User profiles for E. A. Lindsay
Elizabeth LindsayDepartment of Climate Change, Energy, the Environment and Water Verified email at dcceew.gov.au Cited by 632 |
Chromosomal microdeletions: dissecting del22q11 syndrome
EA Lindsay - Nature Reviews Genetics, 2001 - nature.com
Identifying the genes that underlie the pathogenesis of chromosome deletion and duplication
syndromes is a challenge because the affected chromosomal segment can contain many …
syndromes is a challenge because the affected chromosomal segment can contain many …
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
EA Lindsay, F Vitelli, H Su, M Morishima, T Huynh… - Nature, 2001 - nature.com
DiGeorge syndrome is characterized by cardiovascular, thymus and parathyroid defects and
craniofacial anomalies, and is usually caused by a heterozygous deletion of chromosomal …
craniofacial anomalies, and is usually caused by a heterozygous deletion of chromosomal …
Congenital heart disease in mice deficient for the DiGeorge syndrome region
EA Lindsay, A Botta, V Jurecic, S Carattini-Rivera… - Nature, 1999 - nature.com
The heterozygous chromosome deletion within the band 22q11 (del22q11) is an important
cause of congenital cardiovascular defects 1 . It is the genetic basis of DiGeorge syndrome …
cause of congenital cardiovascular defects 1 . It is the genetic basis of DiGeorge syndrome …
A systematic approach for using qualitative methods in primary prevention research
…, JR Gilbert, DMC Wilson, EA Lindsay… - Medical …, 1990 - Wiley Online Library
In this article we delineate a systematic approachfor incorporating qualitative methods in
research on primary prevention. Using examples from our studies of both smoking and …
research on primary prevention. Using examples from our studies of both smoking and …
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract
…, JN Wylie, RJ Schwartz, BG Bruneau, EA Lindsay… - 2004 - journals.biologists.com
Dysmorphogenesis of the cardiac outflow tract (OFT) causes many congenital heart defects,
including those associated with DiGeorge syndrome. Genetic manipulation in the mouse …
including those associated with DiGeorge syndrome. Genetic manipulation in the mouse …
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways
…, M Morishima, I Taddei, EA Lindsay… - Human molecular …, 2002 - academic.oup.com
TBX1 is the major candidate gene for DiGeorge syndrome (DGS). Mouse studies have shown
that the Tbx1 gene is haploinsufficient, as expected for a DGS candidate gene, and that it …
that the Tbx1 gene is haploinsufficient, as expected for a DGS candidate gene, and that it …
A genetic link between Tbx1 and fibroblast growth factor signaling
F Vitelli, I Taddei, M Morishima, EN Meyers, EA Lindsay… - 2002 - journals.biologists.com
Tbx1 haploinsufficiency causes aortic arch abnormalities in mice because of early growth
and remodeling defects of the fourth pharyngeal arch arteries. The function of Tbx1 in the …
and remodeling defects of the fourth pharyngeal arch arteries. The function of Tbx1 in the …
The abundance of microbial functional genes in grassy woodlands is influenced more by soil nutrient enrichment than by recent weed invasion or livestock exclusion
EA Lindsay, MJ Colloff, NL Gibb… - Applied and …, 2010 - Am Soc Microbiol
A diverse soil microbial community is involved in nitrogen cycling, and these microbes can
be affected by land management practices and weed invasion. We surveyed 20 woodlands …
be affected by land management practices and weed invasion. We surveyed 20 woodlands …
A randomized trial of a family physician intervention for smoking cessation
DM Wilson, DW Taylor, JR Gilbert, JA Best, EA Lindsay… - Jama, 1988 - jamanetwork.com
We assessed the impact of three conditions on one-year smoking cessation rates. Physicians
in 70 community general practices were randomly allocated by practice to one of three …
in 70 community general practices were randomly allocated by practice to one of three …
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments
…, LA Yuva-Paylor, A Baldini, EA Lindsay - Human molecular …, 2001 - academic.oup.com
Del22q11 syndrome is caused by heterozygous deletion of an ∼3 Mb segment of
chromosome 22q11.2. Children diagnosed with del22q11 syndrome commonly have learning …
chromosome 22q11.2. Children diagnosed with del22q11 syndrome commonly have learning …