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Items: 1 to 50 of 60

1.

Transcriptome sequencing of human breast cancer reveals aberrant intronic transcription in amplicons and dysregulation of alternative splicing with major therapeutic implications.

Forootan SS, Butler JM, Gardener D, Baird AE, Dodson A, Darby A, Kenny J, Hall N, Cossins AR, Foster CS, Gosden CM.

Int J Oncol. 2016 Jan;48(1):130-44. doi: 10.3892/ijo.2015.3222. Epub 2015 Oct 30.

PMID:
26530297
2.

siRNA knockdown of ribosomal protein gene RPL19 abrogates the aggressive phenotype of human prostate cancer.

Bee A, Brewer D, Beesley C, Dodson A, Forootan S, Dickinson T, Gerard P, Lane B, Yao S, Cooper CS, Djamgoz MB, Gosden CM, Ke Y, Foster CS.

PLoS One. 2011;6(7):e22672. doi: 10.1371/journal.pone.0022672. Epub 2011 Jul 22.

3.

WITHDRAWN: Chorion villus sampling versus amniocentesis for prenatal diagnosis.

Alfirevic Z, Gosden CM, Neilson JP.

Cochrane Database Syst Rev. 1996 Apr 22;(1):CD000055. Review.

PMID:
17636578
4.

Primer: tissue fixation and preservation for optimal molecular analysis of urologic tissues.

Foster CS, Gosden CM, Ke YQ.

Nat Clin Pract Urol. 2006 May;3(5):268-78. Review.

PMID:
16691240
5.

HER2/neu expression in cancer: the pathologist as diagnostician or prophet?

Foster CS, Gosden CM, Ke Y.

Hum Pathol. 2003 Jul;34(7):635-8. Review. No abstract available.

PMID:
12874757
6.

Chorion villus sampling versus amniocentesis for prenatal diagnosis.

Alfirevic Z, Gosden CM, Neilson JP.

Cochrane Database Syst Rev. 2000;(2):CD000055. Review. Update in: Cochrane Database Syst Rev. 1996;(1):CD000055.

PMID:
10796107
7.

Ontogeny of interstitial cells of Cajal in the human intestine.

Kenny SE, Connell G, Woodward MN, Lloyd DA, Gosden CM, Edgar DH, Vaillant C.

J Pediatr Surg. 1999 Aug;34(8):1241-7.

PMID:
10466604
8.

Embryonic abnormalities at medical termination of pregnancy with mifepristone and misoprostol during first trimester: observational study.

Blanch G, Quenby S, Ballantyne ES, Gosden CM, Neilson JP, Holland K.

BMJ. 1998 Jun 6;316(7146):1712-3.

10.

Partial hydatidiform mole and hypertension associated with a live fetus--variable presentation in two cases.

Nwosu EC, Ferriman E, McCormack MJ, Williams JH, Gosden CM.

Hum Reprod. 1995 Sep;10(9):2459-62.

PMID:
8530687
11.

How acute is the acute shortage of oocyte donors in the UK? Results of a British national survey.

Biljan MM, Taylor CT, Gosden CM, Jones SV, Malone CG, Kingsland CR.

Br J Obstet Gynaecol. 1995 Sep;102(9):746-7. No abstract available.

PMID:
7547768
12.

Identifying genes within microdissected genomic DNA: isolation of brain expressed genes from a translocation region associated with inherited mental illness.

Brookes AJ, Slorach EM, Evans KL, Thomson ML, Gosden CM, Muir WJ, Porteous DJ.

Mamm Genome. 1995 Apr;6(4):257-62.

PMID:
7613030
13.

When amniotic fluid cells do not grow.

Gosden CM.

Lancet. 1995 Jan 14;345(8942):78. No abstract available.

PMID:
7815884
14.

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.

Muir WJ, Gosden CM, Brookes AJ, Fantes J, Evans KL, Maguire SM, Stevenson B, Boyle S, Blackwood DH, St Clair DM, et al.

Cytogenet Cell Genet. 1995;70(1-2):35-40.

PMID:
7736785
15.

Parental origin of transcription from the human GNAS1 gene.

Campbell R, Gosden CM, Bonthron DT.

