Regina Raz

The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome (2008)

Raz, Regina, Stricker, Sigmar, Elizabetta Gazzerro, Elizabetta, Clor, Julie L., Witte, Florian, Nistala, Harakiran, ...

Mutations in ROR2 result in a spectrum of genetic disorders in humans that are classified, depending on the nature of the mutation and the clinical phenotype, as either autosomal dominant...

Molecular Analysis of a Putative Transposable Retroelement from the Zea Genus with Internal Clusters of Tandem Repeats (1995)

Monfort, Amparo, Vicient, Carlos M., Raz, Regina, Puigdomènech, Pere, Martínez-Izquierdo, José A.

The molecular characterization of a recently discovered family of long repetitive sequences, termed ZLRS, is described. These elements belong to the class of moderate dispersed repetitive DNA and are...

Essential role of STAT3 for embryonic stem cell pluripotency

Raz, Regina, Lee, Chien-Kuo, Cannizzaro, Linda A., D’Eustachio, Peter, Levy, David E.

Propagation of mouse embryonic stem (ES) cells in vitro requires exogenous leukemia inhibitory factor (LIF) or related cytokines. Potential downstream effectors of the LIF signal in ES cells include...

Essential role of STAT3 for embryonic stem cell pluripotency

Raz, Regina, Lee, Chien-Kuo, Cannizzaro, Linda A., D’Eustachio, Peter, Levy, David E.

Propagation of mouse embryonic stem (ES) cells in vitro requires exogenous leukemia inhibitory factor (LIF) or related cytokines. Potential downstream effectors of the LIF signal in ES cells include...