| scholarly article | Q13442814 |
| P356 | DOI | 10.1006/GENO.1993.1193 |
| P698 | PubMed publication ID | 8314571 |
| P50 | author | Edwin M. Stone | Q37381855 |
| P2093 | author name string | Val C. Sheffield | |
| Anne E. Kwitek | |||
| Dirk W. Sandstrom | |||
| John S. Beck | |||
| P433 | issue | 2 | |
| P304 | page(s) | 325-332 | |
| P577 | publication date | 1993-05-01 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions | |
| P478 | volume | 16 |
| Q52863998 | A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning. |
| Q30718645 | A decade of high-resolution liquid chromatography of nucleic acids on styrene-divinylbenzene copolymers |
| Q40983800 | A high-resolution map of the brown (b, Tyrp1) deletion complex of mouse chromosome 4. |
| Q33146682 | A malignant phenotype of hypertrophic cardiomyopathy caused by Arg719Gln cardiac beta-myosin heavy-chain mutation in a Chinese family |
| Q38335328 | A new set of primers for mutation analysis of the human PAX6 gene |
| Q24629476 | A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41 |
| Q61852823 | A rapid fluorescence based multiplex polymerase chain reaction — single-strand conformation polymorphism method forp53 mutation detection |
| Q43587195 | A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects. |
| Q56906171 | A simple method for non-radioactive PCR-SSCP using MDE gel solution and a midi gel format: application for the detection of variants in the GLUT1 and CTLA-4 genes |
| Q36222841 | A survey of the methods for the characterization of microbial consortia and communities |
| Q24676800 | Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome |
| Q37387088 | Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia |
| Q46662259 | Activation-induced cytidine deaminase expression in gastric cancer |
| Q72810544 | Acute intermittent porphyria: identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal |
| Q36620205 | Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours. |
| Q35763943 | Allelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas. |
| Q54772880 | Alpha1 and alpha2 domains of Aotus MHC class I and Catarrhini MHC class Ia share similar characteristics. |
| Q36617950 | Alteration of p16 and p15 genes in human uterine tumours |
| Q42507902 | Alterations of the insulin-like growth factor system in patients with polycythemia vera |
| Q34376745 | Altered expression of KCNK9 in colorectal cancers |
| Q61820212 | Alu repeats in the human factor IX gene: The rate of polymorphism is not substantially elevated |
| Q71131054 | An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine |
| Q38330648 | Analysis of clonal diversity in mouse immunoglobulin heavy chain genes selected for size of the antigen combining site |
| Q43803925 | Analysis of the fungal flora in environmental dust samples by PCR-SSCP method |
| Q58075201 | Analysis of the p16INK4 and TP53 tumor suppressor genes in bone sarcoma pediatric patients |
| Q78124701 | Analysis of the p53 tumor suppressor gene in rheumatoid arthritis synovial fibroblasts |
| Q24313340 | Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis |
| Q32173153 | Application of single-strand conformation polymorphism to the study of bovine viral diarrhea virus isolates |
| Q35031150 | Assessment of polymorphism in zebrafish mapping strains |
| Q42424477 | Assessment of toluene/biphenyl dioxygenase gene diversity in benzene-polluted soils: links between benzene biodegradation and genes similar to those encoding isopropylbenzene dioxygenases |
| Q33966839 | Association between SSCP haplotypes at the bovine growth hormone gene and milk protein percentage |
| Q34091682 | Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families |
| Q71913797 | Ataxia with isolated vitamin E deficiency in four siblings |
| Q34667367 | Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations |
| Q38263419 | Cell-free circulating tumor DNA in plasma/serum of non-small cell lung cancer |
| Q48086728 | Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP). |
| Q34798196 | Clinical and molecular analysis of patients with defects in micro heavy chain gene. |
| Q44353664 | Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosis |
| Q30994864 | Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection. |
| Q73111333 | Comparison of heteroduplex analysis, direct sequencing, and enzyme mismatch cleavage for detecting mutations in a large gene, FBN1 |
| Q33215293 | Comparison of near-infrared and laser-induced breakdown spectroscopy for determination of magnesium stearate in pharmaceutical powders and solid dosage forms |
| Q48359195 | Conformational SERS Classification of K-Ras Point Mutations for Cancer Diagnostics. |
| Q43110725 | Considerations in adding mutation detection services to a sequencing core facility |
| Q37135934 | Correlation of p53 over-expression and alteration in p53 gene detected by polymerase chain reaction-single strand conformation polymorphism in adenocarcinoma of gastric cancer patients from India |
| Q37364384 | Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene |
| Q36008650 | Cryptococcus gattii in AIDS patients, southern California |
| Q52007911 | Cytogenetic and p53 profiles in congenital cystic adenomatoid malformation: insights into its relationship with pleuropulmonary blastoma. |
