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Nature Genetics|January 1, 1993
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndromeH L Hinds, C T Ashley, J S Sutcliffe, et al.The Journal of Pharmacology and Experimental Therapeutics|August 1, 1993
DOI and alpha-methylserotonin: comparative vascular and nonvascular smooth muscle effects and central 5-hydroxytryptamine2 receptor affinitiesM L Cohen, M P Johnson, K W Schenck, et al.Human Molecular Genetics|March 1, 1994
Frequency and stability of the fragile X premutationA L Reiss, H H Kazazian, C M Krebs, et al.Kidney International|October 1, 1989
In vivo T cell preactivation in chronic uremic hemodialyzed and non-hemodialyzed patientsG Beaurain, C Naret, L Marcon, et al.Nature Genetics|November 1, 1995
Evolution of the cryptic FMR1 CGG repeatE E Eichler, C B Kunst, K A Lugenbeel, et al.The Journal of Experimental Medicine|July 1, 1981
Characterization of a soluble suppressor of human B cell immunoglobulin biosynthesis produced by a continuous human suppressor T cell lineT A Fleisher, W C Greene, T Uchiyama, et al.Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|September 1, 1990
Studies of human leprosy lesions in situ using suction-induced blisters. 2. Cell changes and soluble interleukin 2 receptor (Tac peptide) in reversal reactionsD M Scollard, V Suriyanon, L Bhoopat, et al.The Journal of Clinical Investigation|August 1, 1980
Gluten-sensitive enteropathy. Influence of histocompatibility type on gluten sensitivity in vitroZ M Falchuk, D L Nelson, A J Katz, et al.Biochemistry|March 28, 1998
Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formationC E Pearson, E E Eichler, D Lorenzetti, et al.Pageof 55