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Human Molecular Genetics|December 1, 1995
Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptionsE E Eichler, H A Hammond, J N Macpherson, et al.
The Journal of Biological Chemistry|March 15, 1989
Purification and characterization of a calcium-dependent ATPase from Paramecium tetraureliaA E Levin, S M Travis, L D DeVito, et al.
Annals of Internal Medicine|October 1, 1986
The human interleukin-2 receptor: normal and abnormal expression in T cells and in leukemias induced by the human T-lymphotropic retrovirusesW C Greene, W J Leonard, J M Depper, et al.
Life Sciences|January 1, 1990
The cloning and sequence analysis of the rat serotonin-1A receptor geneY Fujiwara, D L Nelson, K Kashihara, et al.
The Plant Cell|February 4, 2023
Linking discoveries, mechanisms, and technologies to develop a clearer perspective on plant long noncoding RNAsKyle Palos, Li'ang Yu, Caylyn E Railey, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakageS T Warren, S J Knight, J F Peters, et al.
Cancer Research|December 5, 2000
TMS1, a novel proapoptotic caspase recruitment domain protein, is a target of methylation-induced gene silencing in human breast cancersK E Conway, B B McConnell, C E Bowring, et al.
American Journal of Medical Genetics|August 9, 1996
A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 geneA M Lachiewicz, G A Spiridigliozzi, A McConkie-Rosell, et al.
Blood|December 10, 1999
Regulation and function of WASp in platelets by the collagen receptor, glycoprotein VIB S Gross, J I Wilde, L Quek, et al.
American Journal of Medical Genetics|July 15, 1994
Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testingG S Fisch, D L Nelson, K Snow, et al.
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