The specification of C. elegans male tail ray six identity is governed by a group of genes involving mab-21. These genes are arranged in a linear genetic pathway. Vertebrate orthologues of these genes were each identified to be involved in eye development. As an initial step towards ascertaining whether the genetic relationships previously characterized in C. elegans are conserved in vertebrate eye development, I documented these transcripts’s temporal and spatial expression in zebrafish embryos. Furthermore, I perturbed the endogenous transcripts level through over-expression of mab21/2. In my study, I found that smad1 was up-regulated in mab21/2 over-expressed embryos. SMAD1 is the downstream effector of BMP4 in the BMP4 signaling pathway...
Resumen del póster presentado al 11th Meeting of the Spanish Society for Developmental Biology, cele...
Background: The genetic cascades underpinning vertebrate early eye morphogenesis are poorly understo...
Mutations in the MAB21L2 gene have been associated with major eye developmental malformations includ...
Mab21 homolog in Caenorhabditis elegans is expressed in the sensory ray, cells and determines the ra...
In Caenorhabditis elegans, the mab-21 gene plays an important role in cell fate specification. The m...
Mab21 gene family has its first member identified in C. elegans. Over the years, additional family m...
In the nematode worm C. elegans, ray patterning and the development of the male tail involve a compl...
The eye is an extremely delicate and complex structure that allows for all animalia to see the world...
The mab-21 gene was first identified in Caenorhabditis elegans as a critical component required for ...
Through in vivo loss-of-function studies, vertebrate members of the Male abnormal 21 (mab-21) gene f...
<p><b>A-K.</b> Expression pattern of <i>mab21l2</i> in zebrafish 18–72-hpf embryos. Whole mount imag...
We report the cloning and genetic characterization of one human and two murine homologs of the mab-2...
Abstract Background Through in vivo loss-of-function studies, vertebrate members of the Male abnorma...
Des mutations du gène MAB21l2 engendrent principalement des malformations développementales de l’œil...
The male tail of C. elegans is a complex structure composed of nine pairs of sensory rays embedded i...
Resumen del póster presentado al 11th Meeting of the Spanish Society for Developmental Biology, cele...
Background: The genetic cascades underpinning vertebrate early eye morphogenesis are poorly understo...
Mutations in the MAB21L2 gene have been associated with major eye developmental malformations includ...
Mab21 homolog in Caenorhabditis elegans is expressed in the sensory ray, cells and determines the ra...
In Caenorhabditis elegans, the mab-21 gene plays an important role in cell fate specification. The m...
Mab21 gene family has its first member identified in C. elegans. Over the years, additional family m...
In the nematode worm C. elegans, ray patterning and the development of the male tail involve a compl...
The eye is an extremely delicate and complex structure that allows for all animalia to see the world...
The mab-21 gene was first identified in Caenorhabditis elegans as a critical component required for ...
Through in vivo loss-of-function studies, vertebrate members of the Male abnormal 21 (mab-21) gene f...
<p><b>A-K.</b> Expression pattern of <i>mab21l2</i> in zebrafish 18–72-hpf embryos. Whole mount imag...
We report the cloning and genetic characterization of one human and two murine homologs of the mab-2...
Abstract Background Through in vivo loss-of-function studies, vertebrate members of the Male abnorma...
Des mutations du gène MAB21l2 engendrent principalement des malformations développementales de l’œil...
The male tail of C. elegans is a complex structure composed of nine pairs of sensory rays embedded i...
Resumen del póster presentado al 11th Meeting of the Spanish Society for Developmental Biology, cele...
Background: The genetic cascades underpinning vertebrate early eye morphogenesis are poorly understo...
Mutations in the MAB21L2 gene have been associated with major eye developmental malformations includ...