Literature DB >> 7327563

Evidence for the derivation of individual hair roots from three progenitor cells.

J Dancis, D N Silvers, M E Balis, R P Cox, M S Schwartz.   

Abstract

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Year:  1981        PMID： 7327563     DOI： 10.1007/bf00282826

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  7 in total

1.  SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS.

Authors:  S M GARTLER; D LINDER
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1964

2.  Detection of heterozygote in Lesch-Nyhan disease by hair-root analysis.

Authors:  D N Silvers; R P Cox; M E Balis; J Dancis
Journal:  N Engl J Med       Date:  1972-02-24       Impact factor: 91.245

3.  Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells.

Authors:  S M Gartler; E Gandini; G Angioni; N Argiolas
Journal:  Ann Hum Genet       Date:  1969-10       Impact factor: 1.670

4.  Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuria.

Authors:  J Dancis; P H Berman; V Jansen; M E Balis
Journal:  Life Sci       Date:  1968-06-15       Impact factor: 5.037

5.  Gene action in the X-chromosome of the mouse (Mus musculus L.).

Authors:  M F LYON
Journal:  Nature       Date:  1961-04-22       Impact factor: 49.962

6.  Lesch-Nyhan syndrome: rapid detection of heterozygotes by use of hair follicles.

Authors:  S M Gartler; R C Scott; J L Goldstein; B Campbell
Journal:  Science       Date:  1971-05-07       Impact factor: 47.728

7.  Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome.

Authors:  W L Nyhan; B Bakay; J D Connor; J F Marks; D K Keele
Journal:  Proc Natl Acad Sci U S A       Date:  1970-01       Impact factor: 11.205
  7 in total
  4 in total

1.  Hair root analysis in X-linked ichthyosis.

Authors:  J Dancis; V Jansen; J Hutzler
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

2.  Noninvasive test for fragile X syndrome, using hair root analysis.

Authors:  R Willemsen; B Anar; Y De Diego Otero; B B de Vries; Y Hilhorst-Hofstee; A Smits; E van Looveren; P J Willems; H Galjaard; B A Oostra
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

3.  Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopia.

Authors:  Elena Parrini; Davide Mei; Micheal Wright; Thomas Dorn; Renzo Guerrini
Journal:  Neurogenetics       Date:  2004-07-28       Impact factor: 2.660

4.  Detection of the carrier state for an X-linked disorder, the Lesch-Nyhan syndrome, by the use of lymphocyte cloning.

Authors:  J L Dempsey; A A Morley; R S Seshadri; B T Emmerson; R Gordon; C I Bhagat
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  4 in total

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