Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Haley A Nichols"'
Autor:
Chaitali Misra, Nita Sachan, Caryn Rothrock McNally, Sara N Koenig, Haley A Nichols, Anuradha Guggilam, Pamela A Lucchesi, William T Pu, Deepak Srivastava, Vidu Garg
Publikováno v:
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
Defects of atrial and ventricular septation are the most frequent form of congenital heart disease, accounting for almost 50% of all cases. We previously reported that a heterozygous G296S missense mutation of GATA4 caused atrial and ventricular sept
Externí odkaz:
https://doaj.org/article/8e619ecf80d14f26a44be5766806ce46
Autor:
Asha Acharya, Chetan P Hans, Sara N Koenig, Haley A Nichols, Cristi L Galindo, Harold R Garner, Walter H Merrill, Robert B Hinton, Vidu Garg
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27743 (2011)
Aortic valve calcification is the most common form of valvular heart disease, but the mechanisms of calcific aortic valve disease (CAVD) are unknown. NOTCH1 mutations are associated with aortic valve malformations and adult-onset calcification in fam
Externí odkaz:
https://doaj.org/article/60ee315398374ad38f0a0708a3f28785
Autor:
Brenna J. Christie, Erik L. Ireland, Rae A. Landers, Ross A. McCauley, Haley R. Nichols, Matthew T. Schendel
Publikováno v:
Western North American Naturalist. 72:296-310
The genus Quercus represents an important component of the scrublands and low forests of the Four Corners area of northeastern Arizona, southeastern Utah, southwestern Colorado, and northwestern New Mexico. The area is dominated by the widespread Que
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0f06de9cef69ee8fae57cae69a6c6dd
https://doi.org/10.3398/064.072.0304
https://doi.org/10.3398/064.072.0304
Autor:
Sara N. Koenig, William T. Pu, Vidu Garg, Chaitali Misra, Caryn Rothrock McNally, Pamela A. Lucchesi, Nita Sachan, Deepak Srivastava, Haley A. Nichols, Anuradha Guggilam
Publikováno v:
Misra, C; Sachan, N; McNally, CR; Koenig, SN; Nichols, HA; Guggilam, A; et al.(2012). Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo. PLoS Genetics, 8(5). doi: 10.1371/journal.pgen.1002690. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2hw8b3rx
PLoS genetics, vol 8, iss 5
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
PLoS Genetics
PLoS genetics, vol 8, iss 5
PLoS Genetics, Vol 8, Iss 5, p e1002690 (2012)
PLoS Genetics
Defects of atrial and ventricular septation are the most frequent form of congenital heart disease, accounting for almost 50% of all cases. We previously reported that a heterozygous G296S missense mutation of GATA4 caused atrial and ventricular sept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a55935dbfd1491aa2f545302fad73bb
http://www.escholarship.org/uc/item/2hw8b3rx
http://www.escholarship.org/uc/item/2hw8b3rx
Autor:
Chetan P Hans, Asha Acharya, Sara N Koenig, Haley A Nichols, Cristi L Galindo, Harold R Garner, Walter H Merrill, Robert B Hinton, Vidu Garg
Publikováno v:
Circulation Research. 109
Introduction: Aortic valve calcification is the most common form of valvular heart disease; however the mechanism(s) underlying calcific aortic valve disease (CAVD) are unknown. NOTCH1 mutations are associated with aortic valve malformations and adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b723bde6c394182ac2db00fee236f2e3
https://doi.org/10.1161/res.109.suppl_1.ap098
https://doi.org/10.1161/res.109.suppl_1.ap098
Autor:
Sara N. Koenig, Asha Acharya, Haley A. Nichols, Walter H. Merrill, Vidu Garg, Robert B. Hinton, Cristi L. Galindo, Harold R. Garner, Chetan P. Hans
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 11, p e27743 (2011)
PLoS ONE, Vol 6, Iss 11, p e27743 (2011)
Aortic valve calcification is the most common form of valvular heart disease, but the mechanisms of calcific aortic valve disease (CAVD) are unknown. NOTCH1 mutations are associated with aortic valve malformations and adult-onset calcification in fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043277ca9ef963ba27cd88ad540d442f
http://europepmc.org/articles/PMC3218038
http://europepmc.org/articles/PMC3218038
Autor:
Frederick F.B. Elder, Vidu Garg, Bill P Crider, Andrew R. Zinn, Haley A. Nichols, Lane Santos, Ashleigh A Richards, Natalie Hauser
Publikováno v:
Pediatric research. 64(4)
Congenital heart disease (CHD) is the most common type of birth defect, and the etiology of most cases is unknown. CHD often occurs in association with other birth malformations, and only in a minority are disease-causing chromosomal abnormalities id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12128125eefab5bb9d39d8c2edcd7c7a
https://pubmed.ncbi.nlm.nih.gov/18535492
https://pubmed.ncbi.nlm.nih.gov/18535492
Autor:
Haley A. Nichols, Meenakshi Maitra, Vidu Garg, Deepak Srivastava, Marie K. Schluterman, Cecilia W. Lo, James A. Richardson
Publikováno v:
Developmental Biology. (2):368-377
Congenital heart disease is the most common type of birth defect with an incidence of 1%. Previously, we described a point mutation in GATA4 that segregated with cardiac defects in a family with autosomal dominant disease. The mutation (G296S) exhibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::220e2a48209d67fe35646dc19b388a62