Yu-Ker Wang

发表

Frizzled 9 knock-out mice have abnormal B-cell development.

I. Weissman, U. Francke, E. Ranheim, 2005, Blood.

Frizzled 9 knockout mice have abnormal B cell development

U. Francke, E. Ranheim, T. Reya, 2004 .

frizzled 9 is expressed in neural precursor cells in the developing neural tube

U. Francke, M. Rao, M. Vetter, 2001, Development Genes and Evolution.

A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK.

U. Francke, R. Peoples, Y. Wang, 1998, Human molecular genetics.

Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion.

P. Kaplan, U. Francke, P. Kaplan, 1998, Genomics.

A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23.

R. Nusse, U. Francke, R. Peoples, 1997, Human molecular genetics.

The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion.

U. Francke, L. Pérez-Jurado, P. Kaplan, 1996, American journal of human genetics.

TBL2, a novel transducin family member in the WBS deletion: characterization of the complete sequence, genomic structure, transcriptional variants and the mouse ortholog

U. Francke, L. P. Pérez Jurado, J. Cruces, 1999, Cytogenetic and Genome Research.

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome.

K. Schughart, U. Francke, R. Spörle, 1999, Genomics.

The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome.

U. Francke, V. Godfrey, J. Derry, 1995, Genomics.