UCL School of Life and Medical Sciences

2013

• Sebire NJ, Miller S, Jacques TS, Taylor AM, Rennie JM, Kendall G, Chitty LS (2013). Post-mortem apparent resolution of fetal ventriculomegaly: Evidence from magnetic resonance imaging. Prenatal Diagnosis, 33(4), 360 - 364.
• Dlamini N, Josifova DJ, Paine SML, Wraige E, Pitt M, Murphy AJ, King A, Buk S, Smith F, Abbs S, Sewry C, Jacques TS, Jungbluth H (2013). Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene. Neuromuscular Disorders, 23(5), 391 - 398.
• Barba C, Jacques T, Kahane P, Polster T, Isnard J, Leijten FSS, Ozkara C, Tassi L, Giordano F, Castagna M, John A, Öz B, Salon C, Streichenberger N, Cross JH, Guerrini R (2013). Epilepsy surgery in Neurofibromatosis Type 1. Epilepsy Research, , - .
• Thurston B, Gunny R, Anderson G, Paine S, Thompson D, Jacques T, Ternier J (2013). Fourth ventricle rosette-forming glioneuronal tumour in children: An unusual presentation in an 8-year-old patient, discussion and review of the literature. Child's Nervous System, 29(5), 839 - 847.
• Thurston B, Gunny R, Anderson G, Paine S, Thompson D, Jacques T, Ternier J (2013). Fourth ventricle rosette-forming glioneuronal tumour in children: an unusual presentation in an 8-year-old patient, discussion and review of the literature.. Childs Nerv Syst, 29(5), 839 - 847. doi:10.1007/s00381-012-1993-4
• Jethwa H, Jacques TS, Gunny R, Wedderburn LR, Pilkington C, Manzur AY (2013). Limb girdle muscular dystrophy type 2B masquerading as inflammatory myopathy: case report.. Pediatr Rheumatol Online J, 11(1), 19 - . doi:10.1186/1546-0096-11-19
• McTague A, Appleton R, Avula S, Cross JH, King MD, Jacques TS, Bhate S, Cronin A, Curran A, Desurkar A, Farrell MA, Hughes E, Jefferson R, Lascelles K, Livingston J, Meyer E, McLellan A, Poduri A, Scheffer IE, Spinty S, Kurian MA, Kneen R (2013). Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum.. Brain, 136(Pt 5), 1578 - 1591. doi:10.1093/brain/awt073
• Shepherd C, Liu J, Goc J, Martinian L, Jacques TS, Sisodiya SM, Thom M (2013). A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II.. Epilepsia, 54(5), 898 - 908. doi:10.1111/epi.12143
• Dlamini N, Josifova DJ, Paine SML, Wraige E, Pitt M, Murphy AJ, King A, Buk S, Smith F, Abbs S, others (2013). Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the< i> UBA1 gene. Neuromuscular Disorders, , - .
• Shepherd C, Liu J, Goc J, Martinian L, Jacques TS, Sisodiya SM, Thom M (2013). A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II. Epilepsia, 54(5), 898 - 908.
• Sebire NJ, Miller S, Jacques TS, Taylor AM, Rennie JM, Kendall G, Chitty LS (2013). Post-mortem apparent resolution of fetal ventriculomegaly: evidence from magnetic resonance imaging.. Prenat Diagn, 33(4), 360 - 364. doi:10.1002/pd.4065

