Normal fusion of developing eyelids requires coordination of inductive signals from the eyelid mesenchyme with migration of the periderm cell layer and constriction of the eyelids across the eye. Failure of this process results in an eyelids open at birth (EOB) phenotype in mice. We have identified a novel spontaneous allele of Alx4 that displays EOB, in addition to polydactyly and cranial malformations. Alx4 is expressed in the eyelid mesenchyme prior to and during eyelid fusion in a domain overlapping the expression of genes that also play a role in normal eyelid development. We show that Alx4 mutant mice have reduced expression of Fgf10, a key factor expressed in the mesenchyme that is required for initiation of eyelid fusion by the peri...
The sequential use of signaling pathways is essential for the guidance of pluripotent progenitors in...
Background Phenotype-driven screening of mouse mutations induced by ethylnitrosourea (ENU) leads t...
Mp is an irradiation-induced mouse mutation associated with microphthalmia, micropinna and hind limb...
Normal fusion of developing eyelids requires coordination of inductive signals from the eyelid mesen...
Aristaless-related genes are Paired-related homeobox genes that by definition encode a second strong...
There are conflicting reports about whether BMP signaling is required for eyelid closure during feta...
A group of mouse aristaless-related genes has been implicated in functions in the development of the...
Genetic control of craniofacial morphogenesis requires a complex interaction of numerous genes encod...
Gaping lids (gp) is an autosomal recessive mutation that arose spontaneously in the C57BL/6-ax stra...
AbstractEmbryonic eyelid closure involves forward movement and ultimate fusion of the upper and lowe...
Alx4 and Msx2 encode homeodomain-containing transcription factors that show a clear functional overl...
Genetic control of craniofacial morphogenesis requires a complex interaction of numerous genes encod...
BackgroundMicrophthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of e...
The vertebrate eye anlage grows out of the brain and folds into bilayered optic cups. The eye is pat...
PURPOSE. The purpose of the present study was to characterize a new slit-eye phenotype in the mouse....
The sequential use of signaling pathways is essential for the guidance of pluripotent progenitors in...
Background Phenotype-driven screening of mouse mutations induced by ethylnitrosourea (ENU) leads t...
Mp is an irradiation-induced mouse mutation associated with microphthalmia, micropinna and hind limb...
Normal fusion of developing eyelids requires coordination of inductive signals from the eyelid mesen...
Aristaless-related genes are Paired-related homeobox genes that by definition encode a second strong...
There are conflicting reports about whether BMP signaling is required for eyelid closure during feta...
A group of mouse aristaless-related genes has been implicated in functions in the development of the...
Genetic control of craniofacial morphogenesis requires a complex interaction of numerous genes encod...
Gaping lids (gp) is an autosomal recessive mutation that arose spontaneously in the C57BL/6-ax stra...
AbstractEmbryonic eyelid closure involves forward movement and ultimate fusion of the upper and lowe...
Alx4 and Msx2 encode homeodomain-containing transcription factors that show a clear functional overl...
Genetic control of craniofacial morphogenesis requires a complex interaction of numerous genes encod...
BackgroundMicrophthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of e...
The vertebrate eye anlage grows out of the brain and folds into bilayered optic cups. The eye is pat...
PURPOSE. The purpose of the present study was to characterize a new slit-eye phenotype in the mouse....
The sequential use of signaling pathways is essential for the guidance of pluripotent progenitors in...
Background Phenotype-driven screening of mouse mutations induced by ethylnitrosourea (ENU) leads t...
Mp is an irradiation-induced mouse mutation associated with microphthalmia, micropinna and hind limb...