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DOMINANT AND RECESSIVE INFORMATIONAL SUPPRESSORS OF A MISSENSE MUTATION IN COPRINUS.SEALY LEWIS HM; CASSELTON LA.1977; MOLEC. GEN. GENET.; GERM.; DA. 1977; VOL. 151; NO 2; PP. 189-195; BIBL. 21 REF.Article

EVIDENCE THAT BACTERIOPHAGE T4 EPH1 IS A MISSENSE HOC MUTATIONCHILDS JD; PILON R.1983; JOURNAL OF VIROLOGY; ISSN 0022-538X; USA; DA. 1983; VOL. 46; NO 2; PP. 629-631; BIBL. 5 REF.Article

DEGRADATION OF MISSENSE MUTANT BETA -GALACTOSIDASE PROTEINS IN ESCHERICHIA COLI K-12.BERGQUIST PL; TRUMAN P.1978; MOLEC. GEN. GENET.; DEU; DA. 1978; VOL. 164; NO 1; PP. 105-108; BIBL. 17 REF.Article

A novel missense mutation (Leu46Val) of PAX6 found in an autistic patientMAEKAWA, Motoko; IWAYAMA, Yoshimi; MAEKAWA, Nobuo et al.Neuroscience letters. 2009, Vol 462, Num 3, pp 267-271, issn 0304-3940, 5 p.Article

MISSENSE MUTATIONS IN THE LACZ GENE THAT RESULT IN DEGRADATION OF BETA -GALACTOSIDASE STRUCTURAL PROTEIN.ZIPSER D; PRABHAKAR BHAVSAR.1976; J. BACTERIOL.; U.S.A.; DA. 1976; VOL. 127; NO 3; PP. 1538-1542; BIBL. 14 REF.Article

Thanatophoric Dysplasia Caused by Double Missense FGFR3 MutationsPANNIER, Stéphanie; MARTINOVIC, Jelena; HEUERTZ, Solange et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 6, pp 1296-1301, issn 1552-4825, 6 p.Article

IN VIVO AND IN VITRO FUNCTIONAL ALTERATIONS OF THE BACTERIOPHAGE LAMBDA RECEPTOR IN LAMB MISSENSE MUTANTS OF ESCHERICHIA COLI K-12BRAUN BRETON C; HOFNUNG M.1981; J. BACTERIOL.; ISSN 0021-9193; USA; DA. 1981; VOL. 148; NO 3; PP. 845-852; BIBL. 20 REF.Article

PRIMARY SITE AND SECOND SITE REVERTANTS OF MISSENSE MUTANTS OF THE EVOLUTIONARILY INVARIANT TRYPTOPHAN 64 IN ISO-1-CYTOCHROME C FROM YEASTSCHWEINGRUBER ME; STEWART JW; SHERMAN F et al.1979; J. BIOL. CHEM.; USA; DA. 1979; VOL. 254; NO 10; PP. 4132-4143; BIBL. 41 REF.Article

A MISSENSE MUTATION IN THE GENE CODING FOR RIBOSOMAL PROTEIN S17 (2PSQ) LEADING TO RIBOSOMAL ASSEMBLY DEFECTIVITY IN ESCHERICHIA COLIHERZOG A; YAGUCHI M; CABEZON T et al.1979; MOLEC. GEN. GENET.; DEU; DA. 1979; VOL. 171; NO 1; PP. 15-22; BIBL. 33 REF.Article

MUTATIONAL AMINO ACID REPLACEMENTS IN NEUROSPORA CRASSA NADP-SPECIFIC GLUTAMATE DEHYDROGENASE.BRETT M; CHAMBERS GK; HOLDER AA et al.1976; J. MOLEC. BIOL.; G.B.; DA. 1976; VOL. 106; NO 1; PP. 1-22; BIBL. 31 REF.Article

ISOLATION AND CHARACTERIZATION OF PHI X174 MUTANTS CARRYING LETHAL MISSENSE MUTATIONS IN GENE GCHAMBERS RW; KUCAN I; KUCAN Z et al.1982; NUCLEIC ACIDS RES.; ISSN 0305-1048; GBR; DA. 1982; VOL. 10; NO 20; PP. 6465-6473; BIBL. 15 REF.Article

