Bristow, James

Mutant phenotypes for thousands of bacterial genes of unknown function

Price, M. N., Wetmore, K. M., Waters, R. J., Callaghan, M., Ray, J., Liu, H., Kuehl, J. V., Melnyk, R. A., Lamson, J. S., Suh, Y., et al. (2018) · Nature

Genomics and Phylogenetic StudiesBacterial Genetics and Biotechnology

Cited by 576

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency

Schalkwijk, J., Zweers, M. C., Steijlen, P. M., Dean, W. B., Taylor, G., van Vlijmen, I. M., van Haren, B., Miller, W. L., & Bristow, J. (2001) · New England Journal of Medicine

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 391

Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

Burch, G. H., Gong, Y., Liu, W., Dettman, R. W., Curry, C. J., Smith, L., Miller, W. L., & Bristow, J. (1997) · Nature Genetics

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 366

Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B

Bristow, J., Tee, M., Gitelman, S., Mellon, S., & Miller, W. (1993) · The Journal of cell biology

Cell Adhesion Molecules ResearchDevelopmental Biology and Gene Regulation

Cited by 302

Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition

Mao, J. R., Taylor, G., Dean, W. B., Wagner, D. R., Afzal, V., Lotz, J. C., Rubin, E. M., & Bristow, J. (2002) · Nature Genetics

Connective tissue disorders researchSkin and Cellular Biology Research

Cited by 261

The Ehlers-Danlos syndrome: on beyond collagens

Mao, J.-R., & Bristow, J. (2001) · Journal of Clinical Investigation

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 233

Loss of Bacterial Diversity during Antibiotic Treatment of Intubated Patients Colonized with Pseudomonas aeruginosa

Flanagan, J. L., Brodie, E. L., Weng, L., Lynch, S. V., Garcia, O., Brown, R., Hugenholtz, P., DeSantis, T. Z., Andersen, G. L., Wiener-Kronish, J. P., et al. (2007) · Journal of Clinical Microbiology

Nosocomial Infections in ICUBacterial biofilms and quorum sensing

Cited by 180

Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component/C4 gene locus

Morel, Y., Bristow, J., Gitelman, S. E., & Miller, W. L. (1989) · Proceedings of the National Academy of Sciences

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 158

Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus

Gitelman, S. E., Bristow, J., & Miller, W. L. (1992) · Molecular and Cellular Biology

Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities

Cited by 106

Embryonic expression of tenascin-X suggests a role in limb, muscle, and heart development

Burch, G. H., Bedolli, M. A., McDonough, S., Rosenthal, S. M., & Bristow, J. (1995) · Developmental Dynamics

Developmental Biology and Gene RegulationCongenital heart defects research

Cited by 105

Abundant adrenal-specific transcription of the human P450c21A “pseudogene.”

Bristow, J., Gitelman, S. E., Tee, M. K., Staels, B., & Miller, W. L. (1993) · Journal of Biological Chemistry

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 84

Tenascin‐X deficiency in autosomal recessive Ehlers–Danlos syndrome

Lindor, N. M., & Bristow, J. (2005) · American Journal of Medical Genetics Part A

Connective tissue disorders researchSkin and Cellular Biology Research

Cited by 67

Sequences promoting the transcription of the human XA gene overlapping P450c21A correctly predict the presence of a novel, adrenal-specific, truncated form of Tenascin-X

Tee, M. K., Thomson, A. A., Bristow, J., & Miller, W. L. (1995) · Genomics

Genomics and Chromatin DynamicsAdrenal Hormones and Disorders

Cited by 52