis gene encodes a transcription factor that contains four zinc finger motifs at the C terminus and a proline glutamine rich DNA binding domain at the N terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and