Zobrazeno 1 - 10 of 61 pro vyhledávání: '"Diana M. Juriloff"'
1
Akademický článek
Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary Studies
Autor: Diana M. Juriloff, Muriel J. Harris
Publikováno v: Journal of Developmental Biology, Vol 6, Iss 3, p 22 (2018)
The human neural tube defects (NTD), anencephaly, spina bifida and craniorachischisis, originate from a failure of the embryonic neural tube to close. Human NTD are relatively common and both complex and heterogeneous in genetic origin, but the genet
Externí odkaz: https://doaj.org/article/58d8fcfe97ea42498894ca30f11eacad
Zobrazit plný text záznamu
3
Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain
Autor: Liane Gagnier, Muriel J. Harris, Diana M. Juriloff, Dixie L. Mager
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 100:772-788
Background: The heritable multifactorial etiology of human nonsyndromic cleft lip with or without cleft palate (CL ± P) is not understood. CL ± P occurs in 15% of neonates in the homozygous A/WySn mouse strain, with a multifactorial genetic etiolog
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3e57aa603335cbea4662ae386b9a7650
https://doi.org/10.1002/bdra.23320
Zobrazit plný text záznamu
5
Insights into the Etiology of Mammalian Neural Tube Closure Defects from Developmental, Genetic and Evolutionary Studies
Autor: Muriel J. Harris, Diana M. Juriloff
Publikováno v: Journal of Developmental Biology
Journal of Developmental Biology, Vol 6, Iss 3, p 22 (2018)
The human neural tube defects (NTD), anencephaly, spina bifida and craniorachischisis, originate from a failure of the embryonic neural tube to close. Human NTD are relatively common and both complex and heterogeneous in genetic origin, but the genet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c865f92e73bc431ea23f114cc621368a
https://doi.org/10.3390/jdb6030022
Zobrazit plný text záznamu
6
An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure
Autor: Diana M. Juriloff, Muriel J. Harris
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 88:653-669
The number of mouse mutants and strains with neural tube defects (NTDs) now exceeds 240, including 205 representing specific genes, 30 for unidentified genes, and 9 multifactorial strains. These mutants identify genes needed for embryonic neural tube
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::118cdb147174c696727c9244e2256a30
https://doi.org/10.1002/bdra.20676
Zobrazit plný text záznamu
7
Accelerated embryonic development associated with increased risk of neural tube defects induced by maternal diet in offspring of SELH/Bc mice
Autor: Muriel J. Harris, Diana M. Juriloff, Katharine L. Stoate
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 82:720-727
BACKGROUND: The SELH/Bc mouse strain has a high risk of the NTD, exencephaly, caused by multifactorial genetics. All SELH/Bc embryos have delayed elevation of neural folds; some never elevate (future exencephalics). Maternal diets affect SELH/Bc exen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd6fee06b2b6706245571d7f9abc9a75
https://doi.org/10.1002/bdra.20497
Zobrazit plný text záznamu
8
Mouse genetic models of cleft lip with or without cleft palate
Autor: Diana M. Juriloff, Muriel J. Harris
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 82:63-77
Nonsyndromic cleft lip and palate (CLP) is among the most common human birth defects. Transmission patterns suggest that the causes are "multifactorial" combinations of genetic and nongenetic factors, mostly distinct from those causing cleft secondar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d1d890d6f6312f105f8b60d804164ea
https://doi.org/10.1002/bdra.20430
Zobrazit plný text záznamu
9
Investigations of the genomic region that contains theclf1 mutation, a causal gene in multifactorial cleft lip and palate in mice
Autor: Diana M. Juriloff, Sarah L. Dewell, D. G. Mah, Carolyn J. Brown, Liane Gagnier, Muriel J. Harris, Dixie L. Mager
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 73:103-113
BACKGROUND Human nonsyndromic cleft lip and palate, CL(P), is genetically complex, with one contributing gene on chromosome 17q. A potentially homologous gene, clf1 on distal chromosome 11, is part of the digenic cause of the 10–30% CL(P) in the A/
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a504df8803fb6a66751f24c54e9d521b
https://doi.org/10.1002/bdra.20106
Zobrazit plný text záznamu
10
Maternal diet alters exencephaly frequency in SELH/Bc strain mouse embryos
Autor: Muriel J. Harris, Diana M. Juriloff
Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology. 73:532-540
BACKGROUND The SELH/Bc mouse inbred strain, with a high frequency of nonsyndromic, genetically-multifactorial exencephaly, is a model for human cranial neural tube defects (NTDs). Maternal diet affects risk of human NTDs. METHODS Exencephaly frequenc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d06ad5035715b2e3bd6303a9df440b5
https://doi.org/10.1002/bdra.20170
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje