PRB4

Proline-rich protein BstNI subfamily 4, also known as PRB4, is a human gene.cite web | title = Entrez Gene: PRB4 proline-rich protein BstNI subfamily 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5545| accessdate = ]

PBB_Summary
section_title =
summary_text = The protein encoded by this gene is a proline-rich salivary protein. This gene and five other genes that also encode salivary proline-rich proteins (PRPs), as well as a gene encoding a lacrimal gland PRP, form a PRP gene cluster in the chromosomal 12p13 region.cite web | title = Entrez Gene: PRB4 proline-rich protein BstNI subfamily 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5545| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Azen EA, Maeda N |title=Molecular genetics of human salivary proteins and their polymorphisms. |journal=Adv. Hum. Genet. |volume=17 |issue= |pages= 141–99 |year= 1988 |pmid= 3055850 |doi=
*cite journal | author=Bennick A |title=Salivary proline-rich proteins. |journal=Mol. Cell. Biochem. |volume=45 |issue= 2 |pages= 83–99 |year= 1982 |pmid= 6810092 |doi=
*cite journal | author=Lyons KM, Stein JH, Smithies O |title=Length polymorphisms in human proline-rich protein genes generated by intragenic unequal crossing over. |journal=Genetics |volume=120 |issue= 1 |pages= 267–78 |year= 1989 |pmid= 2851479 |doi=
*cite journal | author=Maeda N, Kim HS, Azen EA, Smithies O |title=Differential RNA splicing and post-translational cleavages in the human salivary proline-rich protein gene system. |journal=J. Biol. Chem. |volume=260 |issue= 20 |pages= 11123–30 |year= 1985 |pmid= 2993301 |doi=
*cite journal | author=Lyons KM, Azen EA, Goodman PA, Smithies O |title=Many protein products from a few loci: assignment of human salivary proline-rich proteins to specific loci. |journal=Genetics |volume=120 |issue= 1 |pages= 255–65 |year= 1989 |pmid= 3220251 |doi=
*cite journal | author=Warner TF, Azen EA |title=Proline-rich proteins are present in serous cells of submucosal glands in the respiratory tract. |journal=Am. Rev. Respir. Dis. |volume=130 |issue= 1 |pages= 115–8 |year= 1984 |pmid= 6377992 |doi=
*cite journal | author=Saitoh E, Isemura S, Sanada K |title=Complete amino acid sequence of a basic proline-rich peptide, P-D, from human parotid saliva. |journal=J. Biochem. |volume=93 |issue= 2 |pages= 495–502 |year= 1983 |pmid= 6841349 |doi=
*cite journal | author=Kauffman DL, Keller PJ, Bennick A, Blum M |title=Alignment of amino acid and DNA sequences of human proline-rich proteins. |journal=Crit. Rev. Oral Biol. Med. |volume=4 |issue= 3-4 |pages= 287–92 |year= 1993 |pmid= 8373986 |doi=
*cite journal | author=Kim HS, Lyons KM, Saitoh E, "et al." |title=The structure and evolution of the human salivary proline-rich protein gene family. |journal=Mamm. Genome |volume=4 |issue= 1 |pages= 3–14 |year= 1993 |pmid= 8422499 |doi=
*cite journal | author=Azen EA, Amberger E, Fisher S, "et al." |title=PRB1, PRB2, and PRB4 coded polymorphisms among human salivary concanavalin-A binding, II-1, and Po proline-rich proteins. |journal=Am. J. Hum. Genet. |volume=58 |issue= 1 |pages= 143–53 |year= 1996 |pmid= 8554050 |doi=
*cite journal | author=Castle AM, Castle JD |title=Enhanced glycosylation and sulfation of secretory proteoglycans is coupled to the expression of a basic secretory protein. |journal=Mol. Biol. Cell |volume=9 |issue= 3 |pages= 575–83 |year= 1998 |pmid= 9487127 |doi=
*cite journal | author=Chan M, Bennick A |title=Proteolytic processing of a human salivary proline-rich protein precursor by proprotein convertases. |journal=Eur. J. Biochem. |volume=268 |issue= 12 |pages= 3423–31 |year= 2001 |pmid= 11422372 |doi=
*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=Vallat JM, Magy L, Lagrange E, "et al." |title=Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance. |journal=Acta Neuropathol. |volume=113 |issue= 4 |pages= 443–9 |year= 2007 |pmid= 17294201 |doi= 10.1007/s00401-007-0196-7

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