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Items: 1 to 50 of 63

1.

Obituary: Mary F Lyon (1925–2014).

Rastan S.

Reprod Biomed Online. 2015 Jun;30(6):566-7. No abstract available.

PMID:
26247070
2.

Mary F. Lyon (1925-2014).

Rastan S.

Nature. 2015 Feb 5;518(7537):36. doi: 10.1038/518036a. No abstract available.

PMID:
25652989
3.

Measuring chemical emissions from wet products--development of a new measurement technique.

Wang R, Zhu J, Rastan S, Haghighat F.

J Hazard Mater. 2011 Sep 15;192(3):1026-32. doi: 10.1016/j.jhazmat.2011.06.004. Epub 2011 Jun 12.

PMID:
21723663
4.

Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.

Tsipouri V, Curtin JA, Nolan PM, Vizor L, Parsons CA, Clapham CM, Latham ID, Rooke LJ, Martin JE, Peters J, Hunter AJ, Rogers D, Rastan S, Brown SD, Fisher EM, Spurr NK, Gray IC.

Comp Funct Genomics. 2004;5(2):123-7. doi: 10.1002/cfg.382.

5.

Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2.

Hough TA, Polewski M, Johnson K, Cheeseman M, Nolan PM, Vizor L, Rastan S, Boyde A, Pritzker K, Hunter AJ, Fisher EM, Terkeltaub R, Brown SD.

J Bone Miner Res. 2007 Sep;22(9):1397-407.

6.

Applied K fertilizer use efficiency in pineapples grown on a tropical peat soil under residues removal.

Ahmed OH, Ahmad HM, Musa HM, Rahim AA, Rastan SO.

ScientificWorldJournal. 2005 Jan 21;5:42-9.

7.

Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders.

Rastan S, Hough T, Kierman A, Hardisty R, Erven A, Gray IC, Voeling S, Isaacs A, Tsai H, Strivens M, Washbourne R, Thornton C, Greenaway S, Hewitt M, McCormick S, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Mburu P, Rogers D, Hagan J, Reavill C, Davies K, Glenister P, Fisher EM, Martin J, Vizor L, Bouzyk M, Kelsell D, Guenet JL, Steel KP, Sheardown S, Spurr N, Gray I, Peters J, Nolan PM, Hunter AJ, Brown SD.

Genetica. 2004 Sep;122(1):47-9.

PMID:
15619960
8.

Manipulation of the mouse genome: a multiple impact resource for drug discovery and development.

Prosser H, Rastan S.

Trends Biotechnol. 2003 May;21(5):224-32. Review.

PMID:
12727384
9.

Novel phenotypes identified by plasma biochemical screening in the mouse.

Hough TA, Nolan PM, Tsipouri V, Toye AA, Gray IC, Goldsworthy M, Moir L, Cox RD, Clements S, Glenister PH, Wood J, Selley RL, Strivens MA, Vizor L, McCormack SL, Peters J, Fisher EM, Spurr N, Rastan S, Martin JE, Brown SD, Hunter AJ.

Mamm Genome. 2002 Oct;13(10):595-602.

PMID:
12420138
10.

Genetic analysis of the mouse brain proteome.

Klose J, Nock C, Herrmann M, Stühler K, Marcus K, Blüggel M, Krause E, Schalkwyk LC, Rastan S, Brown SD, Büssow K, Himmelbauer H, Lehrach H.

Nat Genet. 2002 Apr;30(4):385-93. Epub 2002 Mar 25.

PMID:
11912495
11.

Identification and characterization of alternatively spliced murine Rgs11 isoforms: genomic structure and gene analysis.

Giudice A, Gould JA, Freeman KB, Rastan S, Hertzog P, Kola I, Iannello RC.

Cytogenet Cell Genet. 2001;94(3-4):216-24.

PMID:
11856884
12.

Obituary. Rosa Beddington (1956-2001).

Rastan S, Robertson E.

Nature. 2001 Jul 12;412(6843):138. No abstract available.

PMID:
11449257
13.

Genomics: saviour or millstone?

Rastan S.

Trends Genet. 2001 May;17(5):247-8.

PMID:
11426417
14.

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

Tsai H, Hardisty RE, Rhodes C, Kiernan AE, Roby P, Tymowska-Lalanne Z, Mburu P, Rastan S, Hunter AJ, Brown SD, Steel KP.

Hum Mol Genet. 2001 Mar 1;10(5):507-12.

PMID:
11181574
15.

Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean.

