Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Rebecca S. Reiter"'
Autor:
Todd E. Scheetz, Chad A. Roberts, Tamara A. Kucaba, Jim J.-C. Lin, Thomas L. Casavant, Shereen Chang, Rebecca S. Reiter, M. Bento Soares, Jennifer J.S. Laffin, Mari E. Eyestone, Hakeem Abdulkawy, Dylan Tack, Bartley Brown, Maria de Fatima Bonaldo, Val C. Sheffield
Publikováno v:
Physiological Genomics. 17:245-252
Congenital heart defects affect ∼1,000,000 people in the United States, with 40,000 new births contributing to that number every year. A large percentage of these defects can be attributed to septal defects. We assembled a nonredundant collection o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc36368b0ca9173950e86c19e2befcc
https://doi.org/10.1152/physiolgenomics.00186.2003
https://doi.org/10.1152/physiolgenomics.00186.2003
Publikováno v:
Developmental Dynamics. 225:233-240
The specific roles of vascular endothelial growth factor (VEGF) family members and their receptors (VEGFRs) in coronary vessel formation were studied. By using the quail heart explant model, we found that neutralizing antibodies to VEGF-B or VEGF-C i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1905ec2b10b77e4fef119f779952c44
https://doi.org/10.1002/dvdy.10158
https://doi.org/10.1002/dvdy.10158
Publikováno v:
The Anatomical Record. 263:72-84
In vertebrates, three troponin T (TnT) genes, cardiac TnT (cTnT), skeletal muscle fast-twitch TnT (fTnT), and slow-twitch TnT (sTnT), have evolved for the regulation of striated muscle contraction. To understand the mechanism for muscle fiber-specifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6440e880e46aee8b8617995ae9268351
https://doi.org/10.1002/ar.1078
https://doi.org/10.1002/ar.1078
Autor:
Charles S. Searby, Wallace L.M. Alward, Ruth E. Swiderski, Val C. Sheffield, Edwin M. Stone, Darryl Y. Nishimura, Rebecca S. Reiter, Jeffrey W. Kalenak, Jim J.-C. Lin
Publikováno v:
Developmental Dynamics. 216:16-27
The transcription factor FKHL7 gene has recently been associated with the ante- rior segment dysgenesis disorder of the eye known as Axenfeld-Rieger anomaly (ARA). A grow- ing body of evidence indicates that mutations in FKHL7 cause not only defects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba3a3003b4a148e35ff125844327bde
https://doi.org/10.1002/(sici)1097-0177(199909)216:1<16::aid-dvdy4>3.0.co
https://doi.org/10.1002/(sici)1097-0177(199909)216:1<16::aid-dvdy4>3.0.co
Autor:
Qin Wang, Thomas M. Schultheiss, Sylvia Evans, Da-Zhi Wang, Jenny Li-Chun Lin, Sonja L. Krob, Haley S. Williams, Jim J.-C. Lin, Rebecca S. Reiter
Publikováno v:
Development. 126:1281-1294
A novel gene, Xin, from chick (cXin) and mouse (mXin) embryonic hearts, may be required for cardiac morphogenesis and looping. Both cloned cDNAs have a single open reading frame, encoding proteins with 2,562 and 1,677 amino acids for cXin and mXin, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66a4e51cc212c51ef2ae077b8c35e2b5
https://doi.org/10.1242/dev.126.6.1281
https://doi.org/10.1242/dev.126.6.1281
Autor:
Elena V. Semina, Jeffrey C. Murray, Sandra Daack-Hirsch, Rebecca S. Reiter, Helen A. Mintz-Hittner, Carrie D. Funkhauser, Robert E. Ferrell, Pierre Bitoun, Wallace L.M. Alward
Publikováno v:
Nature Genetics. 19:167-170
We report here the identification of a new human homeobox gene, PITX3, and its involvement in anterior segment mesenchymal dysgenesis (ASMD) and congenital cataracts in humans. The PITX3 gene is the human homologue of the mouse Pitx3 gene and is a me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15361f7ca8099ce012764d2c4f5c3d74
https://doi.org/10.1038/527
https://doi.org/10.1038/527
Publikováno v:
Genomics. 50:61-68
Homeobox-containing genes play an important role in development, including positional specification of the body plan and organogenesis. We previously isolated the human HMX1 (H6) gene, a novel homeobox-containing gene of the HMX family, from a human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78fbcceef87c4dea0ed7b9ebc355dcdd
https://doi.org/10.1006/geno.1998.5284
https://doi.org/10.1006/geno.1998.5284
Autor:
J A Maynard, Kenneth J. Noonan, James A. Martin, Gail L. Kurriger, Jeff W. Stevens, Rebecca S. Reiter
Publikováno v:
Journal of Orthopaedic Research. 16:100-103
Hyaluronan is an integral component of proteoglycan-rich extracellular matrices such as hyaline cartilage. Hyaluronan is commonly found in embryonic tissue and is important in the formation of hydrated matrices that allow cellular expansion and migra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa1d9096d5d3b018a8935a7c68df92c
https://doi.org/10.1002/jor.1100160117
https://doi.org/10.1002/jor.1100160117
Publikováno v:
Human Molecular Genetics. 6:2109-2116
We recently reported the positional cloning of a homeobox gene involved in the pathogenesis of Rieger syndrome, RIEG1 , and its mouse homolog, Rieg1 . Rieg1 (also independently described as Pitx2) is highly homologous to the Ptx1/Potx gene product, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51ed1e51e2070f54d33dedbbf9c336b6
https://doi.org/10.1093/hmg/6.12.2109
https://doi.org/10.1093/hmg/6.12.2109
Autor:
Marina D'Alessio, Michael Solursh, Rebecca S. Reiter, Maurizio Di Liberto, Jean-Yves Exposito, Hiroaki R. Suzuki, Francesco Ramirez, Roberto Gambino
Publikováno v:
Zoological Science. 14:449-454
The time of appearance and location of three distinct collagen gene transcripts termed 1 alpha, 2 alpha, and 3 alpha, were monitored in the developing S. purpuratus embryo by in situ hybridization. The 1 alpha and 2 alpha transcripts of fibrillar col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3b782c751ec08544dc1ce7e882c406b
https://doi.org/10.2108/zsj.14.449
https://doi.org/10.2108/zsj.14.449