Braiterman, Lelita T.

Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy

Kemp, S., Wei, H.-M., Lu, J.-F., Braiterman, L. T., McGuinness, M. C., Moser, A. B., Watkins, P. A., & Smith, K. D. (1998) · Nature Medicine

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 249

X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes

Smith, K. D., Kemp, S., Braiterman, L. T., Lu, J.-F., Wei, H.-M., Geraghty, M., Stetten, G., Bergin, J. S., Pevsner, J., & Watkins, P. A. (1999) · Neurochemical Research

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 190

Scribble associates with two polarity proteins, Lgl2 and Vangl2, via distinct molecular domains

Kallay, L. M., McNickle, A., Brennwald, P. J., Hubbard, A. L., & Braiterman, L. T. (2006) · Journal of Cellular Biochemistry

Developmental Biology and Gene RegulationHippo pathway signaling and YAP/TAZ

Cited by 156

Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins

Braiterman, L. (1998) · Human Molecular Genetics

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 98

Expression of ALDP Is Altered in X‐linked Adrenoleukodystrophy

WATKINS, P. A., GOULD, S. J., SMITH, M. A., BRAITERMAN, L. T., WEI, H., KOK, F., MOSER, A. B., MOSER, H. W., & SMITH, K. D. (1996) · Annals of the New York Academy of Sciences

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 1