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Abbreviation : ACRS
Long Form : amplification-created restriction site
No. Year Title Co-occurring Abbreviation
2019 Rapid and easy detection of the five most common mutations in BRCA1 and BRCA2 genes in the Polish population using CAPS and ACRS-PCR methods. CAPS
2013 Mutation spectrum of phenylketonuria in Syrian population: genotype-phenotype correlation. PAH, PKU, RFLP
2011 Analysis of the CYP21A1P pseudogene: indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes. PCR
2009 A simple PCR-based genotyping method for M105I mutation of alpha-SNAP enhances the study of early pathological changes in hyh phenotype. PCR
2008 Tests for the measurement of factor VII-activating protease (FSAP) activity and antigen levels in citrated plasma, their correlation to PCR testing, and utility for the detection of the Marburg I-polymorphism of FSAP. CV, FSAP, MRI
2007 Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test. ARMS, BI-PASA, WD
2006 A novel accurate ACRS-PCR method with a digestion internal control for identification of wild type and YMDD mutants of hepatitis B virus strains. HBV
2006 [Detection of the prevalent mutations of 6-pyruvoyl-tetrahydropterin synthase gene by PCR-RFLP analysis in Chinese patients]. PCR-RFLP, PTPS, PTPSD
2005 A novel accurate amplification created restriction site method for determination of the wild type and the precore mutant hepatitis B virus variants. HBV
10  2005 The implication of de novo 21-hydroxylase mutation in clinical and prenatal molecular diagnoses. PCR, RFLP, STR
11  2003 Molecular identification of combined homozygous and compound heterozygous mutations in the CYP21 gene in simple virilizing congenital adrenal hyperplasia in Taiwan. CAH, PCR, SSCP
12  2003 Rapid detection methods for five HGO gene mutations causing alkaptonuria. AKU, ARMS
13  2003 [CYP21 gene point mutations study in 21-hydroxylase deficiency patients]. CAH, PCR, RFLP
14  2002 Prenatal diagnosis of 21-hydroxylase deficiency caused by gene conversion and rearrangements: pitfalls and molecular diagnostic solutions. ASO, CAH, PCR
15  2001 A novel mis-sense mutation (G1381A) in the G6PD gene identified in a Chinese man. ARMS, G6PD, NBT, SSCP
16  2001 Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency. CAH, PCR
17  2001 [Five de novo forms of polymorphisms first found in Chinese mitochondrial genome]. ---
18  2000 A novel PCR-RFLP assay for the detection of a polymorphism in the 3' of STAT6 gene. ---
19  2000 [Spectrum and methods of detection of mutations in a phenylalanine hydroxylase gene from patients with phenylketonuria from the Novosibirsk region]. DGGE, PKU, RFLP
20  1998 A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease. EDNRA, EDNRB, HSCR, LWFS
21  1998 Congenital adrenal hyperplasia. Molecular characterization. CAH, CD, I236N, NC, PCR, SV, SW
22  1997 Investigation of the Met-267 Arg exchange in isoform 1 of the human plasma membrane calcium pump in patients with essential hypertension by the amplification-created restriction site technique. Arg, Met
23  1997 Prenatal diagnosis of thalassemia in the Chinese. Hb, SEA
24  1997 Rapid screening method for detecting mutations in the 21-hydroxylase gene. ---
25  1996 Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia. CAH, PCR
26  1996 Prenatal and molecular diagnosis of hemophilia B. FIX
27  1995 A simple method to detect the RYR1 mutation G1021A, a cause of malignant hyperthermia susceptibility. MH, SSCP
28  1995 Rapid detection of hemoglobin variants by mutagenically separated polymerase chain reaction (MS-PCR). Hb CS, MS-PCR
29  1994 Prenatal diagnosis of beta-thalassemic mutations in Chinese by multiple restriction fragment-single strand conformation polymorphism analysis. MRF, PCR, SSCP
30  1994 Rapid detection of -alpha 4.2 deletion of alpha-thalassemia-2 by polymerase chain reaction. ARMS
31  1993 New strategy for detection of ALDH2 mutant. ---
32  1993 Prenatal and molecular diagnosis of beta-thalassemia major in Taiwan by naturally and amplified created restriction sites. BMT
33  1992 Detection of multiple beta-casein (CASB) alleles by amplification created restriction sites (ACRS). CASB, PCR