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Items: 40

1.

Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.

Floros VI, Pyle A, Dietmann S, Wei W, Tang WWC, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, Surani MA, Chinnery PF.

Nat Cell Biol. 2018 Aug;20(8):991. doi: 10.1038/s41556-018-0064-9.

PMID:
29674682
2.

Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.

Floros VI, Pyle A, Dietmann S, Wei W, Tang WCW, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, Surani MA, Chinnery PF.

Nat Cell Biol. 2018 Feb;20(2):144-151. doi: 10.1038/s41556-017-0017-8. Epub 2018 Jan 15. Erratum in: Nat Cell Biol. 2018 Apr 19;:.

3.

The formation of endoderm-derived taste sensory organs requires a Pax9-dependent expansion of embryonic taste bud progenitor cells.

Kist R, Watson M, Crosier M, Robinson M, Fuchs J, Reichelt J, Peters H.

PLoS Genet. 2014 Oct 9;10(10):e1004709. doi: 10.1371/journal.pgen.1004709. eCollection 2014 Oct.

4.

Abnormal retinal development associated with FRMD7 mutations.

Thomas MG, Crosier M, Lindsay S, Kumar A, Araki M, Leroy BP, McLean RJ, Sheth V, Maconachie G, Thomas S, Moore AT, Gottlob I.

Hum Mol Genet. 2014 Aug 1;23(15):4086-93. doi: 10.1093/hmg/ddu122. Epub 2014 Mar 31.

5.

The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain.

Ehrmann I, Dalgliesh C, Liu Y, Danilenko M, Crosier M, Overman L, Arthur HM, Lindsay S, Clowry GJ, Venables JP, Fort P, Elliott DJ.

PLoS Genet. 2013 Apr;9(4):e1003474. doi: 10.1371/journal.pgen.1003474. Epub 2013 Apr 25.

6.

Origin of trisomy: no evidence to support the ovarian mosaicism theory.

Morris CR, Haigh S, Cuthbert G, Crosier M, Harding F, Wolstenholme J.

Prenat Diagn. 2012 Jul;32(7):668-73. doi: 10.1002/pd.3885. Epub 2012 May 9.

PMID:
22570272
7.

Improving satisfaction in patients receiving mental health care: a case study.

Crosier M, Scott J, Steinfeld B.

J Behav Health Serv Res. 2012 Jan;39(1):42-54. doi: 10.1007/s11414-011-9252-0.

PMID:
21847711
8.

Matrix Gla protein polymorphism, but not concentrations, is associated with radiographic hand osteoarthritis.

Misra D, Booth SL, Crosier MD, Ordovas JM, Felson DT, Neogi T.

J Rheumatol. 2011 Sep;38(9):1960-5. doi: 10.3899/jrheum.100985. Epub 2011 Jul 1.

9.

Circulating uncarboxylated matrix gla protein is associated with vitamin K nutritional status, but not coronary artery calcium, in older adults.

Shea MK, O'Donnell CJ, Vermeer C, Magdeleyns EJ, Crosier MD, Gundberg CM, Ordovas JM, Kritchevsky SB, Booth SL.

J Nutr. 2011 Aug;141(8):1529-34. doi: 10.3945/jn.111.139634. Epub 2011 May 31.

10.

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.

Bakircioglu M, Carvalho OP, Khurshid M, Cox JJ, Tuysuz B, Barak T, Yilmaz S, Caglayan O, Dincer A, Nicholas AK, Quarrell O, Springell K, Karbani G, Malik S, Gannon C, Sheridan E, Crosier M, Lisgo SN, Lindsay S, Bilguvar K, Gergely F, Gunel M, Woods CG.

Am J Hum Genet. 2011 May 13;88(5):523-35. doi: 10.1016/j.ajhg.2011.03.019. Epub 2011 Apr 28.

11.

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

Thomas MG, Crosier M, Lindsay S, Kumar A, Thomas S, Araki M, Talbot CJ, McLean RJ, Surendran M, Taylor K, Leroy BP, Moore AT, Hunter DG, Hertle RW, Tarpey P, Langmann A, Lindner S, Brandner M, Gottlob I.

Brain. 2011 Mar;134(Pt 3):892-902. doi: 10.1093/brain/awq373. Epub 2011 Feb 8.

12.

Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy.

Polster B, Crosier M, Lindsay S, Hayflick S.

Brain Res Bull. 2010 Nov 20;83(6):374-9. doi: 10.1016/j.brainresbull.2010.08.011. Epub 2010 Sep 9.

13.

Associations of APOE gene polymorphisms with bone mineral density and fracture risk: a meta-analysis.

Peter I, Crosier MD, Yoshida M, Booth SL, Cupples LA, Dawson-Hughes B, Karasik D, Kiel DP, Ordovas JM, Trikalinos TA.

Osteoporos Int. 2011 Apr;22(4):1199-209. doi: 10.1007/s00198-010-1311-5. Epub 2010 Jun 9. Review.

14.

A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly.

Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA.

Am J Hum Genet. 2009 Dec;85(6):897-902. doi: 10.1016/j.ajhg.2009.10.027.

15.

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development.

Betts-Henderson J, Bartesaghi S, Crosier M, Lindsay S, Chen HL, Salomoni P, Gottlob I, Nicotera P.

Hum Mol Genet. 2010 Jan 15;19(2):342-51. doi: 10.1093/hmg/ddp500. Epub 2009 Nov 5.

PMID:
19892780
16.

Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome.

Vega H, Trainer AH, Gordillo M, Crosier M, Kayserili H, Skovby F, Uzielli ML, Schnur RE, Manouvrier S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Hennekam RC, Jabs EW.

J Med Genet. 2010 Jan;47(1):30-7. doi: 10.1136/jmg.2009.068395. Epub 2009 Jul 1.

PMID:
19574259
17.

Association of sequence variations in vitamin K epoxide reductase and gamma-glutamyl carboxylase genes with biochemical measures of vitamin K status.

Crosier MD, Peter I, Booth SL, Bennett G, Dawson-Hughes B, Ordovas JM.

J Nutr Sci Vitaminol (Tokyo). 2009 Apr;55(2):112-9.

18.

Matrix Gla protein polymorphisms are associated with coronary artery calcification in men.

Crosier MD, Booth SL, Peter I, Dawson-Hughes B, Price PA, O'Donnell CJ, Hoffmann U, Williamson MK, Ordovas JM.

J Nutr Sci Vitaminol (Tokyo). 2009 Feb;55(1):59-65.

19.

Are comparisons of consumer satisfaction with providers biased by nonresponse or case-mix differences?

Simon G, Rutter C, Crosier M, Scott J, Operskalski BH, Ludman E.

Psychiatr Serv. 2009 Jan;60(1):67-73. doi: 10.1176/appi.ps.60.1.67.

20.

Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome.

Miyake N, Chilton J, Psatha M, Cheng L, Andrews C, Chan WM, Law K, Crosier M, Lindsay S, Cheung M, Allen J, Gutowski NJ, Ellard S, Young E, Iannaccone A, Appukuttan B, Stout JT, Christiansen S, Ciccarelli ML, Baldi A, Campioni M, Zenteno JC, Davenport D, Mariani LE, Sahin M, Guthrie S, Engle EC.

Science. 2008 Aug 8;321(5890):839-43. doi: 10.1126/science.1156121. Epub 2008 Jul 24.

21.

Personality assessment in today's health care environment: therapeutic alliance and patient satisfaction.

Quirk MP, Erdberg P, Crosier M, Steinfeld B.

J Pers Assess. 2007 Oct;89(2):95-104. Review.

PMID:
17764387
22.
23.

DNA sequence and analysis of human chromosome 9.

Humphray SJ, Oliver K, Hunt AR, Plumb RW, Loveland JE, Howe KL, Andrews TD, Searle S, Hunt SE, Scott CE, Jones MC, Ainscough R, Almeida JP, Ambrose KD, Ashwell RI, Babbage AK, Babbage S, Bagguley CL, Bailey J, Banerjee R, Barker DJ, Barlow KF, Bates K, Beasley H, Beasley O, Bird CP, Bray-Allen S, Brown AJ, Brown JY, Burford D, Burrill W, Burton J, Carder C, Carter NP, Chapman JC, Chen Y, Clarke G, Clark SY, Clee CM, Clegg S, Collier RE, Corby N, Crosier M, Cummings AT, Davies J, Dhami P, Dunn M, Dutta I, Dyer LW, Earthrowl ME, Faulkner L, Fleming CJ, Frankish A, Frankland JA, French L, Fricker DG, Garner P, Garnett J, Ghori J, Gilbert JG, Glison C, Grafham DV, Gribble S, Griffiths C, Griffiths-Jones S, Grocock R, Guy J, Hall RE, Hammond S, Harley JL, Harrison ES, Hart EA, Heath PD, Henderson CD, Hopkins BL, Howard PJ, Howden PJ, Huckle E, Johnson C, Johnson D, Joy AA, Kay M, Keenan S, Kershaw JK, Kimberley AM, King A, Knights A, Laird GK, Langford C, Lawlor S, Leongamornlert DA, Leversha M, Lloyd C, Lloyd DM, Lovell J, Martin S, Mashreghi-Mohammadi M, Matthews L, McLaren S, McLay KE, McMurray A, Milne S, Nickerson T, Nisbett J, Nordsiek G, Pearce AV, Peck AI, Porter KM, Pandian R, Pelan S, Phillimore B, Povey S, Ramsey Y, Rand V, Scharfe M, Sehra HK, Shownkeen R, Sims SK, Skuce CD, Smith M, Steward CA, Swarbreck D, Sycamore N, Tester J, Thorpe A, Tracey A, Tromans A, Thomas DW, Wall M, Wallis JM, West AP, Whitehead SL, Willey DL, Williams SA, Wilming L, Wray PW, Young L, Ashurst JL, Coulson A, Blöcker H, Durbin R, Sulston JE, Hubbard T, Jackson MJ, Bentley DR, Beck S, Rogers J, Dunham I.

