DOI: 10.1186/1471-2156-2-2. Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene

Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene

10.1186/1471-2156-2-2

Crossref journal-article

Springer Science and Business Media LLC

BMC Genetics (297)

Bibliography

Ramalho, J. S., Tolmachova, T., Hume, A. N., McGuigan, A., Gregory-Evans, C. Y., Huxley, C., & Seabra, M. C. (2001). Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene. BMC Genetics, 2(1).

Authors 7

José S Ramalho (first)
Tanya Tolmachova (additional)
Alistair N Hume (additional)
Amanda McGuigan (additional)
Cheryl Y Gregory-Evans (additional)
Clare Huxley (additional)
Miguel C Seabra (additional)

References 27 Referenced 41

Chavrier P, Goud B: The role of ARF and Rab GTPases in membrane transport. Curr Opin Cell Biol. 1999, 11: 466-475. 10.1016/S0955-0674(99)80067-2. (10.1016/S0955-0674(99)80067-2) / Curr Opin Cell Biol by P Chavrier (1999)
Brennwald P: Reversal of fortune. Do Rab GTPases act on the target membrane?. J Cell Biol. 2000, 149: 1-4. 10.1083/jcb.149.1.1. (10.1083/jcb.149.1.1) / J Cell Biol by P Brennwald (2000)
Pereira-Leal JB, Seabra MC: The mammalian Rab family of small GTPases: Definition of family and subfamily sequence motifs suggests a mechanism for functional specificity in the Ras super family. J Mol Biol. 2000, 301: 1077-1087. 10.1006/jmbi.2000.4010. (10.1006/jmbi.2000.4010) / J Mol Biol by JB Pereira-Leal (2000)
Lazar T, Gotte M, Gallwitz D: Vesicular transport: how many Ypt/Rab-GTPases make a eukaryotic cell?. Trends Biochem Sci. 1997, 22: 468-72. 10.1016/S0968-0004(97)01150-X. (10.1016/S0968-0004(97)01150-X) / Trends Biochem Sci by T Lazar (1997)
Nagata K-I, Satoh T, Itoh H, Kozasa T, Okano Y, Doi T, Kaziro Y, Nozawa Y: The ram : a novel low molecular weight GTP-binding protein cDNA from a rat megakaryocyte library. FEBS Lett. 1990, 275: 29-32. 10.1016/0014-5793(90)81431-M. (10.1016/0014-5793(90)81431-M) / FEBS Lett by K-I Nagata (1990)
Nagata K-I, Itoh H, Katada T, Takenaka K, Ui M, Kaziro Y, Nozawa Y: Purification, identification and characterization of two GTP-binding proteins with molecular weights of 25,000 and 21,000 in human platelet cytosol. J Biol Chem. 1989, 264: 17000-17005. (10.1016/S0021-9258(18)71450-6) / J Biol Chem by K-I Nagata (1989)
Seabra MC, Ho YK, Anant JS: Deficient geranylgeranylation of Ram/Rab27 in choroideremia. J Biol Chem. 1995, 270: 24420-24427. 10.1074/jbc.270.41.24420. (10.1074/jbc.270.41.24420) / J Biol Chem by MC Seabra (1995)
Chen D, Guo J, Miki T, Tachibana M, Gahl WA: Molecular cloning and characterization of Rab27a and Rab27b, novel human Rab proteins shared by melanocytes and platelets. Biochem Mol Med. 1997, 60: 27-37. 10.1006/bmme.1996.2559. (10.1006/bmme.1996.2559) / Biochem Mol Med by D Chen (1997)
Tolmachova T, Ramalho JS, Anant JS, Schultz RA, Huxley CM, Seabra MC: Cloning, mapping and characterization of the human RAB27A gene. Gene. 1999, 239: 109-116. 10.1016/S0378-1119(99)00371-6. (10.1016/S0378-1119(99)00371-6) / Gene by T Tolmachova (1999)
Ménasché G, Pastural E, Feldmann J, Certain S, Ersoy F, Dupuis S, Wulffraat N, Bianchi D, Fischer A, Le Deist F, de Saint Basile G: Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome. Nat Genet. 2000, 25: 173-176. 10.1038/76024. (10.1038/76024) / Nat Genet by G Ménasché (2000)
Pastural E, Barrat FJ, Dufourcq-Lagelouse R, Certain S, Sanal O, Jabado N, Seger R, Griscelli C, Fischer A, de Saint Basile G: Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene. Nat Genet. 1997, 16: 289-292. (10.1038/ng0797-289) / Nat Genet by E Pastural (1997)
