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S Lindsay

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X Chromosome

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Majlinda Lako; S Lindsay; Joy Lincoln; Paul M Cairns; Lyle Armstrong; Nicholas Hole
Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.
Sally-Ann Lynch; Y Wang; Tom Strachan; John Burn; S Lindsay
Autosomal dominant sacral agenesis: Currarino syndrome.
Mark Clement-Jones; Simone Schiller; Ercole Rao; Rüdiger J Blaschke; Aimée Zuniga; Rolf Zeller; Steve C Robson; G Binder; Ian A Glass; Tom Strachan; S Lindsay; Gudrun A Rappold
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

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All Publications

2001: Majlinda Lako; S Lindsay; Joy Lincoln; Paul M Cairns; Lyle Armstrong; Nicholas Hole
Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.
Mechanisms of development 2001;103(1-2):49-59.
2000: Sally-Ann Lynch; Y Wang; Tom Strachan; John Burn; S Lindsay
Autosomal dominant sacral agenesis: Currarino syndrome.
Journal of medical genetics 2000;37(8):561-6.
2000: Mark Clement-Jones; Simone Schiller; Ercole Rao; Rüdiger J Blaschke; Aimée Zuniga; Rolf Zeller; Steve C Robson; G Binder; Ian A Glass; Tom Strachan; S Lindsay; Gudrun A Rappold
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.
Human molecular genetics 2000;9(5):695-702.
2000: Neil A Hanley; Donna-Marie Hagan; Mark Clement-Jones; SG Ball; Tom Strachan; L Salas-Cortés; Ken McElreavey; S Lindsay; Steve C Robson; PJ Bullen; Harry Ostrer; David I Wilson
SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development.
Mechanisms of development 2000;91(1-2):403-7.
2000: Françoise Fougerousse; PJ Bullen; M Herasse; S Lindsay; Isabelle Richard; D Wilson; Laurence Suel; Muriel Durand; Steve C Robson; M Abitbol; Jacques Beckmann; Tom Strachan
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.
Human molecular genetics 2000;9(2):165-73.
1999: Neil A Hanley; SG Ball; Mark Clement-Jones; Donna-Marie Hagan; Tom Strachan; S Lindsay; Steve C Robson; Harry Ostrer; Keith L Parker; David I Wilson
Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination.
Mechanisms of development 1999;87(1-2):175-80.
1999: J Rankin; Tom Strachan; Majlinda Lako; S Lindsay
Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization.
Cytogenetics and cell genetics 1999;84(1-2):50-2.
1998: Reid Huber; R Mazzarella; C N Chen; E Chen; M Ireland; S Lindsay; Giuseppe Pilia; Laura Crisponi
Glypican 3 and glypican 4 are juxtaposed in Xq26.1.
Gene 1998;225(1-2):9-16.
1998: A J Ross; Victor L Ruiz-Perez; Y Wang; Donna-Marie Hagan; S Scherer; Sally-Ann Lynch; S Lindsay; E Custard; E Belloni; David I Wilson; R Wadey; Frances R Goodman; K H Orstavik; T Monclair; Steve C Robson; William Reardon; John Burn; Peter J Scambler; Tom Strachan
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
Nature genetics 1998;20(4):358-61.
1998: Majlinda Lako; Tom Strachan; PJ Bullen; David I Wilson; Steve C Robson; S Lindsay
Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung.
Gene 1998;219(1-2):101-10.
1998: Majlinda Lako; S Lindsay; PJ Bullen; David I Wilson; Steve C Robson; Tom Strachan
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain.
Human molecular genetics 1998;7(5):813-22.
1997: S Lindsay; M Ireland; O O'Brien; Jill Clayton-Smith; Jane A Hurst; J Mann; T Cole; J Sampson; S Slaney; David Schlessinger; John Burn; Giuseppe Pilia
Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.
Journal of medical genetics 1997;34(6):480-3.
1997: Thuan Dinh Bui; Majlinda Lako; S Lejeune; Andrew R J Curtis; Tom Strachan; S Lindsay; Adrian L Harris
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25.
Gene 1997;189(1):25-9.
1996: Majlinda Lako; T Strachan; A R Curtis; S Lindsay
Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.
