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Literature DB >> 8178814

New insights reveal complex mechanisms involved in genomic imprinting.

R D Nicholls¹.

Abstract

Mesh：

Year: 1994 PMID： 8178814 PMCID： PMC1918270

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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51 in total

1. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

Authors: R D Nicholls; J H Knoll; M G Butler; S Karam; M Lalande
Journal: Nature Date: 1989-11-16 Impact factor: 49.962

Review 2. Genomic imprinting: review and relevance to human diseases.

Authors: J G Hall
Journal: Am J Hum Genet Date: 1990-05 Impact factor: 11.025

3. Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Authors: A Reis; B Dittrich; V Greger; K Buiting; M Lalande; G Gillessen-Kaesbach; M Anvret; B Horsthemke
Journal: Am J Hum Genet Date: 1994-05 Impact factor: 11.025

4. Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.

Authors: J Wagstaff; J H Knoll; K A Glatt; Y Y Shugart; A Sommer; M Lalande
Journal: Nat Genet Date: 1992-07 Impact factor: 38.330

5. Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2.

Authors: S Zemel; M S Bartolomei; S M Tilghman
Journal: Nat Genet Date: 1992-09 Impact factor: 38.330

6. Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome.

Authors: M L Reed; S E Leff
Journal: Nat Genet Date: 1994-02 Impact factor: 38.330

7. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.

Authors: J H Knoll; S D Cheng; M Lalande
Journal: Nat Genet Date: 1994-01 Impact factor: 38.330

8. Functional imprinting and epigenetic modification of the human SNRPN gene.

Authors: C C Glenn; K A Porter; M T Jong; R D Nicholls; D J Driscoll
Journal: Hum Mol Genet Date: 1993-12 Impact factor: 6.150

9. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

Authors: M Nakao; J S Sutcliffe; B Durtschi; A Mutirangura; D H Ledbetter; A L Beaudet
Journal: Hum Mol Genet Date: 1994-02 Impact factor: 6.150

10. Rescue of the T-associated maternal effect in mice carrying null mutations in Igf-2 and Igf2r, two reciprocally imprinted genes.

Authors: A J Filson; A Louvi; A Efstratiadis; E J Robertson
Journal: Development Date: 1993-07 Impact factor: 6.868

29 in total

1. Dynamic methylation adjustment and counting as part of imprinting mechanisms.

Authors: R Shemer; Y Birger; W L Dean; W Reik; A D Riggs; A Razin
Journal: Proc Natl Acad Sci U S A Date: 1996-06-25 Impact factor: 11.205

2. The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.

Authors: S Toth-Fejel; S Olson; K Gunter; F Quan; J Wolford; B W Popovich; R E Magenis
Journal: Am J Hum Genet Date: 1996-05 Impact factor: 11.025

3. The mechanisms involved in formation of deletions and duplications of 15q11-q13.

Authors: W P Robinson; F Dutly; R D Nicholls; F Bernasconi; M Peñaherrera; R C Michaelis; D Abeliovich; A A Schinzel
Journal: J Med Genet Date: 1998-02 Impact factor: 6.318

4. Molecular diagnosis of Prader-Willi syndrome: comparison of cytogenetic and molecular genetic data including parent of origin dependent methylation DNA patterns.

Authors: M G Butler
Journal: Am J Med Genet Date: 1996-01-11