Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.

Por Giebel, L B, Spritz, R A
Publicado em 1991

RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR

Por Giebel, L.B., Spritz, R.A.
Publicado em 1990

Site-directed mutagenesis using a double-stranded DNA fragment as a PCR primer.

Por Giebel, L B, Spritz, R A
Publicado em 1990

Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.

Por Spritz, R A, Giebel, L B, Holmes, S A
Publicado em 1992

Nucleotide sequence of a processed human hsc70 pseudogene.

Por Giebel, L B, Dworniczak, B P, Bautz, E K
Publicado em 1987

A nonsense mutation in the tyrosinase gene of Afghan patients with tyrosinase negative (type IA) oculocutaneous albinism.

Por Giebel, L B, Musarella, M A, Spritz, R A
Publicado em 1991

A sequential dimerization mechanism for erythropoietin receptor activation.

Por Matthews, D J, Topping, R S, Cass, R T, Giebel, L B
Publicado em 1996

A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.

Por Giebel, L B, Tripathi, R K, King, R A, Spritz, R A
Publicado em 1991

Nucleotide sequence, evolution, and expression of the fetal globin gene of the spider monkey Ateles geoffroyi.

Por Giebel, L B, van Santen, V L, Slightom, J L, Spritz, R A
Publicado em 1985

A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.

Por Giebel, L B, Strunk, K M, King, R A, Hanifin, J M, Spritz, R A
Publicado em 1990

Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinism.

Por Giebel, L B, Tripathi, R K, Strunk, K M, Hanifin, J M, Jackson, C E, King, R A, Spritz, R A
Publicado em 1991