List of works - Sally H Cross

A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected].

scientific article

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

scientific article published on 6 July 2006

Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development

scientific article

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy

scientific article

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

scientific article published on 16 January 2020

Genomic anatomy of the Tyrp1 (brown) deletion complex

scholarly article

Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes

scientific article

Genotype-phenotype correlation of mouse pde6b mutations

scientific article published in September 2005

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.

scientific article published on 18 May 2004

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse: Supplemental Information

article

Mouse mutations cause retinal degeneration and reduced mitochondrial function

scientific article published on 18 December 2018

Novel ENU-induced eye mutations in the mouse: models for human eye disease

scientific article

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

scientific article

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype

scientific article

The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells.

scientific article published on 5 November 2015

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification

scientific article published on 01 April 2020

Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor

scientific article published in July 2004

List of works by Sally H Cross

A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected].

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

Genomic anatomy of the Tyrp1 (brown) deletion complex

Genomic structure and chromosomal mapping of the murine and human Mbd1, Mbd2, Mbd3, and Mbd4 genes

Genotype-phenotype correlation of mouse pde6b mutations

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse: Supplemental Information

Mouse mutations cause retinal degeneration and reduced mitochondrial function

Novel ENU-induced eye mutations in the mouse: models for human eye disease

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype

The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells.

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification

Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor