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Items: 1 to 50 of 52

1.

Widespread dynamic and pleiotropic expression of the melanocortin-1-receptor (MC1R) system is conserved across chick, mouse and human embryonic development.

Thomas AC, Heux P, Santos C, Arulvasan W, Solanky N, Carey ME, Gerrelli D, Kinsler VA, Etchevers HC.

Birth Defects Res. 2018 Mar 15;110(5):443-455. doi: 10.1002/bdr2.1183. Epub 2018 Jan 8.

PMID:
29316344
2.

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders.

Holt R, Ceroni F, Bax DA, Broadgate S, Diaz DG, Santos C, Gerrelli D, Ragge NK.

Sci Rep. 2017 Aug 11;7(1):7975. doi: 10.1038/s41598-017-08397-w.

3.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.

Evrony GD, Cordero DR, Shen J, Partlow JN, Yu TW, Rodin RE, Hill RS, Coulter ME, Lam AN, Jayaraman D, Gerrelli D, Diaz DG, Santos C, Morrison V, Galli A, Tschulena U, Wiemann S, Martel MJ, Spooner B, Ryu SC, Elhosary PC, Richardson JM, Tierney D, Robinson CA, Chibbar R, Diudea D, Folkerth R, Wiebe S, Barkovich AJ, Mochida GH, Irvine J, Lemire EG, Blakley P, Walsh CA.

Genome Res. 2017 Aug;27(8):1323-1335. doi: 10.1101/gr.219899.116. Epub 2017 Jun 19.

4.

A genomic atlas of human adrenal and gonad development.

Del Valle I, Buonocore F, Duncan AJ, Lin L, Barenco M, Parnaik R, Shah S, Hubank M, Gerrelli D, Achermann JC.

Wellcome Open Res. 2017 Apr 7;2:25. doi: 10.12688/wellcomeopenres.11253.2.

5.

Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders.

Holt R, Ugur Iseri SA, Wyatt AW, Bax DA, Gold Diaz D, Santos C, Broadgate S, Dunn R, Bruty J, Wallis Y, McMullan D, Ogilvie C, Gerrelli D, Zhang Y, Ragge N.

Hum Genet. 2017 Jan;136(1):119-127. doi: 10.1007/s00439-016-1745-8. Epub 2016 Nov 14.

PMID:
27844144
6.

Mutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment Dysgenesis.

Cheong SS, Hentschel L, Davidson AE, Gerrelli D, Davie R, Rizzo R, Pontikos N, Plagnol V, Moore AT, Sowden JC, Michaelides M, Snead M, Tuft SJ, Hardcastle AJ.

Am J Hum Genet. 2016 Dec 1;99(6):1338-1352. doi: 10.1016/j.ajhg.2016.09.022. Epub 2016 Nov 10.

7.

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development.

Lindsay SJ, Xu Y, Lisgo SN, Harkin LF, Copp AJ, Gerrelli D, Clowry GJ, Talbot A, Keogh MJ, Coxhead J, Santibanez-Koref M, Chinnery PF.

Front Neuroanat. 2016 Oct 26;10:86. eCollection 2016. No abstract available.

8.

Distinct expression patterns for type II topoisomerases IIA and IIB in the early foetal human telencephalon.

Harkin LF, Gerrelli D, Gold Diaz DC, Santos C, Alzu'bi A, Austin CA, Clowry GJ.

J Anat. 2016 Mar;228(3):452-63. doi: 10.1111/joa.12416. Epub 2015 Nov 27.

9.

Enabling research with human embryonic and fetal tissue resources.

Gerrelli D, Lisgo S, Copp AJ, Lindsay S.

Development. 2015 Sep 15;142(18):3073-6. doi: 10.1242/dev.122820.

10.

Analysis of LIN28A in early human ovary development and as a candidate gene for primary ovarian insufficiency.

El-Khairi R, Parnaik R, Duncan AJ, Lin L, Gerrelli D, Dattani MT, Conway GS, Achermann JC.

Mol Cell Endocrinol. 2012 Apr 4;351(2):264-8. doi: 10.1016/j.mce.2011.12.016. Epub 2012 Jan 3.

11.

Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth Cohort.

Hysi PG, Simpson CL, Fok YK, Gerrelli D, Webster AR, Bhattacharya SS, Hammond CJ, Sham PC, Rahi JS.

Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):440-7. doi: 10.1167/iovs.10-5640.

PMID:
22110064
12.

Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.

McCabe MJ, Gaston-Massuet C, Tziaferi V, Gregory LC, Alatzoglou KS, Signore M, Puelles E, Gerrelli D, Farooqi IS, Raza J, Walker J, Kavanaugh SI, Tsai PS, Pitteloud N, Martinez-Barbera JP, Dattani MT.

J Clin Endocrinol Metab. 2011 Oct;96(10):E1709-18. doi: 10.1210/jc.2011-0454. Epub 2011 Aug 10.

13.

Human RSPO1/R-spondin1 is expressed during early ovary development and augments β-catenin signaling.

Tomaselli S, Megiorni F, Lin L, Mazzilli MC, Gerrelli D, Majore S, Grammatico P, Achermann JC.

PLoS One. 2011 Jan 28;6(1):e16366. doi: 10.1371/journal.pone.0016366.

14.

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.

Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP.

J Med Genet. 2011 Jan;48(1):48-54. doi: 10.1136/jmg.2010.079426. Epub 2010 Oct 23.

15.

Comparison of Iroquois gene expression in limbs/fins of vertebrate embryos.

McDonald LA, Gerrelli D, Fok Y, Hurst LD, Tickle C.

J Anat. 2010 Jun;216(6):683-91. doi: 10.1111/j.1469-7580.2010.01233.x. Epub 2010 Apr 14.

16.

Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators.

Gestri G, Osborne RJ, Wyatt AW, Gerrelli D, Gribble S, Stewart H, Fryer A, Bunyan DJ, Prescott K, Collin JR, Fitzgerald T, Robinson D, Carter NP, Wilson SW, Ragge NK.

Hum Genet. 2009 Dec;126(6):791-803. doi: 10.1007/s00439-009-0730-x.

17.

Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.

Twigg SR, Versnel SL, Nürnberg G, Lees MM, Bhat M, Hammond P, Hennekam RC, Hoogeboom AJ, Hurst JA, Johnson D, Robinson AA, Scambler PJ, Gerrelli D, Nürnberg P, Mathijssen IM, Wilkie AO.

Am J Hum Genet. 2009 May;84(5):698-705. doi: 10.1016/j.ajhg.2009.04.009. Epub 2009 Apr 30.

18.

Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism.

Sajedi E, Gaston-Massuet C, Signore M, Andoniadou CL, Kelberman D, Castro S, Etchevers HC, Gerrelli D, Dattani MT, Martinez-Barbera JP.

Dis Model Mech. 2008 Nov-Dec;1(4-5):241-54. doi: 10.1242/dmm.000711. Epub 2008 Nov 6.

19.

CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease.

Ferraz-de-Souza B, Martin F, Mallet D, Hudson-Davies RE, Cogram P, Lin L, Gerrelli D, Beuschlein F, Morel Y, Huebner A, Achermann JC.

J Clin Endocrinol Metab. 2009 Feb;94(2):678-83. doi: 10.1210/jc.2008-1064. Epub 2008 Nov 4.

20.

Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.

Rajab A, Kelberman D, de Castro SC, Biebermann H, Shaikh H, Pearce K, Hall CM, Shaikh G, Gerrelli D, Grueters A, Krude H, Dattani MT.

Hum Mol Genet. 2008 Jul 15;17(14):2150-9. doi: 10.1093/hmg/ddn114. Epub 2008 Apr 10.

PMID:
18407919
21.

Neuronal function of Tbx20 conserved from nematodes to vertebrates.

Pocock R, Mione M, Hussain S, Maxwell S, Pontecorvi M, Aslam S, Gerrelli D, Sowden JC, Woollard A.