Genomics 1996;35(2):386-8.
1996: S Lindsay; M Splitt; S Edney; T P Berney; S J Knight; K E Davies; O O'Brien; M Gale; John Burn
PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28.
American journal of human genetics 1996;58(6):1120-6.
1995: M Ireland; C English; I Cross; S Lindsay; T Strachan
Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.
Journal of medical genetics 1995;32(10):837-8.
1995: Dawn L Thiselton; S Lindsay; S Kamakari; Alison J Hardcastle; P Roustan; Shomi S Bhattacharya
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.
Genomics 1995;25(1):279-81.
1995: S Kamakari; Dawn L Thiselton; S Lindsay; Alison J Hardcastle; Shomi Bhattacharya
FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp.
Cytogenetics and cell genetics 1995;71(2):151-4.
1994: S D Bryce; S Lindsay; A J Gladstone; K Braithwaite; C Chapman; N K Spurr; J Lunec
A novel family of cathepsin L-like (CTSLL) sequences on human chromosome 10q and related transcripts.
Genomics 1994;24(3):568-76.
1994: A R Curtis; S Lindsay; E Boye; A J Clarke; S J Landy; Shomi S Bhattacharya
A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28.
European journal of human genetics : EJHG 1994;2(1):51-8.
1993: I A Glass; P Good; M P Coleman; P Fullwood; M G Giles; S Lindsay; A H Nemeth; Kay E Davies; H A Willshaw; A Fielder
Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.
Journal of medical genetics 1993;30(12):1044-50.
1993: S Lindsay; A R Curtis; P Roustan; S Kamakari; Dawn L Thiselton; A Stephenson; Shomi S Bhattacharya
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.
Genomics 1993;17(1):208-10.
1993: Dawn L Thiselton; S Kamakari; A R Curtis; M P Coleman; Kay E Davies; S Lindsay; Shomi Bhattacharya
Dinucleotide repeat polymorphism at the DXS556 locus.
Human molecular genetics 1993;2(5):613.
1993: P Roustan; A R Curtis; S Kamakari; Dawn L Thiselton; S Lindsay; Shomi S Bhattacharya
Dinucleotide repeat polymorphism at the DXS573 locus.
Human molecular genetics 1993;2(1):92.
1993: A R Curtis; S Headland; S Lindsay; N S Thomas; E Boye; S Kamakari; P Roustan; M Anvret; J Wahlstrom; G McCarthy
X chromosome linkage studies in familial Rett syndrome.
Human genetics 1993;90(5):551-5.
1992: P Roustan; A R Curtis; S Kamakari; Dawn L Thiselton; S Lindsay; Shomi S Bhattacharya
Dinucleotide repeat polymorphism at the DXS559 locus.
Human molecular genetics 1992;1(9):778.
1992: A R Curtis; P Roustan; S Kamakari; Dawn L Thiselton; S Lindsay; Shomi S Bhattacharya
Two dinucleotide repeat polymorphisms at the DXS571 locus.
Human molecular genetics 1992;1(9):776.
1992: M E M Porteous; A Curtis; S Lindsay; O Williams; D Goudie; S Kamakari; Shomi S Bhattacharya
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).
Genomics 1992;14(2):298-301.
1992: S Lindsay; Chris F Inglehearn; A Curtis; Shomi Bhattacharya
Molecular genetics of inherited retinal degenerations.
Current opinion in genetics & development 1992;2(3):459-66.
1992: S Lindsay; Dawn L Thiselton; J B Bateman; J T Ngo; RS Sparkes; M Coleman; Kay E Davies; Shomi S Bhattacharya
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.
Human genetics 1992;88(3):349-50.
1991: M P Coleman; J C Murray; H F Willard; K F Nolan; K B Reid; Derek J Blake; S Lindsay; S S Bhattacharya; A Wright; Kay E Davies
Genetic and physical mapping around the properdin P gene.
Genomics 1991;11(4):991-6.
1990: M Coleman; S Bhattacharya; S Lindsay; A Wright; M Jay; M Litt; I Craig; K Davies
Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.
American journal of human genetics 1990;47(6):935-40.
1989: S Lindsay; MR Jay; D J Bower; G Adam; Chris F Inglehearn; P G Sealey; Surinder S Papiha; Shomi S Bhattacharya
X-linked retinitis pigmentosa: a molecular genetic approach to isolating the defective genes.
Progress in clinical and biological research 1989;314():83-97.