2012

• D'Argenzio L, Colonnelli MC, Harrison S, Jacques TS, Harkness W, Scott RC, Cross JH (2012). Seizure outcome after extratemporal epilepsy surgery in childhood. Developmental Medicine and Child Neurology, 54(11), 995 - 1000.
• Tirabosco R, Jacques T, Berisha F, Flanagan AM (2012). Assessment of integrase interactor 1 (INI-1) expression in primary tumours of bone. Histopathology, , - .
• Coras R, De Boer OJ, Armstrong D, Becker A, Jacques TS, Miyata H, Thom M, Vinters HV, Spreafico R, Oz B, Marucci G, Pimentel J, Mühlebner A, Zamecnik J, Buccoliero AM, Rogerio F, Streichenberger N, Arai N, Bugiani M, Vogelgesang S, MacAulay R, Salon C, Hans V, Polivka M, Giangaspero F, Fauziah D, Kim J-H, Liu L, Dandan W, Gao J, Lindeboom B, Blümcke I, Aronica E (2012). Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias. Epilepsia, 53(8), 1341 - 1348.
• Tirabosco R, Jacques T, Berisha F, Flanagan AM (2012). Assessment of integrase interactor 1 (INI-1) expression in primary tumours of bone. Histopathology, 61(6), 1245 - 1247.
• Scoto M, Cullup T, Cirak S, Yau M, Feng L, Manzur A, Jungbluth H, Abbs S, Sewry C, Muntoni F (2012). Nebulin mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing. NEUROMUSCULAR DISORDERS, 22, S31 - S31.
• Apps J, Hasan F, Campus O, Behjati S, Jacques T, Sebire N, J A (2012). The immune environment of paediatric solid malignancies; evidence from an immunohistochemical study of clinical cases. Fetal and Pediatric Pathology, In press, - .
• Munot P, Saunders DE, Milewicz DM, Regalado ES, Ostergaard JR, Braun KP, Kerr T, Lichtenbelt KD, Philip S, Rittey C, Jacques TS, Cox TC, Ganesan V (2012). A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations.. Brain, 135(Pt 8), 2506 - 2514. doi:10.1093/brain/aws172
• Andoniadou CL, Gaston-Massuet C, Reddy R, Schneider RP, Blasco MA, Le Tissier P, Jacques TS, Pevny LH, Dattani MT, Martinez-Barbera JP (2012). Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma. Acta Neuropathologica, , 1 - 13.
• Winder-Rhodes SE, Garcia-Reitböck P, Ban M, Evans JR, Jacques TS, Kemppinen A, Foltynie T, Williams-Gray CH, Chinnery PF, Hudson G, Burn DJ, Allcock LM, Sawcer SJ, Barker RA, Spillantini MG (2012). Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome. Movement Disorders, 27(2), 312 - 315.
• Kinsler VA, Paine SML, Anderson GW, Wijesekara DS, Sebire NJ, Chong WK, Harkness W, Aylett SE, Jacques TS (2012). Neuropathology of neurocutaneous melanosis: Histological foci of melanotic neurones and glia may be undetectable on MRI. Acta Neuropathologica, 123(3), 453 - 456.
• Coras R, de Boer OJ, Armstrong D, Becker A, Jacques TS, Miyata H, Thom M, Vinters HV, Spreafico R, Oz B, Marucci G, Pimentel J, Mühlebner A, Zamecnik J, Buccoliero AM, Rogerio F, Streichenberger N, Arai N, Bugiani M, Vogelgesang S, Macaulay R, Salon C, Hans V, Polivka M, Giangaspero F, Fauziah D, Kim JH, Liu L, Dandan W, Gao J, Lindeboom B, Blümcke I, Aronica E (2012). Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias.. Epilepsia, 53(8), 1341 - 1348. doi:10.1111/j.1528-1167.2012.03508.x
• D'Argenzio L, Colonnelli MC, Harrison S, Jacques TS, Harkness W, Scott RC, Cross JH (2012). Seizure outcome after extratemporal epilepsy surgery in childhood.. Dev Med Child Neurol, 54(11), 995 - 1000. doi:10.1111/j.1469-8749.2012.04381.x
• Andoniadou CL, Gaston-Massuet C, Reddy R, Schneider RP, Blasco MA, Le Tissier P, Jacques TS, Pevny LH, Dattani MT, Martinez-Barbera JP (2012). Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngioma.. Acta Neuropathol, 124(2), 259 - 271. doi:10.1007/s00401-012-0957-9
• Pryce JW, Paine SML, Weber MA, Harding B, Jacques TS, Sebire NJ (2012). Role of routine neuropathological examination for determining cause of death in sudden unexpected deaths in infancy (SUDI). Journal of Clinical Pathology, 65(3), 257 - 261.
• Paine SML, Munot P, Carmichael J, Das K, Weber MA, Prabhakar P, Jacques TS (2012). The neuropathological consequences of CDKL5 mutation. Neuropathology and applied neurobiology, 38, 744 - 747.
• Paine SML, Grünewald S, Jacques TS (2012). Antenatal neurodevelopmental defects in ornithine transcarbamylase deficiency. Neuropathology and Applied Neurobiology, 38(5), 509 - 512. doi:10.1111/j.1365-2990.2012.01262.x