| Q70994516 | DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia |
| Q30991032 | Denaturing high-performance liquid chromatography: A review |
| Q74618482 | Design and application of 2-D DGGE-based gene mutational scanning tests |
| Q74127887 | Detection of five novel germline mutations of the APC gene in Irish familial adenomatous polyposis families |
| Q71656273 | Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients |
| Q28138653 | Detection of mutations in the DNA polymerase delta gene of human sporadic colorectal cancers and colon cancer cell lines |
| Q48068471 | 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 |
| Q71916629 | Detection of polymorphism in the Trypanosoma cruzi TcP2 beta gene family by single strand conformational analysis (SSCA) |
| Q56893651 | Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis |
| Q58840829 | Detection of single nucleotide mutations in wheat using single strand conformation polymorphism gels |
| Q33959301 | Detection of three closely located single nucleotide polymorphisms in the EAAT2 promoter: comparison of single-strand conformational polymorphism (SSCP), pyrosequencing and Sanger sequencing |
| Q71659926 | Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutations |
| Q80773407 | Development of a simple and highly sensitive mutation screening system by enzyme mismatch cleavage with optimized conditions for standard laboratories |
| Q57588268 | Development of polymorphic EST markers in Penaeus monodon: applications in penaeid genetics |
| Q36673846 | Disruption of the MyoD/p21 Pathway in Rhabdomyosarcoma |
| Q46814393 | Dissemination and tissue invasiveness in murine acute leukemia associated with acquisition of p53 mutation and loss of wild‐type p53 |
| Q71672958 | Diversity and genetic differentiation among subpopulations of Gliricidia sepium revealed by PCR-based assays |
| Q77746239 | Downregulation of fibronectin transcription in highly metastatic adenocarcinoma cells |
| Q36620473 | E-cadherin gene mutations are rare in adenocarcinomas of the oesophagus |
| Q24540139 | EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas. |
| Q39492038 | Effect of primers hybridizing to different evolutionarily conserved regions of the small-subunit rRNA gene in PCR-based microbial community analyses and genetic profiling |
| Q73552723 | Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP |
| Q35079578 | Efficient detection of point mutations on color-coded strands of target DNA. |
| Q36393069 | Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects. |
| Q61386395 | Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families |
| Q58862180 | Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas |
| Q35882254 | Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus |
| Q53668779 | Expression of HGF/SF and Met protein is associated with genetic alterations of VHL gene in primary renal cell carcinomas. |
| Q46279688 | Fine mapping and candidate gene analysis of the virescent gene v 1 in Upland cotton (Gossypium hirsutum). |
| Q35182761 | Fine structure analysis of the WT1 gene in sporadic Wilms tumors |
| Q71644907 | Fluorescence-based mutation detection. Single-strand conformation polymorphism analysis (F-SSCP) |
| Q35840995 | Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas |
| Q30502716 | Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas |
| Q79400842 | Functional analysis of SPINDLY in gibberellin signaling in Arabidopsis |
| Q36636493 | Functional importance of complex formation between the retinoblastoma tumor suppressor family and adenovirus E1A proteins as determined by mutational analysis of E1A conserved region 2 |
| Q73189617 | G-33A mutation in the promoter region of thrombomodulin gene and its association with coronary artery disease and plasma soluble thrombomodulin levels |
| Q33599177 | Gastrointestinal polyposis syndromes |
| Q71696189 | Gene and genome scanning by two-dimensional DNA typing |
| Q34351545 | Gene therapy in glaucoma-3: Therapeutic approaches |
| Q36637441 | Gene-based approach to human gene-phenotype correlations |
| Q73934851 | Genetic alterations in gastric cancers from British patients |
| Q73746916 | Genetic alterations involving exon 3 of the beta-catenin gene do not play a role in adenocarcinomas of the esophagus |
| Q53592465 | Genetic alterations of the KLF6 gene in colorectal cancers. |
| Q53623671 | Genetic alterations of the KLF6 gene in gastric cancer. |
| Q37024483 | Genetic analysis of microsomal epoxide hydrolase gene and its association with lung cancer risk |
| Q34544116 | Genetic analysis of the LKB1/STK11 gene in hepatocellular carcinomas |
| Q40748086 | Genetic analysis of the liver putative tumor suppressor (LPTS) gene in hepatocellular carcinomas |
| Q34083049 | Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene |
| Q33566848 | Genetic aspects of familial osteoarthritis |
| Q24671452 | Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus |
| Q57009610 | Genetic differentiation between the blue and the yellow phenotypes of walleye (Sander vitreus): An example of parallel evolution |
| Q36617298 | Genetic diversity of plant virus populations: towards hypothesis testing in molecular epidemiology |
