Literature DB >> 7103411

Linkage between dentinogenesis imperfecta and Gc.

S P Ball, P J Cook, M Mars, K E Buckton.   

Abstract

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Year:  1982        PMID： 7103411     DOI： 10.1111/j.1469-1809.1982.tb00693.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  11 in total

1.  Evolutionary and structural relationships among the group-specific component, albumin and alpha-fetoprotein.

Authors:  F Yang; V J Luna; R D McAnelly; K H Naberhaus; R L Cupples; B H Bowman
Journal:  Nucleic Acids Res       Date:  1985-11-25       Impact factor: 16.971

2.  Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III.

Authors:  M MacDougall; M Zeichner-David; J Murray; M Crall; A Davis; H Slavkin
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

3.  Localization of the human c-kit protooncogene on the q11-q12 region of chromosome 4.

Authors:  L d'Auriol; M G Mattei; C Andre; F Galibert
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

4.  Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAs.

Authors:  J C vanderSpek; H E Wyandt; J C Skare; A Milunsky; F G Oppenheim; R F Troxler
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

5.  Pairwise linkage analysis of 11 loci on human chromosome 4.

Authors:  J C Murray; K H Buetow; M Smith; L Carlock; A Chakravarti; R F Ferrell; L Gedamu; C Gilliam; R Shiang; C R DeHaven
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

6.  Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP.

Authors:  Zofia von Marschall; Seeun Mok; Matthew D Phillips; Dianalee A McKnight; Larry W Fisher
Journal:  J Bone Miner Res       Date:  2012-06       Impact factor: 6.741

7.  Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism.

Authors:  N E Cooke; H F Willard; E V David; D L George
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

8.  Human group-specific component (Gc) is a member of the albumin family.

Authors:  F Yang; J L Brune; S L Naylor; R L Cupples; K H Naberhaus; B H Bowman
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

9.  Genetic mapping of the dentinogenesis imperfecta type II locus.

Authors:  A H Crosby; T Scherpbier-Heddema; C Wijmenga; M R Altherr; J C Murray; K H Buetow; M J Dixon
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

10.  A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene.

Authors:  Dianalee A McKnight; P Suzanne Hart; Thomas C Hart; James K Hartsfield; Anne Wilson; J Timothy Wright; Larry W Fisher
Journal:  Hum Mutat       Date:  2008-12       Impact factor: 4.878
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