Pages that link to "Q67432394"
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The following pages link to Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1 (Q67432394):
Displaying 50 items.
- The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17 (Q24679421) (← links)
- Oxidative stress, thyroid dysfunction & Down syndrome (Q26782125) (← links)
- Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody (Q28285202) (← links)
- Assignment of the gene for cytoplasmic superoxide dismutase ( Sod-1 ) to a region of chromosome 16 and of Hprt to a region of the X chromosome in the mouse (Q28511445) (← links)
- Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16. (Q33588304) (← links)
- De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome (Q33594571) (← links)
- Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17 (Q33640527) (← links)
- Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother. (Q33667884) (← links)
- Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation (Q33669486) (← links)
- A case of partial monosomy 21q22.2 associated with Rieger's syndrome. (Q33671381) (← links)
- Molecular genetics of human chromosome 21. (Q33674852) (← links)
- Partial deletion 21: case report with biochemical studies and review (Q33676280) (← links)
- Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions (Q33916503) (← links)
- A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21. (Q33931702) (← links)
- Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality (Q34048454) (← links)
- Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype (Q34172804) (← links)
- Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome (Q34294835) (← links)
- Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34. (Q34769077) (← links)
- Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21. (Q35197932) (← links)
- Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids (Q35200986) (← links)
- Dosage effects for superoxide dismutase-1 in nucleated cells aneuploid for chromosome 21 (Q35202613) (← links)
- Inversion duplication of chromosome 6 with trisomic codominant expression of HLA antigens (Q35202933) (← links)
- Demonstration, by somatic cell genetics, of coordinate regulation of genes for two enzymes of purine synthesis assigned to human chromosome 21. (Q35308594) (← links)
- Comparative map for mice and humans (Q35364327) (← links)
- Human cytoplasmic superoxide dismutase cDNA clone: a probe for studying the molecular biology of Down syndrome (Q36293605) (← links)
- Genes coding for sensitivity to interferon (IfRec) and soluble superoxide dismutase (SOD-1) are linked in mouse and man and map to mouse chromosome 16 (Q36364578) (← links)
- Visualization of the conservation of synteny between humans and pigs by heterologous chromosomal painting (Q36686356) (← links)
- Nucleotide sequence and expression of human chromosome 21-encoded superoxide dismutase mRNA. (Q37348330) (← links)
- Isolation and analysis of the 21q+ chromosome in the acute myelogenous leukemia 8;21 translocation: evidence that c-mos is not translocated (Q37674846) (← links)
- The estimation of red cell superoxide dismutase activity by pulse radiolysis in normal and trisomic 21 subjects (Q39791952) (← links)
- Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype (Q39828341) (← links)
- Trisomy 21 (Down's Syndrome) glutathione peroxidase, hexose monophosphate shunt and I.Q (Q39875081) (← links)
- Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21) (Q39893526) (← links)
- Null mutants of Saccharomyces cerevisiae Cu,Zn superoxide dismutase: characterization and spontaneous mutation rates (Q39943252) (← links)
- Functional Implications of Gene Dosage Effects in Trisomy 21 (Q40105588) (← links)
- Structural Variation of Chromosome 21 and Symptoms of Down’s Syndrome (Q40114083) (← links)
- Down syndrome—a disruption of homeostasis (Q40114490) (← links)
- Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies (Q40203998) (← links)
- Human Cu/Zn superoxide dismutase gene: molecular characterization of its two mRNA species (Q40463376) (← links)
- Anatomical analysis of the developmental effects of aneuploidy in man—the 18-trisomy syndrome: II. Anomalies of the upper and lower limbs (Q40468527) (← links)
- Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase. (Q41378091) (← links)
- A case of 21q-syndrome with normal SOD-1 activity (Q41737084) (← links)
- Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the down syndrome (Q41934361) (← links)
- Duplication 15q22�15qter and its phenotypic expression (Q41935691) (← links)
- Copper/zinc superoxide dismutase (SOD-1) activity in regular trisomy 21, trisomy 21 by translocation and mosaic trisomy 21 (Q43456927) (← links)
- Localization and quantitation of human superoxide dismutase using computerized 2-D gel electrophoresis (Q43579790) (← links)
- Systematic analysis of 95 reciprocal translocations of autosomes (Q44997574) (← links)
- Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization (Q45227605) (← links)
- Copper/zinc superoxide dismutase activity in trisomy 21 by translocation (Q45354328) (← links)
- Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion (Q46301621) (← links)