Slabaugh M, Cooper L, Kishore V, Knapp S, Kling J
PeerJ. 2015; 3:e915.
PMID: 26038713
PMC: 4451031.
DOI: 10.7717/peerj.915.
Kalwade S, Devarumath R
Physiol Mol Biol Plants. 2014; 20(3):313-21.
PMID: 25049458
PMC: 4101139.
DOI: 10.1007/s12298-014-0231-9.
Bodenes C, Kremer A, Laigret F
Theor Appl Genet. 2013; 93(3):348-54.
PMID: 24162290
DOI: 10.1007/BF00223175.
Zhang L, Yu Q, He J, Zha X
Mol Cell Biochem. 2004; 262(1-2):25-33.
PMID: 15532706
DOI: 10.1023/b:mcbi.0000038212.78008.7f.
Nakanishi H, Kanzaki A, Yawata A, Yamada O, Yawata Y
Int J Hematol. 2001; 73(1):54-63.
PMID: 11372755
DOI: 10.1007/BF02981903.
Characterization of beta-galactosidase mutations Asp332-->Asn and Arg148-->Ser, and a polymorphism, Ser532-->Gly, in a case of GM1 gangliosidosis.
Zhang S, Bagshaw R, Hilson W, Oho Y, Hinek A, Clarke J
Biochem J. 2000; 348 Pt 3:621-32.
PMID: 10839995
PMC: 1221106.
p53 alterations are predictive of chemoresistance and aggressiveness in ovarian carcinomas: a molecular and immunohistochemical study.
Buttitta F, Marchetti A, Gadducci A, Pellegrini S, Morganti M, Carnicelli V
Br J Cancer. 1997; 75(2):230-5.
PMID: 9010031
PMC: 2063269.
DOI: 10.1038/bjc.1997.38.
Fluorescence-based mutation detection. Single-strand conformation polymorphism analysis (F-SSCP).
Ellison J
Mol Biotechnol. 1996; 5(1):17-31.
PMID: 8853013
DOI: 10.1007/BF02762409.
Molecular analysis of patients with beta-glucuronidase deficiency presenting as hydrops fetalis or as early mucopolysaccharidosis VII.
Vervoort R, Islam M, Sly W, Zabot M, Kleijer W, Chabas A
Am J Hum Genet. 1996; 58(3):457-71.
PMID: 8644704
PMC: 1914559.
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene reveals six novel mutations.
Peral B, San Millan J, Ong A, Gamble V, Ward C, Strong C
Am J Hum Genet. 1996; 58(1):86-96.
PMID: 8554072
PMC: 1914963.
Detection of point mutations in chloroplast genes of Antirrhinum majus L. I. Identification of a point mutation in the psaB gene of a photosystem I plastome mutant.
Schaffner C, Laasch H, Hagemann R
Mol Gen Genet. 1995; 249(5):533-44.
PMID: 8544819
DOI: 10.1007/BF00290579.
Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.
Barba G, Rittner C, Schneider P
J Clin Invest. 1993; 91(4):1681-6.
PMID: 8473511
PMC: 288147.
DOI: 10.1172/JCI116377.
Excess PCR primers may dramatically affect SSCP efficiency.
Cai Q, Touitou I
Nucleic Acids Res. 1993; 21(16):3909-10.
PMID: 8367316
PMC: 309934.
DOI: 10.1093/nar/21.16.3909.
Single-strand conformation polymorphism (SSCP) analysis as a tool for genetic mapping.
Beier D
Mamm Genome. 1993; 4(11):627-31.
PMID: 8281011
DOI: 10.1007/BF00360898.
p53 mutations and overexpression in locally advanced breast cancers.
Faille A, de Cremoux P, Extra J, Linares G, Espie M, Bourstyn E
Br J Cancer. 1994; 69(6):1145-50.
PMID: 8198984
PMC: 1969448.
DOI: 10.1038/bjc.1994.225.
K-ras mutations and p53 alterations in neoplastic and nonneoplastic lesions associated with longstanding ulcerative colitis.
Chaubert P, Benhattar J, Saraga E, Costa J
Am J Pathol. 1994; 144(4):767-75.
PMID: 8160776
PMC: 1887244.
Lymphocyte responses to DR1/4 restricted peptides in rheumatoid arthritis.
Skinner M, Watson L, Geursen A, Tan P
Ann Rheum Dis. 1994; 53(3):171-7.
PMID: 8154934
PMC: 1005281.
DOI: 10.1136/ard.53.3.171.
Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): generation of a 5-cM, > 5 megabase contig on mouse chromosome 1.
Hunter K, Ontiveros S, Watson M, Stanton Jr V, Gutierrez P, Bhat D
Mamm Genome. 1994; 5(10):597-607.
PMID: 7849394
DOI: 10.1007/BF00411453.
Cholinesterase variants: rapid characterisation by PCR/SSCP and evidence for molecular homogeneity.
Hohler T, Hundt M, Rittner C, Schneider P, Meyer zum Buschenfelde K
J Med Genet. 1995; 32(2):109-12.
PMID: 7760318
PMC: 1050230.
DOI: 10.1136/jmg.32.2.109.
Heterogeneity of rice ragged stunt oryzavirus genome segment 9 and its segregation by insect vector transmission.
Suga H, UYEDA I, Yan J, Murao K, Kimura I, Tiongco E
Arch Virol. 1995; 140(8):1503-9.
PMID: 7661702
DOI: 10.1007/BF01322677.