J Med Genet. 1994 Aug;31(8):607-14.

16.

Prenatal diagnosis of fragile X syndrome: management of the male fetus with a premutation.

Strain L, Porteous ME, Gosden CM, Ellis PM, Neilson JP, Bonthron DT.

Prenat Diagn. 1994 Jun;14(6):469-74.

PMID:
7937584
17.

Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Strain L, Gosden CM, Brock DJ, Bonthron DT.

Am J Hum Genet. 1994 Feb;54(2):236-43.

19.

Fetal growth retardation: associated malformations and chromosomal abnormalities.

Snijders RJ, Sherrod C, Gosden CM, Nicolaides KH.

Am J Obstet Gynecol. 1993 Feb;168(2):547-55.

PMID:
8438926
20.

Fetal facial defects: associated malformations and chromosomal abnormalities.

Nicolaides KH, Salvesen DR, Snijders RJ, Gosden CM.

Fetal Diagn Ther. 1993 Jan-Feb;8(1):1-9.

PMID:
8452644
21.

Ultrasonographically detectable markers of fetal chromosomal abnormalities.

Nicolaides KH, Snijders RJ, Gosden CM, Berry C, Campbell S.

Lancet. 1992 Sep 19;340(8821):704-7.

PMID:
1355807
22.

Strawberry-shaped skull in fetal trisomy 18.

Nicolaides KH, Salvesen DR, Snijders RJ, Gosden CM.

Fetal Diagn Ther. 1992;7(2):132-7.

PMID:
1503648
23.

Fetal nuchal oedema: associated malformations and chromosomal defects.

Nicolaides KH, Azar G, Snijders RJ, Gosden CM.

Fetal Diagn Ther. 1992;7(2):123-31.

PMID:
1503647
24.

First trimester prenatal diagnosis: chorion villus sampling or amniocentesis?

Neilson JP, Gosden CM.

Br J Obstet Gynaecol. 1991 Sep;98(9):849-52. No abstract available.

PMID:
1911603
25.

First-trimester fetal karyotyping: CVS or early amniocentesis?

Gosden CM.

Ultrasound Obstet Gynecol. 1991 Jul 1;1(4):233. No abstract available.

26.

Leber's hereditary optic neuropathy and Kearns-Sayre syndrome: mitochondrial DNA mutations.

Phillips CI, Gosden CM.

Surv Ophthalmol. 1991 May-Jun;35(6):463-72. Review. Erratum in: Surv Ophthalmol 1991 Sep-Oct;36(2):160.

PMID:
1755871
27.

Thyroid function in fetuses with chromosomal abnormalities.

Thorpe-Beeston JG, Nicolaides KH, Gosden CM, McGregor AM.

BMJ. 1991 Mar 16;302(6777):628. No abstract available.

28.

Choroid plexus cysts and chromosomal defects.

Thorpe-Beeston JG, Gosden CM, Nicolaides KH.

Br J Radiol. 1990 Oct;63(754):783-6.

PMID:
2242475
29.

Sexing the human fetus and identification of polyploid nuclei by DNA-DNA in situ hybridisation in interphase nuclei.

West JD, Gosden CM, Gosden JR, West KM, Davidson Z, Davidson C, Nicolaides KH.

Mol Reprod Dev. 1989;1(2):129-37.

PMID:
2629851
30.

Prenatal diagnosis of congenital diaphragmatic hernia: associated malformations and chromosomal defects.

Thorpe-Beeston JG, Gosden CM, Nicolaides KH.

Fetal Ther. 1989;4(1):21-8.

PMID:
2486022
31.

Mean red cell volume in normal, anemic, small, trisomic and triploid fetuses.

Nicolaides KH, Snijders RJ, Thorpe-Beeston JG, Van den Hof MC, Gosden CM, Bellingham AJ.

Fetal Ther. 1989;4(1):1-13.

PMID:
2486021
32.

Mosaic trisomy 7 confined to the placenta.

McKinley MJ, Kearney LU, Nicolaides KH, Rosevear SK, Bradley R, Heron O, Gosden CM.

Am J Med Genet. 1988 Nov;31(3):697-9. No abstract available.