2011

• Gaston-Massuet C, Andoniadou CL, Signore M, Jayakody SA, Charolidi N, Kyeyune R, Vernay B, Jacques TS, Taketo MM, Le Tissier P, Dattani MT, Martinez-Barbera JP (2011). Increased Wingless (Wnt) signaling in pituitary progenitor/stem cells gives rise to pituitary tumors in mice and humans.. Proc Natl Acad Sci U S A, 108(28), 11482 - 11487. doi:10.1073/pnas.1101553108
• Presneau N, Shalaby A, Ye H, Pillay N, Halai D, Idowu B, Tirabosco R, Whitwell D, Jacques TS, Kindblom LG, Brüderlein S, Möller P, Leithner A, Liegl B, Amary FM, Athanasou NN, Hogendoorn PC, Mertens F, Szuhai K, Flanagan AM (2011). Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.. J Pathol, 223(3), 327 - 335. doi:10.1002/path.2816
• Kelberman D, Islam L, Jacques TS, Russell-Eggitt I, Bitner-Glindzicz M, Khaw PT, Nischal KK, Sowden JC (2011). CYP1B1-related anterior segment developmental anomalies: Novel mutations for infantile glaucoma and von Hippel's ulcer revisited. Ophthalmology, 118(9), 1865 - 1873.
• JACQUES T, Harkness W (2011). Ganglioglioma, dysembryoplastic neuroepithelial tumours, and related tumours. In Shorvon SD, Andermann F, Guerrini R (Ed.), The Causes of Epilepsy (pp. - ). : Cambridge Univ Pr.
• Kelberman D, Islam L, Jacques TS, Russell-Eggitt I, Bitner-Glindzicz M, Khaw PT, Nischal KK, Sowden JC (2011). CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.. Ophthlamology, 118(9), 1865 - 1873.
• Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM (2011). Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.. Brain, 134(Pt 10), 2982 - 3010. doi:10.1093/brain/awr129
• Kelberman D, Islam L, Holder SE, Jacques TS, Calvas P, Hennekam RC, Nischal KK, Sowden JC (2011). Digenic Inheritance of Mutations in FOXC1 and PITX2: Correlating Transcription Factor Function and Axenfeld-Rieger Disease Severity. HUM MUTAT, 32(10), 1144 - 1152. doi:10.1002/humu.21550
• Menghi F, Jacques TS, Barenco M, Schwalbe EC, Clifford SC, Hubank M, Ham J (2011). Genome-wide analysis of alternative splicing in medulloblastoma identifies splicing patterns characteristic of normal cerebellar development. Cancer Res., 71(6), 2045 - 2055. doi:10.1158/0008-5472.CAN-10-2519
• Blümcke I, Thom M, Aronica E, Armstrong DD, Vinters HV, Palmini A, Jacques TS, Avanzini G, Barkovich AJ, Battaglia G, Becker A, Cepeda C, Cendes F, Colombo N, Crino P, Cross JH, Delalande O, Dubeau F, Duncan J, Guerrini R, Kahane P, Mathern G, Najm I, Ozkara C, Raybaud C, Represa A, Roper SN, Salamon N, Schulze-Bonhage A, Tassi L, Vezzani A, Spreafico R (2011). The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission(1). Epilepsia, 52(1), 158 - 174. doi:10.1111/j.1528-1167.2010.02777.x
• D'Argenzio L, Colonnelli MC, Harrison S, Jacques TS, Harkness W, Vargha-Khadem F, Scott RC, Cross JH (2011). Cognitive outcome after extratemporal epilepsy surgery in childhood.. Epilepsia, 52(11), 1966 - 1972. doi:10.1111/j.1528-1167.2011.03272.x

