ANKH
ANKH (ANKH inorganic pyrophosphate transport regulator) هوَ بروتين يُشَفر بواسطة جين ANKH في الإنسان.[1][2][3]
المراجع
- "Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH"، Am J Hum Genet، 71 (4): 985–91، سبتمبر 2002، doi:10.1086/343053، PMC 419998، PMID 12297989.
- "Entrez Gene: ANKH ankylosis, progressive homolog (mouse)"، مؤرشف من الأصل في 6 مارس 2010.
- "Role of the mouse ank gene in control of tissue calcification and arthritis"، Science، 289 (5477): 265–70، يوليو 2000، doi:10.1126/science.289.5477.265، PMID 10894769.
قراءة متعمقة
- Williams CJ (2003)، "Familial calcium pyrophosphate dihydrate deposition disease and the ANKH gene."، Current Opinion in Rheumatology، 15 (3): 326–31، doi:10.1097/00002281-200305000-00023، PMID 12707589.
- "The ANKH gene and familial calcium pyrophosphate dihydrate deposition disease."، Joint Bone Spine، 71 (5): 365–8، 2005، doi:10.1016/j.jbspin.2004.01.011، PMID 15474385.
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides."، Gene، 138 (1–2): 171–4، 1994، doi:10.1016/0378-1119(94)90802-8، PMID 8125298.
- "Localisation of a gene for chondrocalcinosis to chromosome 5p."، Hum. Mol. Genet.، 4 (7): 1225–8، 1996، doi:10.1093/hmg/4.7.1225، PMID 8528213.
- "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library."، Gene، 200 (1–2): 149–56، 1997، doi:10.1016/S0378-1119(97)00411-3، PMID 9373149.
- "The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene."، Am. J. Hum. Genet.، 61 (4): 918–23، 1997، doi:10.1086/514880، PMC 1716005، PMID 9382103.
- "Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease."، Am. J. Hum. Genet.، 64 (1): 136–45، 1999، doi:10.1086/302186، PMC 1377711، PMID 9915952.
- "Physical map and characterization of transcripts in the candidate interval for familial chondrocalcinosis at chromosome 5p15.1."، Genomics، 62 (2): 177–83، 2000، doi:10.1006/geno.1999.5997، PMID 10610710.
- "Prediction of the coding sequences of unidentified human genes. XVIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro."، DNA Res.، 7 (4): 273–81، 2001، doi:10.1093/dnares/7.4.271، PMID 10997877.
- "Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia."، Nat. Genet.، 28 (1): 37–41، 2001، doi:10.1038/88236، PMID 11326272.
- "Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK."، Am. J. Hum. Genet.، 68 (6): 1321–6، 2001، doi:10.1086/320612، PMC 1226118، PMID 11326338.
- "The program of androgen-responsive genes in neoplastic prostate epithelium."، Proceedings of the National Academy of Sciences of the United States of America، 99 (18): 11890–5، 2002، doi:10.1073/pnas.182376299، PMC 129364، PMID 12185249.
- "Mutations in ANKH cause chondrocalcinosis."، Am. J. Hum. Genet.، 71 (4): 933–40، 2002، doi:10.1086/343054، PMC 378546، PMID 12297987.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences."، Proceedings of the National Academy of Sciences of the United States of America، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Novel genetic markers in the 5'-flanking region of ANKH are associated with ankylosing spondylitis."، Arthritis Rheum.، 48 (3): 791–7، 2003، doi:10.1002/art.10844، PMID 12632434.
- "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment."، Genome Res.، 13 (10): 2265–70، 2003، doi:10.1101/gr.1293003، PMC 403697، PMID 12975309.
- "Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition disease."، Arthritis Rheum.، 48 (9): 2627–31، 2003، doi:10.1002/art.11133، PMID 13130483.
بوابة طب
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
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