Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Melissa LaBonty"'
Autor:
Chengtian Zhao, Viktoria Andreeva, Yann Gibert, Melissa LaBonty, Victoria Lattanzi, Shubhangi Prabhudesai, Yi Zhou, Leonard Zon, Kathleen L McCann, Susan Baserga, Pamela C Yelick
Publikováno v:
PLoS Genetics, Vol 10, Iss 1, p e1004074 (2014)
During vertebrate craniofacial development, neural crest cells (NCCs) contribute to most of the craniofacial pharyngeal skeleton. Defects in NCC specification, migration and differentiation resulting in malformations in the craniofacial complex are a
Externí odkaz:
https://doaj.org/article/ff5a4df20fab48319abd32252b34e238
Autor:
Melissa LaBonty, Cleo Szmygiel, Lauren E Byrnes, Samantha Hughes, Alison Woollard, Erin J Cram
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e101945 (2014)
Wnt signaling is tightly regulated during animal development and controls cell proliferation and differentiation. In C. elegans, activation of Wnt signaling alters the activity of the TCF/LEF transcription factor, POP-1, through activation of the Wnt
Externí odkaz:
https://doaj.org/article/05e4623340504059a5ef150e7d7232b4
Autor:
Courtney J. Haycraft, Mandy J. Croyle, Reagan S Andersen, Cameron LaFayette, Mikyla Scott, Bradley K. Yoder, Melissa R Bentley-Ford, Melissa LaBonty, Holly R. Thomas, John M. Parant
Publikováno v:
Genetics
Primary cilia are sensory and signaling hubs with a protein composition that is distinct from the rest of the cell due to the barrier function of the transition zone (TZ) at the base of the cilium. Protein transport across the TZ is mediated in part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03d5e05abaa017ea965f8dcbb7b86d06
https://europepmc.org/articles/PMC8733634/
https://europepmc.org/articles/PMC8733634/
Autor:
Melissa R Bentley-Ford, Holly R. Thomas, Mandy J. Croyle, Courtney J. Haycraft, Mikyla Scott, Bradley K. Yoder, Melissa LaBonty, Cameron LaFayette, John M. Parant
Primary cilia are sensory and signaling hubs with a protein composition that is distinct from the rest of the cell due to the barrier function of the transition zone (TZ) at the base of the cilium. Protein transport across the TZ is mediated in part
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23f24168881dd140b5bac9e2e76d71b3
https://doi.org/10.1101/2021.08.25.457729
https://doi.org/10.1101/2021.08.25.457729
Publikováno v:
Zebrafish. 15:536-545
Fibrodysplasia Ossificans Progressiva (FOP) is a rare, autosomal dominant genetic disorder in humans characterized by the gradual ossification of fibrous tissues, including skeletal muscle, tendons, and ligaments. In humans, mutations in the Type I B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e723e93cf63753029c09b4949af27fdd
https://doi.org/10.1089/zeb.2018.1611
https://doi.org/10.1089/zeb.2018.1611
Autor:
Melissa LaBonty, Pamela C. Yelick
Publikováno v:
Developmental Dynamics. 247:279-288
Fibrodysplasia Ossificans Progressiva is a rare human disease of heterotopic ossification. FOP patients experience progressive development of ectopic bone within fibrous tissues that contributes to a gradual loss of mobility and can lead to early mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f051ef4a8e38f3250c00c41ba51d06
https://doi.org/10.1002/dvdy.24606
https://doi.org/10.1002/dvdy.24606
Publikováno v:
Zebrafish. 15(6)
Fibrodysplasia Ossificans Progressiva (FOP) is a rare, autosomal dominant genetic disorder in humans characterized by the gradual ossification of fibrous tissues, including skeletal muscle, tendons, and ligaments. In humans, mutations in the Type I B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef5caa62ee8c7536cc90bb2c026616c7
https://pubmed.ncbi.nlm.nih.gov/30183553
https://pubmed.ncbi.nlm.nih.gov/30183553
Publikováno v:
Zebrafish. 14(4)
Fibrodysplasia ossificans progressiva (FOP) is a rare, autosomal dominant genetic disorder in humans characterized by explosive inflammatory response to injury leading to gradual ossification within fibrous tissues, including skeletal muscle, tendons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b2cfcc04fca4faf64f93a7cbbae2a8
https://pubmed.ncbi.nlm.nih.gov/28394244
https://pubmed.ncbi.nlm.nih.gov/28394244
Autor:
Pamela C. Yelick, Melissa LaBonty
Publikováno v:
The FASEB Journal. 29
Introduction: The zebrafish Type I TGFβ family member receptor, Alk8, modulates BMP/TGFβ signaling to promote cartilage and bone formation. Activating mutations in the human ortholog of Alk8, ACVR1...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67bc1ce8ad9fe14629052762bd0d66f3
https://doi.org/10.1096/fasebj.29.1_supplement.216.5
https://doi.org/10.1096/fasebj.29.1_supplement.216.5
Autor:
Lauren E. Byrnes, Cleo Szmygiel, Samantha Jane Hughes, Melissa LaBonty, Erin J. Cram, Alison Woollard
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 7, p e101945 (2014)
PLoS ONE, Vol 9, Iss 7, p e101945 (2014)
Wnt signaling is tightly regulated during animal development and controls cell proliferation and differentiation. In C. elegans, activation of Wnt signaling alters the activity of the TCF/LEF transcription factor, POP-1, through activation of the Wnt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ed12ce127865dd39c882d38e71f4339
https://pubmed.ncbi.nlm.nih.gov/24999833
https://pubmed.ncbi.nlm.nih.gov/24999833