Pastural E, Ersoy F, Yalman N, Wulffraat N, Grillo E, Ozkinay F, Tezcan I, Gediköglu G, Philippe N, Fischer A, de Saint Basile G: Two genes are responsible for Griscelli syndrome at the same 15q21 locus. Genomics. 2000, 63: 299-306. 10.1006/geno.1999.6081. (10.1006/geno.1999.6081) / Genomics by E Pastural (2000)
Wilson SM, Yip R, Swing DA, O'Sullivan N, Zhang Y, Novak EK, Swank RT, Russell LB, Copeland NG, Jenkins NA: A mutation in Rab27a causes the vesicle transport defects observed in ashen mice. Proc Natl Acad Sci USA. 2000, 97: 7933-7938. 10.1073/pnas.140212797. (10.1073/pnas.140212797) / Proc Natl Acad Sci USA by SM Wilson (2000)
Mercer JA, Seperack PK, Strobel MC, Copeland NG, Jenkins NA: Novel myosin heavy chain encoded by murine dilute coat colour locus. Nature. 1991, 349: 709-713. 10.1038/349709a0. (10.1038/349709a0) / Nature by JA Mercer (1991)
Stinchcombe JC, Griffiths GM: Regulated secretion from hemopoietic cells. J Cell Biol. 1999, 147: 1-6. 10.1083/jcb.147.1.1. (10.1083/jcb.147.1.1) / J Cell Biol by JC Stinchcombe (1999)
Hume AN, Collinson LM, Rapak A, Gomes AQ, Hopkins CR, Seabra MC: Rab27a regulates the peripheral distribution of melanosomes in melanocytes. J Cell Biol. 2001, / J Cell Biol by AN Hume (2001)
Stinchcombe JC, Barral DC, Mules EH, Booth S, Hume AN, Machesky LM, Seabra MC, Griffiths GM: Rab 27a is required for regulated secretion in cytotoxic T lymphocytes. J Cell Biol. 2001, / J Cell Biol by JC Stinchcombe (2001)
Yu W, Andersson B, Worley KC, Muzny DM, Ding Y, Liu W, Ricafrente JY, Wentland MA, Lennon G, Gibbs RA: Large-scale concatenation cDNA sequencing. Genome Res. 1997, 7: 353-358. (10.1101/gr.7.4.353) / Genome Res by W Yu (1997)
Warburg M, Sjo O, Tranebjaerg L, Fledelius HC: Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211. Am J Med Genet. 1991, 39: 288-293. (10.1002/ajmg.1320390309) / Am J Med Genet by M Warburg (1991)
Eichmuller S, Usener D, Dummer R, Stein A, Thiel D, Schadenforf D: Serological detection of cutaneous T-cell lymphoma-associated antigens. Proc Natl Acad Sci USA. 2001, / Proc Natl Acad Sci USA by S Eichmuller (2001)
Bennett DC, Cooper PJ, Dexter TJ, Devlin LM, Heasman J, Nester B: Cloned mouse melanocyte lines carrying the germline mutations albino and brown: complementation in culture. Development. 1989, 105: 379-385. (10.1242/dev.105.2.379) / Development by DC Bennett (1989)
Chen D, Guo J, Gahl WA: RAB GTPases expressed in human melanoma cells. Biochim Biophys Acta. 1997, 1355: 1-6. 10.1016/S0167-4889(96)00169-3. (10.1016/S0167-4889(96)00169-3) / Biochim Biophys Acta by D Chen (1997)
Pittler SJ, Baehr W: Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase -subunit gene of the rd mouse. Proc. Natl. Acad. Sci. USA. 1991, 88: 8322-8326. (10.1073/pnas.88.19.8322) / Proc. Natl. Acad. Sci. USA by SJ Pittler (1991)
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Dates

Type	When
Created	22 years, 10 months ago (Oct. 11, 2002, 2:40 p.m.)
Deposited	1 year, 4 months ago (April 25, 2024, 11:08 a.m.)
Indexed	2 months, 3 weeks ago (June 12, 2025, 10:45 a.m.)
Issued	24 years, 7 months ago (Feb. 2, 2001)
Published	24 years, 7 months ago (Feb. 2, 2001)
Published Online	24 years, 7 months ago (Feb. 2, 2001)

Funders 0

None

BibTeX

@article{Ramalho_2001, title={Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene}, volume={2}, ISSN={1471-2156}, url={http://dx.doi.org/10.1186/1471-2156-2-2}, DOI={10.1186/1471-2156-2-2}, number={1}, journal={BMC Genetics}, publisher={Springer Science and Business Media LLC}, author={Ramalho, José S and Tolmachova, Tanya and Hume, Alistair N and McGuigan, Amanda and Gregory-Evans, Cheryl Y and Huxley, Clare and Seabra, Miguel C}, year={2001}, month=feb }

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