Literature DB >> 752535

Confirmation of the assignment of the human SODS gene to chromosome 21q22.

T Philip, J Fraisse, P M Sinet, B Lauras, J M Robert, F Freycon.   

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Year:  1978        PMID： 752535     DOI： 10.1159/000131014

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


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  9 in total

1.  Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome).

Authors:  J M Delabar; P M Sinet; B Chadefaux; A Nicole; A Gegonne; D Stehelin; F Fridlansky; N Créau-Goldberg; C Turleau; J de Grouchy
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

2.  Monosomy 21: a new case confirmed by in situ hybridization.

Authors:  M C Pellissier; N Philip; M A Voelckel-Baeteman; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

3.  Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization.

Authors:  M C Pellissier; M Laffage; N Philip; E Passage; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

4.  A case of 21q-syndrome with half normal SOD-1 activity.

Authors:  K Yoshimitsu; S Hatano; Y Kobayashi; Y Takeoka; M Hayashidani; K Ueda; K Nomura; K Ohama; T Usui
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214).

Authors:  N J Leschot; R M Slater; H Joenje; M J Becker-Bloemkolk; J J de Nef
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  MIF homolog d-dopachrome tautomerase (D-DT/MIF-2) does not inhibit accumulation and toxicity of misfolded SOD1.

Authors:  Amina Alaskarov; Shir Barel; Shamchal Bakavayev; Joy Kahn; Adrian Israelson
Journal:  Sci Rep       Date:  2022-06-10       Impact factor: 4.996

7.  Normal superoxide dismutase-1 (SOD-1) activity with deletion of chromosome band 21q21 supports localization of SOD-1 locus to 21q22.

Authors:  E A Wulfsberg; R E Carrel; I J Klisak; T J O'Brien; J A Sykes; R S Sparkes
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality.

Authors:  J L Huret; J M Delabar; F Marlhens; A Aurias; A Nicole; M Berthier; J Tanzer; P M Sinet
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

9.  Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase.

Authors:  D Levanon; J Lieman-Hurwitz; N Dafni; M Wigderson; L Sherman; Y Bernstein; Z Laver-Rudich; E Danciger; O Stein; Y Groner
Journal:  EMBO J       Date:  1985-01       Impact factor: 11.598
  9 in total

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