User profiles for Laurie Smith

Laurie Smith

University of California San Diego
Verified email at ucsd.edu
Cited by 7304

[HTML][HTML] The RNA world of the nucleolus: two major families of small RNAs defined by different box elements with related functions

AG Balakin, L Smith, MJ Fournier - cell, 1996 - cell.com
We have discovered that all known yeast and vertebrate small nucleolar RNAs (snoRNAs),
except for the MRP/7–2 RNA, fall into two major classes. One class is defined by conserved …

A dominant mutation in the maize homeobox gene, Knotted-1, causes its ectopic expression in leaf cells with altered fates

LG Smith, BEN Greene, B Veit, S Hake - Development, 1992 - journals.biologists.com
Dominant mutations of the Knotted-1 (Kn1) homeobox gene of maize alter the differentiation
and growth of cells associated with leaf veins. By analyzing Kn1 transcripts and KN1 protein…

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

…, CJ Saunders, LK Willig, EG Farrow, LD Smith… - Science translational …, 2014 - science.org
Neurodevelopmental disorders (NDDs) affect more than 3% of children and are attributable
to single-gene mutations at more than 1000 loci. Traditional methods yield molecular …

Clonal analysis of hematopoietic stem-cell differentiation in vivo.

LG Smith, IL Weissman… - Proceedings of the …, 1991 - National Acad Sciences
Previous work has shown that the 0.02-0.05% of adult mouse bone marrow cells that bear
the cell surface phenotype Thy-1loLin-Sca-1+ are enriched 1000- to 2000-fold for …

Integration of omic networks in a developmental atlas of maize

…, RJ Schmitz, KJ Wu, MA Urich, JR Nery, LG Smith… - Science, 2016 - science.org
Coexpression networks and gene regulatory networks (GRNs) are emerging as important
tools for predicting functional roles of individual genes at a system-wide scale. To enable …

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

LK Willig, JE Petrikin, LD Smith… - The Lancet …, 2015 - thelancet.com
Background Genetic disorders and congenital anomalies are the leading causes of infant
mortality. Diagnosis of most genetic diseases in neonatal and paediatric intensive care units (…

Loss-of-function mutations in the maize homeobox gene, knotted1, are defective in shoot meristem maintenance

…, D Laudencia-Chingcuanco, LG Smith… - …, 1997 - journals.biologists.com
The product of the maize homeobox gene, knotted1 (kn1), localizes to the nuclei of cells in
shoot meristems, but is absent from portions of the meristem where leaf primordia or floral …

A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases

…, CJ Saunders, I Thiffault, SE Soden, LD Smith… - Genome medicine, 2015 - Springer
While the cost of whole genome sequencing (WGS) is approaching the realm of routine
medical tests, it remains too tardy to help guide the management of many acute medical …

Spatial control of cell expansion by the plant cytoskeleton

LG Smith, DG Oppenheimer - Annu. Rev. Cell Dev. Biol., 2005 - annualreviews.org
The cytoskeleton plays important roles in plant cell shape determination by influencing the
patterns in which cell wall materials are deposited. Cortical microtubules are thought to orient …

Glycosaminoglycans can modulate extracellular localization of the wingless protein and promote signal transduction.

F Reichsman, L Smith, S Cumberledge - The Journal of cell biology, 1996 - rupress.org
Wingless, the Drosophila homologue of the proto-oncogene Wnt-1, encodes a secreted
glycoprotein that regulates differentiation and proliferation of nearby cells. Here we report on the …