scispace - formally typeset
J

Julia E. Parrish

Researcher at Baylor College of Medicine

Publications -  9
Citations -  1376

Julia E. Parrish is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Gene & Gene mapping. The author has an hindex of 8, co-authored 9 publications receiving 1302 citations. Previous affiliations of Julia E. Parrish include University of Texas Health Science Center at Houston & Human Genome Sequencing Center.

Papers
More filters
Journal ArticleDOI

The DNA sequence of the human X chromosome

Mark T. Ross, +282 more
- 17 Mar 2005 - 
TL;DR: This analysis illustrates the autosomal origin of the mammalian sex chromosomes, the stepwise process that led to the progressive loss of recombination between X and Y, and the extent of subsequent degradation of the Y chromosome.
Journal ArticleDOI

Selection Against Mutant Alleles in Blood Leukocytes is a Consistent Feature in Incontinentia Pigmenti Type 2

TL;DR: Fibroblast subclones from a biopsy at the boundary of a skin lesion in a newborn IP2 patient were isolated, and clones with either one or the other X active were identified, demonstrating that cells with the active disease-bearing X chromosome are still present in stage I skin lesions.
Journal ArticleDOI

A muscle-specific DNase I-like gene in human Xq28

TL;DR: A novel cDNA which maps to human Xq28 has been isolated and characterized and is predicted to contain a signal sequence at the amino terminus, a transmembrane domain near the carboxylterminus, and a helix-loop-helix domain.
Journal ArticleDOI

The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney

TL;DR: It is shown by fluorescence in situ hybridization and somatic cell hybrid analysis that the gene encoding human HCF, HCFC1, maps to the q28 region of the X chromosome.
Journal ArticleDOI

Methods for finding genes. A major rate-limiting step in positional cloning.

TL;DR: These techniques expand the size of the genomic region capable of being scanned for genes, while also allowing detection of genes regardless of their expression patterns.