Nature. 2004 May 27;429(6990):369-74.

24.

Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p.

Guy J, Hearn T, Crosier M, Mudge J, Viggiano L, Koczan D, Thiesen HJ, Bailey JA, Horvath JE, Eichler EE, Earthrowl ME, Deloukas P, French L, Rogers J, Bentley D, Jackson MS.

Genome Res. 2003 Feb;13(2):159-72.

25.

Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.

Crosier M, Viggiano L, Guy J, Misceo D, Stones R, Wei W, Hearn T, Ventura M, Archidiacono N, Rocchi M, Jackson MS.

Genome Res. 2002 Jan;12(1):67-80.

26.

High expression of the trefoil protein TFF1 in interval breast cancers.

Crosier M, Scott D, Wilson RG, Griffiths CD, May FE, Westley BR.

Am J Pathol. 2001 Jul;159(1):215-21.

27.

Radiographic diagnosis: fracture of the caudal aspect of the greater tubercle of the humerus in a horse.

Tudor R, Crosier M, Bowman KF.

Vet Radiol Ultrasound. 2001 May-Jun;42(3):244-5. No abstract available.

PMID:
11405267
28.

Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10q.

Guy J, Spalluto C, McMurray A, Hearn T, Crosier M, Viggiano L, Miolla V, Archidiacono N, Rocchi M, Scott C, Lee PA, Sulston J, Rogers J, Bentley D, Jackson MS.

Hum Mol Genet. 2000 Aug 12;9(13):2029-42.

PMID:
10942432
29.

A look to the past, directions for the future.

Quirk MP, Simon G, Todd J, Horst T, Crosier M, Ekorenrud B, Goepfert R, Baker N, Steinfeld B, Rosenberg M, Strosahl K.

Psychiatr Q. 2000 Spring;71(1):79-95.

PMID:
10736818
30.

Differences in Ki67 and c-erbB2 expression between screen-detected and true interval breast cancers.

Crosier M, Scott D, Wilson RG, Griffiths CD, May FE, Westley BR.

Clin Cancer Res. 1999 Oct;5(10):2682-8.

31.

Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locations.

Jackson MS, Rocchi M, Thompson G, Hearn T, Crosier M, Guy J, Kirk D, Mulligan L, Ricco A, Piccininni S, Marzella R, Viggiano L, Archidiacono N.

Hum Mol Genet. 1999 Feb;8(2):205-15.

PMID:
9931328
32.

Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110).

Armour JA, Crosier M, Jeffreys AJ.

Ann Hum Genet. 1996 Jan;60(1):11-20.

PMID:
8835094
33.

Human minisatellite loci composed of interspersed GGA-GGT triplet repeats.

Armour JA, Crosier M, Malcolm S, Chan JC, Jeffreys AJ.

Proc Biol Sci. 1995 Sep 22;261(1362):345-9.

PMID:
8587876
34.

Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA.

Royle NJ, Armour JA, Crosier M, Jeffreys AJ.

Genomics. 1993 Jan;15(1):119-22.

PMID:
8432522
35.
36.

Human minisatellite alleles detectable only after PCR amplification.

Armour JA, Crosier M, Jeffreys AJ.

Genomics. 1992 Jan;12(1):116-24.

PMID:
1733848
37.

A highly polymorphic minisatellite (pMS627) on chromosome 14 (D14S44).

Crosier M, Armour JA, Jeffreys AJ.

Nucleic Acids Res. 1991 Oct 11;19(19):5446. No abstract available.

38.

A polymorphic minisatellite (pMS628) on chromosome 3 (D3S1084).

Armour JA, Crosier M, Jeffreys AJ.

Nucleic Acids Res. 1991 Oct 11;19(19):5447. No abstract available.

39.

A highly polymorphic minisatellite (pMS626) on chromosome 13 (D13S103).

Armour JA, Crosier M, Jeffreys AJ.

Nucleic Acids Res. 1991 Oct 11;19(19):5447. No abstract available.

40.

Principles and recent advances in human DNA fingerprinting.

Jeffreys AJ, Royle NJ, Patel I, Armour JA, MacLeod A, Collick A, Gray IC, Neumann R, Gibbs M, Crosier M, et al.

EXS. 1991;58:1-19. Review.

PMID:
1831152

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