Results 41 to 50 of about 30,623 (153)
Requirement of Smurf-mediated endocytosis of Patched1 in sonic hedgehog signal reception
Cell surface reception of Sonic hedgehog (Shh) must ensure that the graded morphogenic signal is interpreted accordingly in neighboring cells to specify tissue patterns during development.
Shen Yue +10 more
doaj +1 more source
The relationship of Gata3 and Foxa2 targets with Shh+Ptch1−-/Shh−Ptch1+-pattern genes.
(A) The overlaps between Foxa2 targets in ChIP-seq with ABA ISH annotations and Shh+Ptch1−-/Shh−Ptch1+-pattern genes. (B) The overlaps between 84 Gata3 targets in ChIP-seq with ABA ISH annotations and Shh+Ptch1−-/Shh−Ptch1+-pattern genes.
Jinhua Liu (189844) +5 more
core +1 more source
Alterations in Morphology and Adult Neurogenesis in the Dentate Gyrus of Patched1 Heterozygous Mice
Many genes controlling neuronal development also regulate adult neurogenesis. We investigated in vivo the effect of Sonic hedgehog (Shh) signaling activation on patterning and neurogenesis of the hippocampus and behavior of Patched1 (Ptch1) heterozygous ...
Francesca Antonelli +12 more
doaj +1 more source
PTCH1 (patched homolog 1 (Drosophila))
Review on PTCH1 (patched homolog 1 (Drosophila)), with data on DNA, on the protein encoded, and where the gene is ...
Huret, JL, JL Huret
core +1 more source
Ptch2/Gas1 and Ptch1/Boc differentially regulate Hedgehog signalling in murine primordial germ cell migration. [PDF]
Gas1 and Boc/Cdon act as co-receptors in the vertebrate Hedgehog signalling pathway, but the nature of their interaction with the primary Ptch1/2 receptors remains unclear.
Cobourne, MT +9 more
core +1 more source
Unexpected phenotype in a frameshift mutation of PTCH1
Background Gorlin syndrome, also known as basal cell nevus syndrome (BCNS), is a rare autosomal dominant genetic condition, characterized by the presence of multiple basal cell carcinomas at a young age, odontogenic keratocysts, skeletal anomalies ...
Benedetta Beltrami +9 more
doaj +1 more source
Common genetic variations in Patched1 (PTCH1) gene and risk of hirschsprung disease in the Han Chinese population. [PDF]
Hirschsprung disease (HSCR) is the most frequent genetic cause of congenital intestinal obstruction with an incidence of 1:5000 live births. In a pathway-based epistasis analysis of data generated by genome-wide association study on HSCR, specific ...
Yang Wang +8 more
doaj +1 more source
PTCH1 (patched homolog 1 (Drosophila))
Review on PTCH1 (patched homolog 1 (Drosophila)), with data on DNA, on the protein encoded, and where the gene is ...
Lindstr
core +1 more source
Molecular alterations in basal cell carcinoma subtypes
A number of genes have been implicated in the pathogenesis of BCC in addition to the Hedgehog pathway, which is known to drive the initiation of this tumour. We performed in-depth analysis of 13 BCC-related genes (CSMD1, CSMD2, DPH3 promoter, PTCH1, SMO,
Lucia Di Nardo +15 more
doaj +1 more source
Indian Hedgehog (IHH) signaling, a key regulator of skeletal development, is highly activated in cartilage and bone tumors. Yet deletion of Ptch1, encoding an inhibitor of IHH receptor Smoothened (SMO), in chondrocyte or osteoblasts does not cause ...
Qi Deng +11 more
doaj +1 more source