Clapham JC, Arch JR, Chapman H, Haynes A, Lister C, Moore GB, Piercy V, Carter SA, Lehner I, Smith SA, Beeley LJ, Godden RJ, Herrity N, Skehel M, Changani KK, Hockings PD, Reid DG, Squires SM, Hatcher J, Trail B, Latcham J, Rastan S, Harper AJ, Cadenas S, Buckingham JA, Brand MD, Abuin A.

Nature. 2000 Jul 27;406(6794):415-8.

PMID:
10935638
16.

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson JA, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel KP, Voegeling S, Guenet JL, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher EM, Martin J, Rastan S, Brown SD, Hunter J.

Nat Genet. 2000 Aug;25(4):440-3.

PMID:
10932191
17.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.

Isaacs AM, Davies KE, Hunter AJ, Nolan PM, Vizor L, Peters J, Gale DG, Kelsell DP, Latham ID, Chase JM, Fisher EM, Bouzyk MM, Potter A, Masih M, Walsh FS, Sims MA, Doncaster KE, Parsons CA, Martin J, Brown SD, Rastan S, Spurr NK, Gray IC.

Hum Mol Genet. 2000 Jul 22;9(12):1865-71.

PMID:
10915775
18.

Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.

Nolan PM, Peters J, Vizor L, Strivens M, Washbourne R, Hough T, Wells C, Glenister P, Thornton C, Martin J, Fisher E, Rogers D, Hagan J, Reavill C, Gray I, Wood J, Spurr N, Browne M, Rastan S, Hunter J, Brown SD.

Mamm Genome. 2000 Jul;11(7):500-6.

PMID:
10886012
19.

The Pro-115 --> Gln mutation in peroxisome-proliferator-activated receptor (PPAR) gamma2 is extremely rare in a large cohort of U.S. Caucasians.

Terrett J, Chamberlain J, Rastan S, Marshall R, McGinnis R, Spurr N, O'Brien E, Evans C, Rut A.

Clin Sci (Lond). 2000 Jul;99(1):89-90. No abstract available.

PMID:
10887062
20.

Neuropilin-2 is required in vivo for selective axon guidance responses to secreted semaphorins.

Giger RJ, Cloutier JF, Sahay A, Prinjha RK, Levengood DV, Moore SE, Pickering S, Simmons D, Rastan S, Walsh FS, Kolodkin AL, Ginty DD, Geppert M.

Neuron. 2000 Jan;25(1):29-41.

21.

Functional genomics: going forwards from the databases.

Rastan S, Beeley LJ.

Curr Opin Genet Dev. 1997 Dec;7(6):777-83. Review.

PMID:
9468787
22.

Regulatory elements in the minimal promoter region of the mouse Xist gene.

Sheardown SA, Newall AE, Norris DP, Rastan S, Brockdorff N.

Gene. 1997 Dec 12;203(2):159-68.

PMID:
9426246
23.

Stabilization of Xist RNA mediates initiation of X chromosome inactivation.

Sheardown SA, Duthie SM, Johnston CM, Newall AE, Formstone EJ, Arkell RM, Nesterova TB, Alghisi GC, Rastan S, Brockdorff N.

Cell. 1997 Oct 3;91(1):99-107.

24.

Of men in mice.

Rastan S.

Nat Genet. 1997 Jun;16(2):113-4. No abstract available.

PMID:
9171817
25.

NIEHS/EPA Workshops. Genomic imprinting.

Stewart CL, Pedersen R, Rotwein P, Bestor T, Rastan S, Hastie N, Nichols R, Mutter G.

Reprod Toxicol. 1997 Mar-Jun;11(2-3):309-16. No abstract available.

PMID:
9100305
26.

A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2.

Collignon J, Sockanathan S, Hacker A, Cohen-Tannoudji M, Norris D, Rastan S, Stevanovic M, Goodfellow PN, Lovell-Badge R.

Development. 1996 Feb;122(2):509-20.

27.

Requirement for Xist in X chromosome inactivation.

Penny GD, Kay GF, Sheardown SA, Rastan S, Brockdorff N.

Nature. 1996 Jan 11;379(6561):131-7.

PMID:
8538762
28.

Cloning and characterization of a new human Xq13 gene, encoding a putative helicase.

Stayton CL, Dabovic B, Gulisano M, Gecz J, Broccoli V, Giovanazzi S, Bossolasco M, Monaco L, Rastan S, Boncinelli E, et al.

Hum Mol Genet. 1994 Nov;3(11):1957-64.

PMID:
7874112
29.

Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development.

Kay GF, Barton SC, Surani MA, Rastan S.

Cell. 1994 Jun 3;77(5):639-50.

PMID:
8205614
30.

Evidence that random and imprinted Xist expression is controlled by preemptive methylation.

Norris DP, Patel D, Kay GF, Penny GD, Brockdorff N, Sheardown SA, Rastan S.