2010

• Bossley C, Hogg C, Stoneham S, Jacques TS, Bush A (2010). A fatal case of cough. Pediatric Pulmonology, 45(2), 205 - 207.
• Jacques TS, Sebire NJ (2010). The impact of article titles on citation hits: an analysis of general and specialist medical journals. J R Soc Med Sh Rep, 1, 2 - . doi:10.1258/shorts.2009.100020
• Jacques TS, Swales A, Brzozowski MJ, Henriquez NV, Linehan JM, Mirzadeh Z, O' Malley C, Naumann H, Alvarez-Buylla A, Brandner S (2010). Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes.. EMBO J, 29(1), 222 - 235. doi:10.1038/emboj.2009.327
• Presneau N, Shalaby A, Ye H, Pillay N, Halai D, Idowu B, Tirabosco R, Whitwell D, Jacques TS, Kindblom LG, Brüderlein S, Möller P, Leithner A, Liegl B, Amary FM, Athanasou NN, Hogendoorn PC, Mertens F, Szuhai K, Flanagan AM (2010). Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.. J Pathol, , - . doi:10.1002/path.2816
• Lawson ARJ, Tatevossian RG, Phipps KP, Picker SR, Michalski A, Sheer D, Jacques TS, Forshew T (2010). RAF gene fusions are specific to pilocytic astrocytoma in a broad paediatric brain tumour cohort. ACTA NEUROPATHOL, 120(2), 271 - 273. doi:10.1007/s00401-010-0693-y
• Yasin SA, Latak K, Becherini F, Ganapathi A, Miller K, Campos O, Picker SR, Bier N, Smith M, Thom M, Anderson G, Cross JH, Harkness W, Harding B, Jacques TS (2010). Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell. Acta Neuropathologica, , - . doi:10.1007/s00401-010-0677-y
• Kristiansen M, Hughes R, Patel P, Jacques TS, Clark AR, Ham J (2010). Mkp1 is a c-Jun target gene that antagonizes JNK-dependent apoptosis in sympathetic neurons. Journal of Neuroscience, 30(32), 10820 - 10832. doi:10.1523/​JNEUROSCI.2824-10.2010

2009

• Sebire N, Malone M, Ashworth M, Jacques TS (2009). Diagnostic pediatric surgical pathology.
• Trotz M, Weber MA, Jacques TS, Malone M, Sebire NJ (2009). Disseminated langerhans cell histiocytosis-related sudden unexpected death in infancy. Fetal and Pediatric Pathology, 28(1), 39 - 44.
• Cohen NR, Phipps K, Harding B, Jacques TS (2009). Is CSF cytology a useful diagnostic procedure in staging paediatric CNS tumours?. Cytopathology, 20(4), 256 - 260.
• Potter NE, Phipps K, Harkness W H, R TD, Jacques TS, Harding B, Thomas DGT, Rees J, Darling JL, Warr TJ (2009). Astrocytoma derived short-term cell cultures retain molecular signatures characteristic of the tumour in situ. Experimental Cell Research, 315(16), 2835 - 2846. doi:10.1016/j.yexcr.2009.06.003
• Thayyil S, Robertson NJ, Scales A, Weber MA, Jacques TS, Sebire NJ, Taylor AMMMRIASCG (2009). Prospective parental consent for autopsy research following sudden unexpected childhood deaths: a successful model. Archives of Disease in Childhood, 94(5), 354 - 358. doi:10.1136/adc.2008.150904
• Stacpoole SRL, Phadke R, Jacques TS, Revesz T, Plant GT (2009). Vacuolar myelopathy associated with optic neuropathy in an HIV-negative, immunosuppressed liver transplant recipient. Journal of Neurology, Neurosurgery and Psychiatry, 80(5), 581 - 583. doi:10.1136/jnnp.2008.150292