| Q33679819 | Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations. |
| Q42850964 | Genetic pathways of colorectal carcinogenesis rarely involve the PTEN and LKB1 genes outside the inherited hamartoma syndromes |
| Q47739423 | Genetic variation in the amino-terminal part of apolipoprotein B: studies in hyperlipidemic patients |
| Q28240992 | Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuria |
| Q34384437 | Germ-line mutational analysis of the TSC2 gene in 90 tuberous-sclerosis patients |
| Q36431527 | Germline BRCA2 mutations in men with breast cancer |
| Q42005199 | Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer |
| Q46549319 | Glucokinase gene in gestational diabetes mellitus: population association study and molecular scanning |
| Q33578883 | HLA class I associations of ankylosing spondylitis in the white population in the United Kingdom. |
| Q48154517 | High frequency of TP53 mutations in juvenile pilocytic astrocytomas indicates role of TP53 in the development of these tumors |
| Q57807288 | High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method |
| Q57807348 | High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants |
| Q34390891 | Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion |
| Q44334554 | Human mu opioid receptor gene polymorphisms and vulnerability to substance abuse. |
| Q28205793 | Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder |
| Q61863688 | Identification and characterisation of polymorphisms in the promoter region of the human Apo-1/Fas (CD95) gene |
| Q28211939 | Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients |
| Q78116286 | Identification of X-linked severe combined immunodeficiency by mutation analysis of blood and hair roots |
| Q24539167 | Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations |
| Q28619897 | Identification of genetic variants in the human thromboxane synthase gene (CYP5A1) |
| Q71636662 | Identification of three novel mutations in the CFTR gene using temperature-optimized non-radioactive conditions for SSCP analysis |
| Q47779992 | Imbalance of G and C contents influences the sensitivity of single-strand conformation polymorphism. |
| Q33288615 | Improvements of polymerase chain reaction and capillary electrophoresis single-strand conformation polymorphism methods in microbial ecology: toward a high-throughput method for microbial diversity studies in soil |
| Q45883589 | Inconsistent genetic structure among members of a multitrophic system: did bruchid parasitoids (Horismenus spp.) escape the effects of bean domestication? |
| Q40070013 | Infrequent alterations of the APC and MCC genes in gastric cancers from British patients |
| Q42560736 | Infrequent mutation of the tumour-suppressor gene Smad4 in early-stage colorectal cancer. |
| Q58298619 | Infrequent mutation of theWT1 gene in 77 Wilms' tumors |
| Q60441340 | Inheritance and molecular variations of PCR-SSCP fragments in pedunculate oak (Quercus robur L.) |
| Q57179383 | Intra- and intersporal diversity of ITS rDNA sequences in Glomus intraradices assessed by cloning and sequencing, and by SSCP analysis |
| Q27489519 | Is Single-Strand Conformation Polymorphism Analysis of the Full 5' Untranslated Region an Adequate Approach To Study Hepatitis C Virus Quasispecies Distribution? |
| Q56777888 | Is there any correlation between the elevated plasma levels and gene variations of factor VIII in Turkish thrombosis patients? |
| Q45886786 | Isolation and characterization of thymitaq (AG337) and 5-fluoro-2-deoxyuridylate-resistant mutants of human thymidylate synthase from ethyl methanesulfonate-exposed human sarcoma HT1080 cells |
| Q24683595 | Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes |
| Q73591285 | Karyotypic abnormalities associated with haemopoietic lineage switching are not linked with mutations to p53 |
| Q61695497 | Leptin level and structure in Italian obese children |
| Q35750063 | Linkage between obesity and a marker near the tumor necrosis factor-alpha locus in Pima Indians |
| Q30978613 | Linkage disequilibrium analysis of case-control data: an application to generalized aggressive periodontitis |
| Q34384452 | Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p. |
| Q36080231 | Loss of heterozygosity on chromosome 22 in ovarian carcinoma is distal to and is not accompanied by mutations in NF2 at 22q12. |
| Q74449555 | Low density lipoprotein receptor mutations in a selected population of individuals with moderate hypercholesterolemia |
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| Q73215482 | Maternal and paternal lineages of the Samaritan isolate: mutation rates and time to most recent common male ancestor |
| Q28145264 | Methylation-sensitive, single-strand conformation analysis (MS-SSCA): A rapid method to screen for and analyze methylation |
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| Q77357835 | Molecular genetic analysis of the von Hippel-Lindau and human peroxisome proliferator-activated receptor gamma tumor-suppressor genes in adenocarcinomas of the gastroesophageal junction |
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| Q24672071 | Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal |
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