Cell. 1994 Apr 8;77(1):41-51.

PMID:
8156596
31.

X chromosome inactivation and the Xist gene.

Rastan S.

Curr Opin Genet Dev. 1994 Apr;4(2):292-7. Review.

PMID:
8032207
32.

Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal.

Capel B, Rasberry C, Dyson J, Bishop CE, Simpson E, Vivian N, Lovell-Badge R, Rastan S, Cattanach BM.

Nat Genet. 1993 Nov;5(3):301-7.

PMID:
8275095
33.

YAC clone contigs surrounding the Zfx and Pola loci on the mouse X chromosome.

Hamvas RM, Larin Z, Brockdorff N, Rastan S, Lehrach H, Chartier FL, Brown SD.

Genomics. 1993 Jul;17(1):52-8.

PMID:
8406471
34.

Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus.

Cooper P, Keer JT, McCabe VM, Hamvas RM, Brown SD, Rastan S, Brockdorff N.

Genomics. 1993 Mar;15(3):570-5.

PMID:
8468051
35.

Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation.

Kay GF, Penny GD, Patel D, Ashworth A, Brockdorff N, Rastan S.

Cell. 1993 Jan 29;72(2):171-82.

PMID:
8425217
36.

Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.

Zonana J, Gault J, Davies KJ, Jones M, Browne D, Litt M, Brockdorff N, Rastan S, Clarke A, Thomas NS.

Am J Hum Genet. 1993 Jan;52(1):78-84.

37.

Encyclopedia of the mouse genome III. October 1993. Mouse X chromosome.

Brown SD, Avner P, Boyd Y, Chapman V, Rastan S, Sefton L, Thomas JD, Herman GE.

Mamm Genome. 1993;4 Spec No:S269-81. No abstract available.

PMID:
8268681
38.

High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Zonana J, Jones M, Browne D, Litt M, Kramer P, Becker HW, Brockdorff N, Rastan S, Davies KP, Clarke A, et al.

Am J Hum Genet. 1992 Nov;51(5):1036-46.

39.

The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus.

Brockdorff N, Ashworth A, Kay GF, McCabe VM, Norris DP, Cooper PJ, Swift S, Rastan S.

Cell. 1992 Oct 30;71(3):515-26.

PMID:
1423610
40.

Lymphoid development in mice congenitally lacking T cell receptor alpha beta-expressing cells.

Philpott KL, Viney JL, Kay G, Rastan S, Gardiner EM, Chae S, Hayday AC, Owen MJ.

Science. 1992 Jun 5;256(5062):1448-52.

PMID:
1604321
41.

A candidate spermatogenesis gene on the mouse Y chromosome is homologous to ubiquitin-activating enzyme E1.

Kay GF, Ashworth A, Penny GD, Dunlop M, Swift S, Brockdorff N, Rastan S.

Nature. 1991 Dec 12;354(6353):486-9.

PMID:
1749428
42.
43.

X-chromosome inactivation may explain the difference in viability of XO humans and mice.

Ashworth A, Rastan S, Lovell-Badge R, Kay G.

Nature. 1991 May 30;351(6325):406-8.

PMID:
2034290
44.

Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome.

Brockdorff N, Ashworth A, Kay GF, Cooper P, Smith S, McCabe VM, Norris DP, Penny GD, Patel D, Rastan S.

Nature. 1991 May 23;351(6324):329-31.

PMID:
2034279
45.

High-density molecular map of the central span of the mouse X chromosome.

Brockdorff N, Kay G, Smith S, Keer JT, Hamvas RM, Brown SD, Rastan S.

Genomics. 1991 May;10(1):17-22.

PMID:
1675191
46.

Methylation status of CpG-rich islands on active and inactive mouse X chromosomes.

Norris DP, Brockdorff N, Rastan S.

Mamm Genome. 1991;1(2):78-83.

PMID:
1799791
47.

Molecular genetic analysis of the Ta25H deletion: evidence for additional deleted loci.

Brockdorff N, Kay G, Cattanach BM, Rastan S.

Mamm Genome. 1991;1(3):152-7.

PMID:
1797229
48.

The search for the mouse X-chromosome inactivation centre.

Rastan S, Brown SD.

Genet Res. 1990 Oct-Dec;56(2-3):99-106. Review.

PMID:
2272521
49.

Construction and analysis of linking libraries from the mouse X chromosome.

Brockdorff N, Montague M, Smith S, Rastan S.

Genomics. 1990 Aug;7(4):573-8.

PMID:
2167288
50.

Czech mouse.

Rastan S.

Trends Genet. 1990 Aug;6(8):233-6. Review. No abstract available.

PMID:
1978426

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