2008

• Jacques T, Harding B (2008). New developments in “shaken baby syndrome”. Advances in Clinical Neuroscience and Rehabilitation, 8, 24 - 25.
• Apostolidis A, Jacques TS, Freeman A, Kalsi V, Popat R, Gonzales G, Datta SN, Ghazi-Noori S, Elneil S, Dasgupta P, Fowler CJ (2008). Histological changes in the urothelium and suburothelium of human overactive bladder following intradetrusor injections of botulinum neurotoxin type A for the treatment of neurogenic or idiopathic detrusor overactivity. European Urology, 53(6), 1245 - 1253. doi:10.1016/j.eururo.2008.02.037
• Karakoula K, Suarez-Merino B, Ward S, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Beck J, Thomas DGT, Warr TJ (2008). Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13. Genes, Chromosomes and Cancer, 47(11), 1005 - 1022. doi:10.1002/gcc.20607
• Jacques TS, Miller K, Rampling D, Gatscher S, Harding B (2008). Peritoneal dissemination of a malignant glioma. Cytopathology, , - .
• Potter N, Karakoula A, Phipps KP, Harkness W, Hayward R, Thompson DN, Jacques TS, Harding B, Thomas DG, Palmer RW, Rees J, Darling J, Warr TJ (2008). Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma. Neoplasia, 10(8), 757 - 772. doi:10.1593/neo.07914
• Hassan HM, McAndrew PT, Yagan A, Jacques TS, Hayward R (2008). Mature orbital teratoma presenting as a recurrent orbital cellulitis with an ectopic tooth and sphenoid malformation-a case report. Orbit, 27(4), 309 - 12. doi:10.1080/01676830802222902

2007

• Tofaris GK, Revesz T, Jacques TS, Papacostas S, Chataway J (2007). Adult-onset neurodegeneration with brain iron accumulation and cortical alpha-synuclein and tau pathology: a distinct clinicopathological entity. Archives of Neurology, 64(2), 280 - 282. doi:10.1001/archneur.64.2.280

2006

• Jacques TS, Galloway MJ, Scaravilli F (2006). Cerebrospinal fluid findings in central neurocytoma. Cytopathology, 17(5), 301 - 303. doi:10.1111/j.1365-2303.2006.00296.x
• Trivedi SG, Newson J, Rajakariar R, Jacques TS, Hannon R, Kanaoka Y, Eguchi N, Colville-Nash P, Gilroy DW (2006). Essential role for hematopoietic prostaglandin D2 synthase in the control of delayed type hypersensitivity. Proceedings Of The National Academy Of Sciences Of The United States Of America, 103(13), 5179 - 5184. doi:10.1073/pnas.0507175103
• Vujovic S, Henderson S, Presneau N, Odell E, Jacques TS, Tirabosco R, Boshoff C, Flanagan AM (2006). Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas. The Journal of pathology, 209, 157 - 165.
• Jacques TS, Eldridge C, Patel A, Saleem NM, Powell M, Kitchen ND, Thom M, Revesz T (2006). Mixed glioneuronal tumour of the fourth ventricle with prominent rosette formation.. Neuropathology and Applied Neurobiology, 32(2), 217 - 220.

