Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Cairine Logan"'
Autor:
Lata Adnani, Rajiv Dixit, Xingyu Chen, Anjali Balakrishnan, Harshil Modi, Yacine Touahri, Cairine Logan, Carol Schuurmans
Publikováno v:
Biology Open, Vol 7, Iss 11 (2018)
The Plag gene family has three members; Plagl1/Zac1, which is a tumor suppressor gene, and Plag1 and Plagl2, which are proto-oncogenes. All three genes are known to be expressed in embryonic neural progenitors, and Zac1 regulates proliferation, neuro
Externí odkaz:
https://doaj.org/article/0ed1111a88fc433493063216a053ea02
Autor:
Nobuhiko Tachibana, Yacine Touahri, Rajiv Dixit, Luke Ajay David, Lata Adnani, Robert Cantrup, Tooka Aavani, Rachel O. Wong, Cairine Logan, Kyle C. Kurek, Carol Schuurmans
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 5 (2018)
PTEN hamartoma tumour syndrome (PHTS) is a heterogeneous group of rare, autosomal dominant disorders associated with PTEN germline mutations. PHTS patients routinely develop hamartomas, which are benign tissue overgrowths comprised of disorganized
Externí odkaz:
https://doaj.org/article/5e67aa0a2baf45eab61369be85e5394f
Autor:
Petra M. Hermann, C. Cairine Logan
Publikováno v:
BioTechniques, Vol 35, Iss 5, Pp 942-949 (2003)
Gene transfer by means of electroporation is an effective method for delivering DNA into cells. Expression vectors encoding green fluorescent protein (GFP) are routinely used as a control for this technique and are also regularly used to indirectly o
Externí odkaz:
https://doaj.org/article/6708ced73e95419594633fd0529d2544
Autor:
Anjali Balakrishnan, Xingyu Chen, Cairine Logan, Rajiv Dixit, Carol Schuurmans, Yacine Touahri, Lata Adnani, Harshil Modi
Publikováno v:
Biology Open, Vol 7, Iss 11 (2018)
Biology Open
Biology Open
The Plag gene family has three members; Plagl1/Zac1, which is a tumor suppressor gene, and Plag1 and Plagl2, which are proto-oncogenes. All three genes are known to be expressed in embryonic neural progenitors, and Zac1 regulates proliferation, neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f09c03b658c6aac9e89b950a6e5bd80
http://bio.biologists.org/content/7/11/bio038661
http://bio.biologists.org/content/7/11/bio038661
Autor:
Kyle C. Kurek, Robert Cantrup, Lata Adnani, Cairine Logan, Rajiv Dixit, Carol Schuurmans, Luke Ajay David, Yacine Touahri, Rachel O.L. Wong, Tooka Aavani, Nobuhiko Tachibana
Publikováno v:
Disease Models & Mechanisms.
PTEN hamartoma tumour syndrome (PHTS) is a heterogeneous group of rare, autosomal dominant disorders associated with PTEN germline mutations. PHTS patients routinely develop hamartomas, which are benign tissue overgrowths comprised of disorganized 'n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bda9fd6daadb86a49613d00f1b7e86f
https://doi.org/10.1242/dmm.031005
https://doi.org/10.1242/dmm.031005
Publikováno v:
Gene Expression Patterns. 14:42-54
The retina is comprised of one glial and six neuronal populations that are generated from a multipotent pool of retinal progenitor cells (RPCs) during development. To give rise to these different cell types, RPCs undergo temporal identity transitions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af26fb72422218f8561edb67050cd2c4
https://doi.org/10.1016/j.gep.2013.10.003
https://doi.org/10.1016/j.gep.2013.10.003
Publikováno v:
Molecular and Cellular Biology. 30:4339-4353
The Reelin-Disabled-1 (Dab1) signaling pathway plays a key role in the positioning of neurons during brain development. Two alternatively spliced Dab1 isoforms have been identified in chick retina and brain: Dab1-E, expressed at early stages of devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9b846b993f97a2422ee91ede6ebf563
https://doi.org/10.1128/mcb.00545-10
https://doi.org/10.1128/mcb.00545-10
Autor:
Suresh Nimmagadda, Winston Patrick Kuo, Marcela Buchtová, Cairine Logan, Eric Chiang, Joy M. Richman, Poongodi Geetha-Loganathan, Shari L. Benson, Timothy Au-Yeung, Katherine Fu
Publikováno v:
Developmental Dynamics. 239:574-591
The face is one of the three regions most frequently affected by congenital defects in humans. To understand the molecular mechanisms involved, it is necessary to have a more complete picture of gene expression in the embryo. Here, we use microarrays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a15198999c8d3e250e6b6245a4a0fa1c
https://doi.org/10.1002/dvdy.22135
https://doi.org/10.1002/dvdy.22135
Publikováno v:
Mammalian Genome. 16:815-824
We describe the isolation and molecular characterization of the chick ortholog of nyctalopin (NYX), the gene responsible for X-linked complete congenital stationary night blindness (CSNB1, also known as cCSNB). Chick Nyx (cNyx) comprises four exons s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d16bea2060f179c363319f4ceb8e1391
https://doi.org/10.1007/s00335-005-0018-y
https://doi.org/10.1007/s00335-005-0018-y
Autor:
Cairine Logan, Petra M. Hermann
Publikováno v:
BioTechniques. 35:942-949
Gene transfer by means of electroporation is an effective method for delivering DNA into cells. Expression vectors encoding green fluorescent protein (GFP) are routinely used as a control for this technique and are also regularly used to indirectly o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::278111ae162e3d882076252f3d5e2b67
https://doi.org/10.2144/03355st01
https://doi.org/10.2144/03355st01