K. S. Woods

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism (2005)

Woods, K.S., Cundall, M., Turton, J., Rizotti, K., Mehta, A., Palmer, R., ...

Duplications of Xq26-27 have been implicated in the etiology of X-linked hypopituitarism associated with mental retardation (MR). Additionally, an expansion of a polyalanine tract (by 11 alanines)...

Novel mutations within the POU1F1 gene associated with variable Combined Pituitary Hormone Deficiency (CPHD). (2005)

Turton, J.P., Reynaud, R., Mehta, A., Torpiano, J., Saveanu, A., Woods, K.S., ...

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD) (2005)

Turton, J. P., Mehta, A., Raza, J., Woods, K. S., Tiulpakov, A., Cassar, J., ...

The definitive version is available at www.blackwell-synergy.com

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD) (2005)

Turton, J. P., Mehta, A., Raza, J., Woods, K. S., Tiulpakov, A., Cassar, J., ...

The definitive version is available at www.blackwell-synergy.com

A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction (2003)

Carvalho, L.R., Woods, K.S., Mendonca, B.B., Marcal, N., Zamparini, A.L., Stifani, S., ...

The paired-like homeobox gene expressed in embryonic stem cells Hesx1/HESX1 encodes a developmental repressor and is expressed in early development in a region fated to form the forebrain, with...