2005

• Nandi M, Miller A, Stidwill R, Jacques TS, Lam AJA, Haworth S, Heales S, Vallance P (2005). Pulmonary hypertension in a GTP-cyclohydrolase 1 deficient mouse. Circulation, 111(16), 2086 - 2090. doi:10.1161/01.CIR.0000163268.32638.F4
• Pramstaller PP, Schlossmacher MG, Jacques TS, Scaravilli F, Eskelson C, Pepivani I, Hedrich K, Adel S, Gonzales-McNeal M, Hilker R, Kramer PL, Klein C (2005). Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers. ANN NEUROL, 58(3), 411 - 422. doi:10.1002/ana.20587
• Clarke AJ, Jacques TS, Galloway MJ, Thom M, Kitchen ND, Plant GT (2005). ALK positive inflammatory myofibroblastic tumour of the pineal region. Journal of Clinical Pathology, 58(9), 981 - 983.

2004

• Apostolidis AN, Yiangou Y, Brady CM, Ford AP, Baecker PA, Jacques TS, Freeman A, Fowler CJ, Anand P (2004). Endothelial nitric oxide synthase expression in neurogenic urinary bladders treated with intravesical resiniferatoxin. BJU International, 93(3), 336 - 340.
• Brady CM, Apostolidis AN, Harper M, Yiangou Y, Beckett A, Jacques TS, Freeman A, Scaravilli F, Fowler CJ, Anand P (2004). Parallel changes in bladder suburothelial vanilloid receptor TRPV1 and pan-neuronal marker PGP9.5 immunoreactivity in patients with neurogenic detrusor overactivity after intravesical resiniferatoxin treatment. BJU International, 93(6), 770 - 776.
• Brady CM, Apostolidis A, Yiangou Y, Baecker PA, Ford AP, Freeman A, Jacques TS, Fowler CJ, Anand P (2004). P2X3-immunoreactive nerve fibres in neurogenic detrusor overactivity and the effect of intravesical resiniferatoxin. European Urology, 46(2), 247 - 253.
• Jacques TS, Valentine A, Bradford R, McLaughlin JE (2004). December 2003: A 70-year-old woman with a recurrent meningeal mass. BRAIN PATHOL, 14(2), 229 - +.

2003

• Brealey DA, Karyampudi S, Jaques TS, Novelli M, Stidwill R, Taylor V, Smolenski RT, Singer M (2003). Mitochondrial dysfunction in a long-term rodent model of sepsis and organ failure. American Journal of Physiology - Regulatory, Integrative and Comparative Physiology, , - .

2002

• Jacques TS, Holton J, Watts PM, Wills AJ, Smith SE, Hanna MG (2002). Tubular aggregate myopathy with abnormal pupils and skeletal deformities. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 73(3), 324 - 326.
• Heelan B, Jacques TS, Karim MY, Bunn C (2002). Audit of IgG subclasses in adults and guidelines for their measurement. Allergy and Immunology CPD Bulletin, 2, 52 - 54.

1999

• Jacques TS, Skepper JN, Navaratnam V (1999). Fibroblast growth factor-1 improves survival and regeneration of rat vagal preganglionic neurones following axonal injury. Neuroscience Letters, 276, 197 - 200.
• Ponassi M, Jacques TS, Ciani L, ffrench Constant C (1999). Expression of the rat homologue of the Drosophila fat tumour suppressor gene.. Mech Dev, 80(2), 207 - 212.

1998

• Navaratnam V, Jacques TS, Skepper JN (1998). Ultrastructural and cytochemical study of neurones in the rat dorsal motor nucleus of the vagus after axon crush. Microscopy Research and Techniques, 42, 334 - 344.
• Jacques TS, Relvas J, Nishimura S, Pytela R, Edwards G, Streuli G, ffrench-Constant C (1998). Neural precursor cell chain migration and division are regulated through different β1 integrins. Development, 126, 3167 - 3177.

1997

• Jefferson S, Jacques TS, Kiernan BW, Scott-Drew S, Milner R, ffrench-Constant C (1997). Inhibition of oligodendrocyte precursor mobility by oligodendrocyte processes: implications for transplantation based approaches to multiple sclerosis. Multiple Sclerosis, 3, 162 - 167.

• Ward SJ, Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, Harding B, Darling JL, Thomas DG, Warr TJ (). Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation. Journal of Neuro-oncology, , - .