Literature DB >> 8062592

Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994.

N C Dracopoli1, G A Bruns, G M Brodeur, G M Landes, T C Matise, M F Seldin, J M Vance, A Weith.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 8062592

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  11 in total

1.  Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.

Authors:  C Williamson; A A Pannett; J T Pang; C Wooding; M McCarthy; M N Sheppard; J Monson; R N Clayton; R V Thakker
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

Review 2.  Receptor-like protein tyrosine phosphatases: alike and yet so different.

Authors:  R Schaapveld; B Wieringa; W Hendriks
Journal:  Mol Biol Rep       Date:  1997-11       Impact factor: 2.316

Review 3.  DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.

Authors:  S Knuutila; A M Björkqvist; K Autio; M Tarkkanen; M Wolf; O Monni; J Szymanska; M L Larramendy; J Tapper; H Pere; W El-Rifai; S Hemmer; V M Wasenius; V Vidgren; Y Zhu
Journal:  Am J Pathol       Date:  1998-05       Impact factor: 4.307

4.  Duplication of seven exons in the lysyl hydroxylase gene is associated with longer forms of a repetitive sequence within the gene and is a common cause for the type VI variant of Ehlers-Danlos syndrome.

Authors:  J Heikkinen; T Toppinen; H Yeowell; T Krieg; B Steinmann; K I Kivirikko; R Myllylä
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

5.  A tightly organized, conserved gene cluster on mouse chromosome 3 (E3-F1).

Authors:  H L Vos; M Mockensturm-Wilson; P M Rood; A M Maas; T Duhig; S J Gendler; P Bornstein
Journal:  Mamm Genome       Date:  1995-11       Impact factor: 2.957

6.  Investigation of genetic alterations associated with development and adverse outcome in patients with astrocytic tumor.

Authors:  A M Cianciulli; E Morace; A M Coletta; E Occhipinti; G M Gandolfo; G Leonardo; C M Carapella
Journal:  J Neurooncol       Date:  2000-06       Impact factor: 4.130

7.  Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients.

Authors:  F Rinaldi; A Botta; L Vallo; G Contino; A Morgante; R Iraci; C Catalli; G Silvestri; V M Ventriglia; L Politano; G Novelli
Journal:  Acta Myol       Date:  2008-12

8.  A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.

Authors:  P S White; J M Maris; C Beltinger; E Sulman; H N Marshall; M Fujimori; B A Kaufman; J A Biegel; C Allen; C Hilliard; M B Valentine; A T Look; H Enomoto; S Sakiyama; G M Brodeur
Journal:  Proc Natl Acad Sci U S A       Date:  1995-06-06       Impact factor: 11.205

9.  RAD18 and poly(ADP-ribose) polymerase independently suppress the access of nonhomologous end joining to double-strand breaks and facilitate homologous recombination-mediated repair.

Authors:  Alihossein Saberi; Helfrid Hochegger; David Szuts; Li Lan; Akira Yasui; Julian E Sale; Yoshihito Taniguchi; Yasuhiro Murakawa; Weihua Zeng; Kyoko Yokomori; Thomas Helleday; Hirobumi Teraoka; Hiroshi Arakawa; Jean-Marie Buerstedde; Shunichi Takeda
Journal:  Mol Cell Biol       Date:  2007-01-22       Impact factor: 4.272

10.  Deletion mapping on chromosome 1p in well-differentiated gastric cancer.

Authors:  T Ezaki; A Yanagisawa; K Ohta; S Aiso; M Watanabe; T Hibi; Y Kato; T Nakajima; T Ariyama; J Inazawa; Y Nakamura; A Horii
Journal:  Br J Cancer       Date:  1996-02       Impact factor: 7.640
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