A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies.
about
The flavin-containing monooxygenase 2 gene (FMO2) of humans, but not of other primates, encodes a truncated, nonfunctional proteinThe geographic distribution of human Y chromosome variationFounder mutations in the BRCA1 gene in Polish families with breast-ovarian cancerMAOA methylation is associated with nicotine and alcohol dependence in women.The relationship of 5HTT (SLC6A4) methylation and genotype on mRNA expression and liability to major depression and alcohol dependence in subjects from the Iowa Adoption StudiesGenetic signatures of parental contribution in black and white populations in BrazilFamilial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14A new genetic locus for X linked progressive cone-rod dystrophyAssociation study of polymorphisms in the excitatory amino acid transporter 2 gene (SLC1A2) with schizophreniaATR mutation in endometrioid endometrial cancer is associated with poor clinical outcomes.Family-based association study of 5-HTTLPR, TPH, MAO-A, and DRD4 polymorphisms in mood disordersPharmacogenetics of lithium prophylaxis in mood disorders: analysis of COMT, MAO-A, and Gbeta3 variantsAssociation of CYP7A1 -278A>C polymorphism and the response of plasma triglyceride after dietary intervention in dyslipidemic patientsc.194 A>C (Q65P) mutation in the LMX1B gene in patients with nail-patella syndrome associated with glaucomaVariants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autismDetection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastomaNo association between mean telomere length and life stress observed in a 30 year birth cohortAssociation of the Myostatin gene with obesity, abdominal obesity and low lean body mass and in non-diabetic Asian Indians in north IndiaGST M1-T1 null allele frequency patterns in geographically assorted human populations: a phylogenetic approachEvaluation of Psoriasis Genetic Risk Based on Five Susceptibility Markers in a Population from Northern PolandFGFR2 point mutations in 466 endometrioid endometrial tumors: relationship with MSI, KRAS, PIK3CA, CTNNB1 mutations and clinicopathological featuresChromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility geneIdentification of a novel gene on chromosome 13 between BRCA-2 and RB-1.Serine racemase is associated with schizophrenia susceptibility in humans and in a mouse model.Development and validation of the high-quality 'rapid method for swab' to genotype the HTTLPR serotonin transporter (SLC6A4) promoter polymorphism.Examination of the nicotine dependence (NICSNP) consortium findings in the Iowa adoption studies population.The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and languageThe association between the SLC6A3 VNTR 9-repeat allele and alcoholism-a meta-analysis.Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutationAngiotensin converting enzyme (ACE) gene expression in the human left ventricle: effect of ACE gene insertion/deletion polymorphism and left ventricular function.Genotypic and phenotypic progression in endometrial tumorigenesis: determining when defects in DNA mismatch repair and KRAS2 occur.Association between the Catechol O-methyltransferase (COMT) Val158met polymorphism and different dimensions of impulsivity.Molecular basis of beta-thalassemia in the Maldives.AIB1 gene amplification and the instability of polyQ encoding sequence in breast cancer cell lines.An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians.Association study of polymorphisms in the neutral amino acid transporter genes SLC1A4, SLC1A5 and the glycine transporter genes SLC6A5, SLC6A9 with schizophrenia.Genetic association study of selected candidate genes (ApoB, LPL, Leptin) and telomere length in obese and hypertensive individuals.Telomere length in human adults and high level natural background radiationMutations in the coding regions of the hepatocyte nuclear factor 4 alpha in Iranian families with maturity onset diabetes of the youngCOMT polymorphism influences decrease of ovarian follicles and emerges as a predictive factor for premature ovarian insufficiency
P2860
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P2860
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh
1991年學術文章
@zh-hant
name
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies.
@en
type
label
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies.
@en
prefLabel
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies.
@en
P356
P1476
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies.
@en
P2093
P2860
P356
10.1093/NAR/19.19.5444
P577
1991-10-01T00:00:00Z