Literature DB >> 8054969

Unequal expression of NF1 alleles.

S Hoffmeyer, G Assum, D Kaufmann, W Krone.   

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Year:  1994        PMID： 8054969     DOI： 10.1038/ng0494-331

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  10 in total

1.  Unequal expression of allelic kainate receptor GluR7 mRNAs in human brains.

Authors:  H H Schiffer; G T Swanson; E Masliah; S F Heinemann
Journal:  J Neurosci       Date:  2000-12-15       Impact factor: 6.167

2.  Differential allelic expression of lactoproteins: a model to study transcriptional regulation.

Authors:  P Dovc; L Lum; J F Medrano
Journal:  Pflugers Arch       Date:  1996       Impact factor: 3.657

3.  Nearby stop codons in exons of the neurofibromatosis type 1 gene are disparate splice effectors.

Authors:  S Hoffmeyer; P Nürnberg; H Ritter; R Fahsold; W Leistner; D Kaufmann; W Krone
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

Review 4.  Molecular genetics of neurofibromatosis type 1 (NF1).

Authors:  M H Shen; P S Harper; M Upadhyaya
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

5.  Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency.

Authors:  E L Aronovich; D Pan; C B Whitley
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

6.  Increased noise as an effect of haploinsufficiency of the tumor-suppressor gene neurofibromatosis type 1 in vitro.

Authors:  Ralf Kemkemer; Stephanie Schrank; Walther Vogel; Hans Gruler; Dieter Kaufmann
Journal:  Proc Natl Acad Sci U S A       Date:  2002-10-04       Impact factor: 11.205

7.  A Tsp509I variant in exon 13 of the neurofibromatosis type 1 (NF1) gene allows the identification of both alleles at the mRNA level.

Authors:  V Régnier; G Danglot; V C Nguyen; A Bernheim
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

8.  Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism.

Authors:  C Lázaro; A Gaona; M Lynch; H Kruyer; A Ravella; X Estivill
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

9.  Faster cross-bridge detachment and increased tension cost in human hypertrophic cardiomyopathy with the R403Q MYH7 mutation.

Authors:  E Rosalie Witjas-Paalberends; Claudia Ferrara; Beatrice Scellini; Nicoletta Piroddi; Judith Montag; Chiara Tesi; Ger J M Stienen; Michelle Michels; Carolyn Y Ho; Theresia Kraft; Corrado Poggesi; Jolanda van der Velden
Journal:  J Physiol       Date:  2014-06-13       Impact factor: 5.182

10.  Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.

Authors:  Snigdha Tripathi; Imke Schultz; Edgar Becker; Judith Montag; Bianca Borchert; Antonio Francino; Francisco Navarro-Lopez; Andreas Perrot; Cemil Özcelik; Karl-Josef Osterziel; William J McKenna; Bernhard Brenner; Theresia Kraft
Journal:  Basic Res Cardiol       Date:  2011-07-19       Impact factor: 17.165
  10 in total

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