Dev Biol. 2008 May 15;317(2):671-85. doi: 10.1016/j.ydbio.2008.02.015. Epub 2008 Feb 21.

22.

SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development.

Kelberman D, de Castro SC, Huang S, Crolla JA, Palmer R, Gregory JW, Taylor D, Cavallo L, Faienza MF, Fischetto R, Achermann JC, Martinez-Barbera JP, Rizzoti K, Lovell-Badge R, Robinson IC, Gerrelli D, Dattani MT.

J Clin Endocrinol Metab. 2008 May;93(5):1865-73. doi: 10.1210/jc.2007-2337. Epub 2008 Feb 19.

23.

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.

Bakrania P, Efthymiou M, Klein JC, Salt A, Bunyan DJ, Wyatt A, Ponting CP, Martin A, Williams S, Lindley V, Gilmore J, Restori M, Robson AG, Neveu MM, Holder GE, Collin JR, Robinson DO, Farndon P, Johansen-Berg H, Gerrelli D, Ragge NK.

Am J Hum Genet. 2008 Feb;82(2):304-19. doi: 10.1016/j.ajhg.2007.09.023. Epub 2008 Jan 31.

24.

Transient expression of the conserved zinc finger gene INSM1 in progenitors and nascent neurons throughout embryonic and adult neurogenesis.

Duggan A, Madathany T, de Castro SC, Gerrelli D, Guddati K, García-Añoveros J.

J Comp Neurol. 2008 Apr 1;507(4):1497-520. doi: 10.1002/cne.21629.

PMID:
18205207
25.

Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation.

Sisodiya SM, Thompson PJ, Need A, Harris SE, Weale ME, Wilkie SE, Michaelides M, Free SL, Walley N, Gumbs C, Gerrelli D, Ruddle P, Whalley LJ, Starr JM, Hunt DM, Goldstein DB, Deary IJ, Moore AT.

J Med Genet. 2007 Jun;44(6):373-80. Epub 2007 Jan 19.

26.

Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure.

Ybot-Gonzalez P, Savery D, Gerrelli D, Signore M, Mitchell CE, Faux CH, Greene ND, Copp AJ.

Development. 2007 Feb;134(4):789-99. Epub 2007 Jan 17.

27.

The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.

Dawe HR, Smith UM, Cullinane AR, Gerrelli D, Cox P, Badano JL, Blair-Reid S, Sriram N, Katsanis N, Attie-Bitach T, Afford SC, Copp AJ, Kelly DA, Gull K, Johnson CA.

Hum Mol Genet. 2007 Jan 15;16(2):173-86. Epub 2006 Dec 21.

PMID:
17185389
28.

Heterozygous mutations of OTX2 cause severe ocular malformations.

Ragge NK, Brown AG, Poloschek CM, Lorenz B, Henderson RA, Clarke MP, Russell-Eggitt I, Fielder A, Gerrelli D, Martinez-Barbera JP, Ruddle P, Hurst J, Collin JR, Salt A, Cooper ST, Thompson PJ, Sisodiya SM, Williamson KA, Fitzpatrick DR, van Heyningen V, Hanson IM.

Am J Hum Genet. 2005 Jun;76(6):1008-22. Epub 2005 Apr 21. Erratum in: Am J Hum Genet. 2005 Aug;77(2):334.

29.

Cordon-bleu is a conserved gene involved in neural tube formation.

Carroll EA, Gerrelli D, Gasca S, Berg E, Beier DR, Copp AJ, Klingensmith J.

Dev Biol. 2003 Oct 1;262(1):16-31.

30.

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ.

Brain. 2003 Nov;126(Pt 11):2455-62. Epub 2003 Jul 22.

PMID:
12876151
31.

Genomic organization and embryonic expression of Igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia.

Murdoch JN, Doudney K, Gerrelli D, Wortham N, Paternotte C, Stanier P, Copp AJ.

Mol Cell Neurosci. 2003 Jan;22(1):62-74.

PMID:
12595239
32.

Sonic hedgehog and the molecular regulation of mouse neural tube closure.

Ybot-Gonzalez P, Cogram P, Gerrelli D, Copp AJ.

