Pages that link to "Q34162954"

The following pages link to Complete sequence and structure of the gene for human adenosine deaminase (Q34162954):

Displaying 50 items.

• The human homolog of insect-derived growth factor, CECR1, is a candidate gene for features of cat eye syndrome (Q22253858) (← links)
• Four new adenosine deaminase mutations, altering a zinc-binding histidine, two conserved alanines, and a 5′ splice site (Q24317069) (← links)
• Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles (Q24539210) (← links)
• Genomic structure and chromosomal localization of the human deoxycytidine kinase gene (Q24563825) (← links)
• Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency (Q24627783) (← links)
• Molecular analysis of mutations in a patient with purine nucleoside phosphorylase deficiency (Q24669781) (← links)
• Effect of genetic factors on the association between coronary artery disease and PTPN22 polymorphism (Q27009002) (← links)
• Mutations in the human adenosine deaminase gene that affect protein structure and RNA splicing (Q30405040) (← links)
• Adenosine deaminase: functional implications and different classes of inhibitors (Q32063453) (← links)
• Molecular organization of the human Raf-1 promoter region (Q33255737) (← links)
• Hot spot mutations in adenosine deaminase deficiency (Q33740382) (← links)
• Improved gene expression upon transfer of the adenosine deaminase minigene outside the transcriptional unit of a retroviral vector (Q33856071) (← links)
• Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype (Q33907756) (← links)
• Adenosine deaminase deficiency as the first target disorder in gene therapy (Q34074759) (← links)
• Novel families of interspersed repetitive elements from the human genome (Q34149014) (← links)
• Genotype is an important determinant of phenotype in adenosine deaminase deficiency (Q34263693) (← links)
• Retroviral vector-mediated high-efficiency expression of adenosine deaminase (ADA) in hematopoietic long-term cultures of ADA-deficient marrow cells (Q34301777) (← links)
• Cell surface adenosine deaminase: much more than an ectoenzyme. (Q34434639) (← links)
• Severe combined immune deficiency due to a homozygous 3.2-kb deletion spanning the promoter and first exon of the adenosine deaminase gene (Q34723162) (← links)
• Sp1 is essential for both enhancer-mediated and basal activation of the TATA-less human adenosine deaminase promoter (Q34806706) (← links)
• Efficient selection of 3'-terminal exons from vertebrate DNA. (Q35020287) (← links)
• Recombination mediates production of an extrachromosomal circular DNA containing a transposon-like human element, THE-1 (Q35161984) (← links)
• Homozygosity for a newly identified missense mutation in a patient with very severe combined immunodeficiency due to adenosine deaminase deficiency (ADA-SCID) (Q35196912) (← links)
• A high proportion of ADA point mutations associated with a specific alanine-to-valine substitution (Q35197366) (← links)
• Identification and characterization of nine RFLPs at the adenosine deaminase (ADA) locus (Q35248529) (← links)
• Dancing with Complement C4 and the RP-C4-CYP21-TNX (RCCX) Modules of the Major Histocompatibility Complex (Q35578276) (← links)
• Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements (Q35587356) (← links)
• Cell type-specific transcriptional regulation of the human adenosine deaminase gene (Q35864934) (← links)
• 1995 William Allan Award address. Human genetics: a discipline at risk for fragmentation (Q35882478) (← links)
• Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery (Q35889300) (← links)
• Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiency. (Q35889409) (← links)
• The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA (Q35907237) (← links)
• Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes (Q36728551) (← links)
• Expression of human adenosine deaminase in murine hematopoietic cells (Q36849892) (← links)
• The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome (Q37737988) (← links)
• The map of chromosome 20. (Q39568169) (← links)
• Adenosine deaminase mRNA expression is regulated posttranscriptionally during differentiation of HL-60 cells (Q40389773) (← links)
• Adenosine deaminase deficiency: molecular basis and recent developments (Q40411058) (← links)
• The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA. (Q40448133) (← links)
• An STS in the human adenosine deaminase gene (located 20q12-q13.11) (Q40507144) (← links)
• Detection of Pstl RFLP in human ADA by the polymerase chain reaction (Q40507718) (← links)
• Human transposon-like elements insert at a preferred target site: evidence for a retrovirally mediated process (Q40537128) (← links)
• Association of G22A and A4223C ADA1 gene polymorphisms and ADA activity with PCOS. (Q40852075) (← links)
• Disruption of the adenosine deaminase (ADA) gene using a dicistronic promoterless construct: Production of an ADA-deficient homozygote ES cell line (Q41329252) (← links)
• Clinical expression, genetics and therapy of adenosine deaminase (ADA) deficiency (Q41521392) (← links)
• Enzymatic and extraenzymatic role of ecto-adenosine deaminase in lymphocytes (Q41745077) (← links)
• Retroviral vectors encoding ADA regulatory locus control region provide enhanced T-cell-specific transgene expression (Q41844097) (← links)
• Low nucleotide diversity in man (Q42066951) (← links)
• A study of Adenosine-Deaminase genetic polymorphism in rheumatoid arthritis. (Q42860264) (← links)
• Functional analysis of the human adenosine deaminase gene thymic regulatory region and its ability to generate position-independent transgene expression (Q43183220) (← links)