Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Yu-Ker Wang is active.

Publication


Featured researches published by Yu-Ker Wang.


Development Genes and Evolution | 2001

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

Terence J. Van Raay; Yu-Ker Wang; Michael R. Stark; Jennifer T. Rasmussen; Uta Francke; Monica L. Vetter; Mahendra S. Rao

Abstract. The wnt signaling pathway has important functions in nervous system development. To better understand this process we have cloned and analyzed the expression of the wnt receptor, frizzled 9, in the developing nervous system in mouse, chick and zebrafish. The earliest expression of mouse frizzled 9 mRNA expression begins at E8.5 with expression throughout the entire rostral-caudal neuraxis. This early expression pattern within the neural tube appears to be conserved between chick and zebrafish. Expression becomes restricted to a ventral domain in the mouse ventricular zone at E11.5, a region specified to give rise to neurons and glia. Using a polyclonal antibody to MFZ9 further shows expression limited to neural restricted precursors cells.


Human Molecular Genetics | 1998

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

Luis A. Pérez Jurado; Yu-Ker Wang; Risa Peoples; Antonio Coloma; Jesús Cruces; Uta Francke


American Journal of Human Genetics | 2000

A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23.

Risa Peoples; Yvonne Franke; Yu-Ker Wang; Luis A. Pérez-Jurado; Tamar Paperna; Michael Cisco; Uta Francke


Human Molecular Genetics | 1997

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

Yu-Ker Wang; Cindy Harryman Samos; Risa Peoples; Luis A. Pérez-Jurado; Roel Nusse; Uta Francke


Blood | 2005

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

Erik A. Ranheim; Helen C Kwan; Tannishtha Reya; Yu-Ker Wang; Irving L. Weissman; Uta Francke


Genomics | 1999

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

Yu-Ker Wang; Ralf Spörle; Tamar Paperna; Klaus Schughart; Uta Francke


American Journal of Human Genetics | 1996

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

Risa Peoples; Luis A. Pérez-Jurado; Yu-Ker Wang; Uta Francke


Genomics | 1995

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

Jonathan M.J. Derry; Philipp Wiedemann; Patrick Blair; Yu-Ker Wang; Julie A. Kerns; Vanessa Lemahieu; Virginia L. Godfrey; Erby Wilkinson; Uta Francke


Genomics | 1998

A Mouse Single-Copy Gene, Gtf2i, the Homolog of Human GTF2I, That Is Duplicated in the Williams–Beuren Syndrome Deletion Region

Yu-Ker Wang; Luis A. Pérez-Jurado; Uta Francke


Genomics | 1998

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

Tamar Paperna; Risa Peoples; Yu-Ker Wang; Uta Francke

Collaboration


Dive into the Yu-Ker Wang's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Luis A. Pérez-Jurado

Instituto de Salud Carlos III

View shared research outputs
Top Co-Authors

Avatar

Erik A. Ranheim

University of Wisconsin-Madison

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge