Ian C. Welsh

Publication List Details

Period

2003 - 2009

Number

11

Co-Authors

Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass (2009)

Munroe, Robert J, Prabhu, Vinay, Acland, Greg M, Johnson, Kenneth R, Harris, Belinda S, O'Brien, Tim P, ...

Abstract Background The H6 homeobox genes Hmx1 , Hmx2 , and Hmx3 (also known as Nkx5-3 ; Nkx5-2 and Nkx5-1 , respectively), compose a family within the NKL subclass of the ANTP class of homeobox...

Evidence for a Conserved Function in Synapse Formation Reveals Phr1 as a Candidate Gene for Respiratory Failure in Newborn Mice (2003)

Robert W. Burgess, Kevin A. Peterson, Michael J. Johnson, Jeffrey J. Roix, Ian C. Welsh, Timothy P. O’brien

Genetic studies using a set of overlapping deletions centered at the piebald locus on distal mouse chromosome 14 have defined a genomic region associated with respiratory distress and lethality at...

Notch signaling regulates left–right asymmetry determination by inducing Nodal expression

Krebs, Luke T., Iwai, Naomi, Nonaka, Shigenori, Welsh, Ian C., Lan, Yu, Jiang, Rulang, ...

Generation of left–right asymmetry is an integral part of the establishment of the vertebrate body plan. Here we show that the Notch signaling pathway plays a primary role in the establishment of...

Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice

Frank, Aubrey C., Meyers, Kimberly A., Welsh, Ian C., O'Brien, Timothy P.

Mutagenesis screens to isolate a variety of alleles leading to null and non-null phenotypes represent an important approach for the characterization of gene function. Genetic schemes that use visible...

Evidence for a Conserved Function in Synapse Formation Reveals Phr1 as a Candidate Gene for Respiratory Failure in Newborn Mice

Burgess, Robert W., Peterson, Kevin A., Johnson, Michael J., Roix, Jeffrey J., Welsh, Ian C., O'Brien, Timothy P.

Genetic studies using a set of overlapping deletions centered at the piebald locus on distal mouse chromosome 14 have defined a genomic region associated with respiratory distress and lethality at...

Notch signaling regulates left–right asymmetry determination by inducing Nodal expression

Krebs, Luke T., Iwai, Naomi, Nonaka, Shigenori, Welsh, Ian C., Lan, Yu, Jiang, Rulang, ...

Generation of left–right asymmetry is an integral part of the establishment of the vertebrate body plan. Here we show that the Notch signaling pathway plays a primary role in the establishment of...

Development of an enhanced GFP-based dual-color reporter to facilitate genetic screens for the recovery of mutations in mice

Frank, Aubrey C., Meyers, Kimberly A., Welsh, Ian C., O'Brien, Timothy P.

Mutagenesis screens to isolate a variety of alleles leading to null and non-null phenotypes represent an important approach for the characterization of gene function. Genetic schemes that use visible...

Evidence for a Conserved Function in Synapse Formation Reveals Phr1 as a Candidate Gene for Respiratory Failure in Newborn Mice

Burgess, Robert W., Peterson, Kevin A., Johnson, Michael J., Roix, Jeffrey J., Welsh, Ian C., O'Brien, Timothy P.

Genetic studies using a set of overlapping deletions centered at the piebald locus on distal mouse chromosome 14 have defined a genomic region associated with respiratory distress and lethality at...