Development. 2002 May;129(10):2507-17.

33.

Cardiovascular defects associated with abnormalities in midline development in the Loop-tail mouse mutant.

Henderson DJ, Conway SJ, Greene ND, Gerrelli D, Murdoch JN, Anderson RH, Copp AJ.

Circ Res. 2001 Jul 6;89(1):6-12.

34.

Neurulation and neural tube closure defects.

Copp A, Cogram P, Fleming A, Gerrelli D, Henderson D, Hynes A, Kolatsi-Joannou M, Murdoch J, Ybot-Gonzalez P.

Methods Mol Biol. 2000;136:135-60. Review. No abstract available.

PMID:
10840706
35.
36.

Failure of neural tube closure in the loop-tail (Lp) mutant mouse: analysis of the embryonic mechanism.

Gerrelli D, Copp AJ.

Brain Res Dev Brain Res. 1997 Sep 20;102(2):217-24.

PMID:
9352104
37.

Mechanisms of normal and abnormal neurulation: evidence from embryo culture studies.

Fleming A, Gerrelli D, Greene ND, Copp AJ.

Int J Dev Biol. 1997 Apr;41(2):199-212. Review.

39.

The cardiac form of the tissue-specific SmN protein is identical to the brain and embryonic forms of the protein.

Gerrelli D, Grimaldi K, Horn D, Mahadeva U, Sharpe N, Latchman DS.

J Mol Cell Cardiol. 1993 Mar;25(3):321-9.

PMID:
8510173
40.
41.

Cloning and sequencing of a mouse embryonal carcinoma cell mRNA encoding the tissue specific RNA splicing protein SmN.

Gerrelli D, Sharpe NG, Latchman DS.

Nucleic Acids Res. 1991 Dec 11;19(23):6642. No abstract available.

42.

The relationship between appetite and plasma non-esterified fatty acid levels in housed calves.

Fox MT, Gerrelli D, Pitt SR, Jacobs DE.

Vet Res Commun. 1991;15(2):127-33.

PMID:
2068796
43.

Ostertagia ostertagi infection in the calf: effects of a trickle challenge on the hormonal control of digestive and metabolic function.

Fox MT, Gerrelli D, Pitt SR, Jacobs DE, Gill M, Simmonds AD.

Res Vet Sci. 1989 Nov;47(3):299-304.

PMID:
2595087
44.
45.

Influence of an OPRB on immunity to gastrointestinal nematodes: a field study.

Jacobs DE, Fox MT, Pilkington JG, Gerrelli D.

Vet Rec. 1989 May 13;124(19):510. No abstract available.

PMID:
2756621
46.

Effect of omeprazole treatment on feed intake and blood gastrin and pepsinogen levels in the calf.

Fox MT, Gerrelli D, Shivalkar P, Jacobs DE.

Res Vet Sci. 1989 Mar;46(2):280-2.

PMID:
2704894
47.

Blood gastrin and pepsinogen responses to subclinical infection with Ostertagia ostertagi in adult dairy cattle.

Pitt SR, Fox MT, Gerrelli D, Jacobs DE.

Res Vet Sci. 1988 Jul;45(1):130-1.

PMID:
3222546
48.

Effect of diet on gastrin response to Ostertagia ostertagi infection in the calf.

Fox MT, Pitt SR, Gerrelli D, Jacobs DE.

Int J Parasitol. 1988 Jun;18(4):547-8. No abstract available.

PMID:
3417383
49.

Endocrine effects of a trickle infection with Dictyocaulus viviparus in the calf.

Fox MT, Pitt SR, Gerrelli D, Jacobs DE, Simmonds AD.

Int J Parasitol. 1988 Jun;18(4):549-51. No abstract available.

PMID:
2971022
50.

Use of blood gastrin assay in the diagnosis of ovine haemonchiasis.

Fox MT, Pitt SR, Gerrelli D, Jacobs DE, Adhikari DR, Goddard PJ.

Vet Rec. 1988 Feb 6;122(6):136-7. No abstract available.

PMID:
3369065

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