SUPPRESSORS OF A UGG MISSENSE MUTATION IN ESCHERICHIA COLIMURGOLA EJ; CHILDRESS JR.1980; J. BACTERIOL.; USA; DA. 1980; VOL. 143; NO 1; PP. 285-292; BIBL. 18 REF.Article

ON THE DIFFERENT RESPONSE OF SALMONELLA TYPHIMURIUM HISG46 AND TA1530 TO MUTAGENIC ACTION OF BASE ANALOGUESJANION C.1979; ACTA BIOCHIM. POLON.; POL; DA. 1979; VOL. 26; NO 1-2; PP. 171-177; ABS. POL; BIBL. 17 REF.Article

CHARACTERIZATION OF MISSENSE SUPPRESSORS OF A DOUBLE MUTANT OF THE TRYPTOPHAN SYNTHETASE ALPHA CHAIN OF ESCHERICHIA COLI.MURGOLA EJ; MIMS BH; PRATHER NE et al.1978; MOLEC. GEN. GENET.; DEU; DA. 1978; VOL. 165; NO 2; PP. 225-230; BIBL. 20 REF.Article

RESTORATION OF ENZYME ACTIVITY BY RECESSIVE MISSENSE SUPPRESSORS IN THE FUNGUS COPRINUSSEALY LEWIS HM; CASSELTON LA.1978; MOLEC. GEN. GENET.; DEU; DA. 1978; VOL. 164; NO 2; PP. 211-215; BIBL. 16 REF.Article

SPONTANEOUS MISSENSE MUTATION OF AN IMMUNOGLOBULIN IN A MOUSE MYELOMA CELL LINE.KAYODE ADETUGBO; MILSTEIN C.1977; J. MOLEC. BIOL.; G.B.; DA. 1977; VOL. 115; NO 1; PP. 75-90; BIBL. 28 REF.Article

Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemiaKANNENGIESSER, Caroline; SANCHEZ, Mayka; LASCAUX, Axelle et al.Haematologica (Roma). 2011, Vol 96, Num 6, pp 808-813, issn 0390-6078, 6 p.Article

DECREASED EXPRESSION OF THE MITOCHONDRIAL MATRIX PROTEASES Lon AND CIpP IN CELLS FROM A PATIENT WITH HEREDITARY SPASTIC PARAPLEGIA (SPG13)HANSEN, J; CORYDON, T. J; PALMFELDT, J et al.Neuroscience. 2008, Vol 153, Num 2, pp 474-482, issn 0306-4522, 9 p.Article

Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesisKAPADIA, Hitesh; FRAZIER-BOWERS, Sylvia; OGAWA, Takuya et al.European journal of human genetics. 2006, Vol 14, Num 4, pp 403-409, issn 1018-4813, 7 p.Article

The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological functionPANZERI, Chris; DE PALMA, Clara; MARTINUZZI, Andrea et al.Brain. 2006, Vol 129, pp 1710-1719, issn 0006-8950, 10 p., 7Article

Detailed computational study of p53 and p16: using evolutionary sequence analysis and disease-associated mutations to predict the functional consequences of allelic variantsGREENBLATT, M. S; BEAUDET, J. G; GUMP, J. R et al.Oncogene (Basingstoke). 2003, Vol 22, Num 8, pp 1150-1163, issn 0950-9232, 14 p.Article

Resequencing and Association Analysis of the KALRN and EPHB1 Genes And Their Contribution to Schizophrenia SusceptibilityKUSHIMA, Itaru; NAKAMURA, Yukako; INADA, Toshiya et al.Schizophrenia bulletin. 2012, Vol 38, Num 3, pp 552-560, issn 0586-7614, 9 p.Article

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndromeVAN HOUDT, Jeroen K. J; NOWAKOWSKA, Beata Anna; CASTORI, Marco et al.Nature genetics. 2012, Vol 44, Num 4, pp 445-449, issn 1061-4036, 5 p.Article

Arena Syndrome Is Caused by a Missense Mutation in PLP1STEVENSON, Roger E; TARPEY, Patrick; MAY, Melanie M et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 5, pp 1081-1081, issn 1552-4825, 1 p.Article

Fibrinogen montreal : A novel missense mutation (Aα D496N) associated with hypofibrinogenaemiaSHEEN, Campbell R; BRENNAN, Stephen O; JABADO, Nada et al.Thrombosis and haemostasis. 2006, Vol 96, Num 2, pp 231-232, issn 0340-6245, 2 p.Article

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