DEVELOPMENT OF ANTISICKLING COMPOUNDS THAT CHEMICALLY MODIFY, HEMOGLOBIN S SPECIFICALLY WITHIN THE 2,3-DIPHOSPHOGLYCERATE BINDING SITEWALDER JA; WALDER RY; ARNONE A et al.1980; J. MOLEC. BIOL.; GBR; DA. 1980; VOL. 141; NO 2; PP. 195-216; BIBL. 2 P.Article

CLONING OF THE MSPI MODIFICATION ENZYME: THE SITE OF MODIFICATION AND ITS EFFECTS ON CLEAVAGE BY MSPI AND HPAIIWALDER RY; LANGTIMM CJ; RANJIT CHATTERJEE et al.1983; JOURNAL OF BIOLOGICAL CHEMISTRY; ISSN 0021-9258; USA; DA. 1983; VOL. 258; NO 2; PP. 1235-1241; BIBL. 51 REF.Article

MODIFICATION OF HEMOGLOBIN WITH ANALOGS OF ASPIRINZAUGG RH; WALDER JA; WALDER RY et al.1980; J. BIOL. CHEM.; USA; DA. 1980; VOL. 255; NO 7; PP. 2816-2821; BIBL. 19 REF.Article

CLONING AND EXPRESSION OF THE PST I RESTRICTION-MODIFICATION SYSTEM IN ESCHERICHIA COLIWALDER RY; HARTLEY JL; DONELSON JE et al.1981; PROC. NATL. ACAD. SCI. USA, BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 3; PP. 1503-1507; BIBL. 16 REF.Article

DIASPIRINS THAT CROSS-LINK BETA CHAINS OF HEMOGLOBIN: BIS(3,5-DIBROMOSALICYL) SUCCINATE AND BIS(3,5-DIBROMOSALICYL) FUMARATEWALDER JA; ZAUGG RH; WALDER RY et al.1979; BIOCHEMISTRY; USA; DA. 1979; VOL. 18; NO 20; PP. 4265-4270; BIBL. 16 REF.Article

MECHANISM FOR THE INCREASE IN SOLUBILITY OF DEOXYHEMOGLOBIN S DUE TO CROSS-LINKING THE BETA CHAINS BETWEEN LYSINE-82BETA ₁ AND LYSINE-82BETA ₂RANJIT CHATTERJEE; WALDER RY; ARNONE A et al.1982; BIOCHEMISTRY (EASTON); ISSN 0006-2960; USA; DA. 1982; VOL. 21; NO 23; PP. 5901-5909; BIBL. 1 P.Article

COMPLEMENTARY CARRIER PEPTIDE SYNTHESIS: GENERAL STRATEGY AND IMPLICATIONS FOR PREBIOTIC ORIGIN OF PEPTIDE SYNTHESISWALDER JA; WALDER RY; HELLER MJ et al.1979; PROC. NATION. ACAD. SCI. USA; USA; DA. 1979; VOL. 76; NO 1; PP. 51-55; BIBL. 14 REF.Article