CDC73

Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae), also known as CDC73, is a human gene. [cite web | title = Entrez Gene: CDC73 Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=79577| accessdate = ]

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References

Further reading

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*cite journal | author=Szabó J, Heath B, Hill VM, "et al." |title=Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. |journal=Am. J. Hum. Genet. |volume=56 |issue= 4 |pages= 944–50 |year= 1995 |pmid= 7717405 |doi=
*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Sood R, Bonner TI, Makalowska I, "et al." |title=Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus. |journal=Genomics |volume=73 |issue= 2 |pages= 211–22 |year= 2001 |pmid= 11318611 |doi= 10.1006/geno.2001.6500
*cite journal | author=Hobbs MR, Rosen IB, Jackson CE |title=Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2. |journal=Am. J. Hum. Genet. |volume=70 |issue= 5 |pages= 1376–7 |year= 2002 |pmid= 11951180 |doi=
*cite journal | author=Carpten JD, Robbins CM, Villablanca A, "et al." |title=HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. |journal=Nat. Genet. |volume=32 |issue= 4 |pages= 676–80 |year= 2003 |pmid= 12434154 |doi= 10.1038/ng1048
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Howell VM, Haven CJ, Kahnoski K, "et al." |title=HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. |journal=J. Med. Genet. |volume=40 |issue= 9 |pages= 657–63 |year= 2003 |pmid= 12960210 |doi=
*cite journal | author=Shattuck TM, Välimäki S, Obara T, "et al." |title=Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. |journal=N. Engl. J. Med. |volume=349 |issue= 18 |pages= 1722–9 |year= 2003 |pmid= 14585940 |doi= 10.1056/NEJMoa031237
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Simonds WF, Robbins CM, Agarwal SK, "et al." |title=Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. |journal=J. Clin. Endocrinol. Metab. |volume=89 |issue= 1 |pages= 96–102 |year= 2004 |pmid= 14715834 |doi=
*cite journal | author=Warner J, Epstein M, Sweet A, "et al." |title=Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications. |journal=J. Med. Genet. |volume=41 |issue= 3 |pages= 155–60 |year= 2004 |pmid= 14985373 |doi=
*cite journal | author=Villablanca A, Calender A, Forsberg L, "et al." |title=Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). |journal=J. Med. Genet. |volume=41 |issue= 3 |pages= e32 |year= 2004 |pmid= 14985403 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 221 |year= 2004 |pmid= 15046050 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 222 |year= 2004 |pmid= 15046094 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 222 |year= 2004 |pmid= 15046098 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 223 |year= 2004 |pmid= 15046102 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 223 |year= 2004 |pmid= 15046105 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 223 |year= 2004 |pmid= 15046107 |doi=
*cite journal | author=Teh BT, Howell VM, Haven CJ, "et al." |title=Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. |journal=Hum. Genet. |volume=114 |issue= 2 |pages= 224 |year= 2004 |pmid= 15046109 |doi=

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