Literature DB >> 2813076

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood.

J Grimberg1, S Nawoschik, L Belluscio, R McKee, A Turck, A Eisenberg.   

Abstract

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Year:  1989        PMID: 2813076      PMCID: PMC334995          DOI: 10.1093/nar/17.20.8390

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


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  3 in total

1.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

2.  A rapid method for the purification of DNA from blood.

Authors:  M Jeanpierre
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

3.  A simple, rapid, and sensitive DNA assay procedure.

Authors:  C Labarca; K Paigen
Journal:  Anal Biochem       Date:  1980-03-01       Impact factor: 3.365

  3 in total
  172 in total

1.  A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Authors:  K Fukushima; N Kasai; Y Ueki; K Nishizaki; K Sugata; S Hirakawa; A Masuda; M Gunduz; Y Ninomiya; Y Masuda; M Sato; W T McGuirt; P Coucke; G Van Camp; R J Smith
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Fine mapping of progressive pseudorheumatoid dysplasia: a tool for heterozygote identification.

Authors:  A Alkhateeb; J al-Alami; S M Leal; H el-Shanti; A Alkbateeb
Journal:  Genet Test       Date:  1999

3.  Efficient recovery of DNA from peripheral blood for diagnostic analysis with a vacuum manifold.

Authors:  S M Kukuczka; L E Grosso
Journal:  Mol Diagn       Date:  2000-06

Review 4.  Human identity testing with PCR-based systems.

Authors:  C Hohoff; B Brinkmann
Journal:  Mol Biotechnol       Date:  1999-12-01       Impact factor: 2.695

5.  Mutations in FYCO1 cause autosomal-recessive congenital cataracts.

Authors:  Jianjun Chen; Zhiwei Ma; Xiaodong Jiao; Robert Fariss; Wanda Lee Kantorow; Marc Kantorow; Eran Pras; Moshe Frydman; Elon Pras; Sheikh Riazuddin; S Amer Riazuddin; J Fielding Hejtmancik
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6.  Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

Authors:  J M Bork; L M Peters; S Riazuddin; S L Bernstein; Z M Ahmed; S L Ness; R Polomeno; A Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Z Ahmed; S N Khan; V M Kaloustian; X C Li; A Lalwani; S Riazuddin; M Bitner-Glindzicz; W E Nance; X Z Liu; G Wistow; R J Smith; A J Griffith; E R Wilcox; T B Friedman; R J Morell
Journal:  Am J Hum Genet       Date:  2000-11-21       Impact factor: 11.025

7.  Comparison of genomic DNA extraction techniques from whole blood samples: a time, cost and quality evaluation study.

Authors:  Diego Chacon-Cortes; Larisa M Haupt; Rod A Lea; Lyn R Griffiths
Journal:  Mol Biol Rep       Date:  2012-01-07       Impact factor: 2.316

8.  The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23.

Authors:  G Ali; R L P Santos; P John; M A L Wambangco; K Lee; W Ahmad; Sm Leal
Journal:  Clin Genet       Date:  2006-05       Impact factor: 4.438

9.  DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.

Authors:  Muhammad Wajid; Amir Ali Abbasi; Muhammad Ansar; Thanh L Pham; Kai Yan; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
Journal:  Eur J Hum Genet       Date:  2003-10       Impact factor: 4.246

10.  Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation chi-square (MASC) method: rejection of the unifying-shared-epitope hypothesis.

Authors:  M H Dizier; J F Eliaou; M C Babron; B Combe; J Sany; J Clot; F Clerget-Darpoux
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

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