PMID:
3228150
33.

Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture.

McKinley MJ, Kearney LU, Nicolaides KH, Gosden CM, Webb TP, Fryns JP.

Am J Med Genet. 1988 May-Jun;30(1-2):355-68.

PMID:
3177458
34.

Linkage heterogeneity and fragile X.

Clayton JF, Gosden CM, Hastie ND, Evans HJ.

Hum Genet. 1988 Apr;78(4):338-42.

PMID:
2896154
35.

Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.

Buchanan JA, Buckton KE, Gosden CM, Newton MS, Clayton JF, Christie S, Hastie N.

Hum Genet. 1987 Jun;76(2):165-72.

PMID:
3038730
36.

Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid.

Webb TP, Rodeck CH, Nicolaides KH, Gosden CM.

Prenat Diagn. 1987 Mar;7(3):203-14.

PMID:
3588539
37.

Why confine chorionic villus (placental) biopsy to the first trimester?

Nicolaides KH, Soothill PW, Rodeck CH, Warren RC, Gosden CM.

Lancet. 1986 Mar 8;1(8480):543-4. No abstract available.

PMID:
2869270
38.

Rapid karyotyping in non-lethal fetal malformations.

Nicolaides KH, Rodeck CH, Gosden CM.

Lancet. 1986 Feb 8;1(8476):283-7.

PMID:
2868161
39.

Prenatal diagnosis of bullous ichthyosiform erythroderma: detection of tonofilament clumps in fetal epidermal and amniotic fluid cells.

Eady RA, Gunner DB, Carbone LD, Bricarelli FD, Gosden CM, Rodeck CH.

J Med Genet. 1986 Feb;23(1):46-51.

40.

Fetoscopy in the assessment of unexplained fetal hydrops.

Nicolaides KH, Rodeck CH, Lange I, Watson J, Gosden CM, Miller D, Mibashan RS, Moniz C, Morgan-Capner P, Campbell S.

Br J Obstet Gynaecol. 1985 Jul;92(7):671-9.

PMID:
2410012
41.

Recombinant DNA technology in prenatal diagnosis.

Gosden JR, Gosden CM.

Oxf Rev Reprod Biol. 1985;7:73-117. Review. No abstract available.

PMID:
3001618
42.

Cholecystokinin and cystic fibrosis.

Gosden CM, Gosden JR.

Lancet. 1984 Dec 1;2(8414):1273. No abstract available.

PMID:
6150298
43.
44.

Rapid fetal sex determination in first trimester prenatal diagnosis by dot hybridisation of DNA probes.

Gosden JR, Gosden CM, Christie S, Morsman JM, Rodeck CH.

Lancet. 1984 Mar 10;1(8376):540-1. No abstract available.

PMID:
6142256
45.

The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis.

Gosden JR, Gosden CM, Christie S, Cooke HJ, Morsman JM, Rodeck CH.

Hum Genet. 1984;66(4):347-51.

PMID:
6539298
46.

A single-operator technique for first-trimester chorion biopsy.

Rodeck CH, Morsman JM, Nicolaides KH, McKenzie C, Gosden CM, Gosden JR.

Lancet. 1983 Dec 10;2(8363):1340-1. No abstract available.

PMID:
6139674
47.

Development of an improved technique for first-trimester microsampling of chorion.

Rodeck CH, Morsman JM, Gosden CM, Gosden JR.

Br J Obstet Gynaecol. 1983 Dec;90(12):1113-8.

PMID:
6652050
48.

Amniotic fluid cell types and culture.

Gosden CM.

Br Med Bull. 1983 Oct;39(4):348-54. Review. No abstract available.

PMID:
6357346
49.

Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.

Webb T, Gosden CM, Rodeck CH, Hamill MA, Eason PE.

Prenat Diagn. 1983 Apr-Jun;3(2):131-7.

PMID:
6622392
50.

Direct vision chorion biopsy and chromosome-specific DNA probes for determination of fetal sex in first-trimester prenatal diagnosis.

Gosden JR, Mitchell AR, Gosden CM, Rodeck CH, Morsman JM.

Lancet. 1982 Dec 25;2(8313):1416-9.

PMID:
6129505

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