Literature DB >> 8901413

Position effects and genetic disease.

E Milot1, P Fraser, F Grosveld.   

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Year:  1996        PMID： 8901413     DOI： 10.1016/0168-9525(96)30019-x

Source DB:  PubMed          Journal:  Trends Genet        ISSN： 0168-9525            Impact factor:   11.639


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  18 in total

1.  Mammalian linker-histone subtypes differentially affect gene expression in vivo.

Authors:  Raouf Alami; Yuhong Fan; Stephanie Pack; Timothy M Sonbuchner; Arnaud Besse; Qingcong Lin; John M Greally; Arthur I Skoultchi; Eric E Bouhassira
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-28       Impact factor: 11.205

2.  Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth.

Authors:  Luca Ferrari; Giulietta Scuvera; Arianna Tucci; Donatella Bianchessi; Francesco Rusconi; Francesca Menni; Elena Battaglioli; Donatella Milani; Paola Riva
Journal:  Hum Genet       Date:  2017-08-03       Impact factor: 4.132

3.  Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH).

Authors:  Louise V Hills; Sara Nouri; Howard R Slater
Journal:  Chromosome Res       Date:  2003       Impact factor: 5.239

Review 4.  Chimeric mice with humanized liver: tools for the study of drug metabolism, excretion, and toxicity.

Authors:  Stephen C Strom; Julio Davila; Markus Grompe
Journal:  Methods Mol Biol       Date:  2010

5.  Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.

Authors:  J M Conroy; T A Grebe; L A Becker; K Tsuchiya; R D Nicholls; K Buiting; B Horsthemke; S B Cassidy; S Schwartz
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

6.  Altered DNA-binding specificity mutants of EKLF and Sp1 show that EKLF is an activator of the beta-globin locus control region in vivo.

Authors:  N Gillemans; R Tewari; F Lindeboom; R Rottier; T de Wit; M Wijgerde; F Grosveld; S Philipsen
Journal:  Genes Dev       Date:  1998-09-15       Impact factor: 11.361

7.  46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.

Authors:  C P Venditti; N K Seese; G S Gerhard; A E Ten Elshof; K A Chorney; P N Mowrey; P G Lacey; J H Knoll; M J Chorney
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

8.  Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome.

Authors:  C J van Asperen; W C Overweg-Plandsoen; M H Cnossen; D A van Tijn; R C Hennekam
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

9.  CYP1A1 and CYP1A2 expression: comparing 'humanized' mouse lines and wild-type mice; comparing human and mouse hepatoma-derived cell lines.

Authors:  Shigeyuki Uno; Kaori Endo; Yuji Ishida; Chise Tateno; Makoto Makishima; Katsutoshi Yoshizato; Daniel W Nebert
Journal:  Toxicol Appl Pharmacol       Date:  2009-03-10       Impact factor: 4.219

10.  Independent and high-level dual-gene expression in adult stem-progenitor cells from a single lentiviral vector.

Authors:  J Tian; S T Andreadis
Journal:  Gene Ther       Date:  2009-05-14       Impact factor: 5.250
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