المؤلفون: Lana-Elola, E, Cater, H, Watson-Scales, S, Greenaway, S, Müller-Winkler, J, Gibbins, D, Nemes, M, Slender, A, Hough, T, Keskivali-Bond, P, Scudamore, CL, Herbert, E, Banks, GT, Mobbs, H, Canonica, T, Tosh, J, Noy, S, Llorian, M, Nolan, PM, Griffin, JL, Good, M, Simon, M, Mallon, A-M, Wells, S, Fisher, EMC, Tybulewicz, VLJ

المصدر: Disease Models & Mechanisms (2021) (In press).

مصطلحات موضوعية: Craniofacial development, Diabetes, Down syndrome, Haematopoiesis, Hearing, Memory, Mouse model, Sleep

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10135671/1/dmm049157.pdf; https://discovery.ucl.ac.uk/id/eprint/10135671/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10135671/1/dmm049157.pdf
https://discovery.ucl.ac.uk/id/eprint/10135671/

المؤلفون: Kalisch-Smith, JI, Ved, N, Szumska, D, Munro, J, Troup, M, Harris, SE, Rodriguez-Caro, H, Jacquemot, A, Miller, JJ, Stuart, EM, Wolna, M, Hardman, E, Prin, F, Lana-Elola, E, Aoidi, R, Fisher, EMC, Tybulewicz, VLJ, Mohun, TJ, Lakhal-Littleton, S, De Val, S, Giannoulatou, E, Sparrow, DB

المصدر: Nature Communications , 12 , Article 3447. (2021)

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10129770/1/s41467-021-23660-5.pdf; https://discovery.ucl.ac.uk/id/eprint/10129770/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10129770/1/s41467-021-23660-5.pdf
https://discovery.ucl.ac.uk/id/eprint/10129770/

المؤلفون: Thomas, JR, LaCombe, J, Long, R, Lana-Elola, E, Watson-Scales, S, Wallace, JM, Fisher, EMC, Tybulewicz, VLJ, Roper, RJ

المصدر: Bone , Article 115367. (2020) (In press).

مصطلحات موضوعية: Developmental modeling, Genetic animal models, Osteoporosis, Sexual dimorphism, Skeletal abnormalities, Trisomy 21

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10095766/1/1-s2.0-S8756328220301472-main.pdf; https://discovery.ucl.ac.uk/id/eprint/10095766/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10095766/1/1-s2.0-S8756328220301472-main.pdf
https://discovery.ucl.ac.uk/id/eprint/10095766/

المؤلفون: Ahlfors, H, Anyanwu, N, Pakanavicius, E, Dinischiotu, N, Lana-Elola, E, Watson-Scales, S, Tosh, J, Wiseman, F, Briscoe, J, Page, K, Fisher, EMC, Tybulewicz, VLJ

المصدر: 12 ; 1

مصطلحات موضوعية: Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, TC1 MOUSE MODEL, CRITICAL REGION, REORGANIZATION, CHROMOSOME-21, DYSFUNCTION, DYNAMICS, MEMORY, Animals, Disease Models, Animal, Down Syndrome, Fibroblasts, Gene Expression, Gene Expression Profiling, Genome, Genotype, Hippocampus, Mice, Multigene Family, Phenotype

Relation: Nature Communications; http://hdl.handle.net/10044/1/71256

الاتاحة: http://hdl.handle.net/10044/1/71256
https://doi.org/10.1038/s41467-019-10129-9

المؤلفون: Watson-Scales, S, Kalmar, B, Lana-Elola, E, Gibbins, D, La Russa, F, Wiseman, F, Williamson, M, Saccon, R, Slender, A, Olerinyova, A, Mahmood, R, Nye, E, Cater, H, Wells, S, Yu, Y, Bennett, D, Greensmith, L, Fisher, E, Tybulewicz, V

Relation: https://ora.ox.ac.uk/objects/uuid:ab54643c-78c0-4655-a111-03ff447b8a37; https://doi.org/10.1371/journal.pgen.1007383

الاتاحة: https://doi.org/10.1371/journal.pgen.1007383
https://ora.ox.ac.uk/objects/uuid:ab54643c-78c0-4655-a111-03ff447b8a37

المؤلفون: Dekker, AD, Vermeiren, Y, Albac, C, Lana-Elola, E, Watson-Scales, S, Gibbins, D, Aerts, T, Van Dam, D, Fisher, EMC, Tybulewicz, VLJ, Potier, M-C, De Deyn, PP

المصدر: Neurobiology of Disease , 105 pp. 235-244. (2017)

مصطلحات موضوعية: Aging, Dopamine, Down syndrome, Dp1Tyb, Monoamines, Mouse models, Noradrenaline, RP-HPLC, Serotonin, Ts65Dn

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/1561227/1/1-s2.0-S0969996117301341-main_AcceptedManuscript.pdf; https://discovery.ucl.ac.uk/id/eprint/1561227/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/1561227/1/1-s2.0-S0969996117301341-main_AcceptedManuscript.pdf
https://discovery.ucl.ac.uk/id/eprint/1561227/

المؤلفون: Lana-Elola, E, Watson-Scales, S, Slender, A, Gibbins, D, Martineau, A, Douglas, C, Mohun, T, Fisher, EM, Tybulewicz, VLJ

المصدر: eLife , 5 , Article e11614. (2016)

مصطلحات موضوعية: Down syndrome, chromosome engineering, congenital heart defects, developmental biology, human biology, medicine, mouse, mouse genetics, stem cells

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/1478106/1/Genetic%20dissection%20of%20Down%20syndrome-associated%20congenital%20heart%20defects%20using%20a%20new%20mouse%20mapping%20panel.pdf; https://discovery.ucl.ac.uk/id/eprint/1478106/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/1478106/1/Genetic%20dissection%20of%20Down%20syndrome-associated%20congenital%20heart%20defects%20using%20a%20new%20mouse%20mapping%20panel.pdf
https://discovery.ucl.ac.uk/id/eprint/1478106/

المؤلفون: Haas, MA, Bell, D, Slender, A, Lana-Elola, E, Watson-Scales, S, Fisher, EMC, Tybulewicz, VLJ, Guillemot, F

المصدر: Plos One , 8 (10) , Article e78561. (2013)

وصف الملف: application/pdf; other

Relation: https://discovery.ucl.ac.uk/id/eprint/1421006/1/journal.pone.0078561.pdf; https://discovery.ucl.ac.uk/id/eprint/1421006/2/journal.pone.0078561.g001.tif; https://discovery.ucl.ac.uk/id/eprint/1421006/3/journal.pone.0078561.g002.tif; https://discovery.ucl.ac.uk/id/eprint/1421006/4/journal.pone.0078561.g003.tif; https://discovery.ucl.ac.uk/id/eprint/1421006/5/journal.pone.0078561.g004.tif; https://discovery.ucl.ac.uk/id/eprint/1421006/6/journal.pone.0078561.g005.tif; https://discovery.ucl.ac.uk/id/eprint/1421006/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/1421006/1/journal.pone.0078561.pdf
https://discovery.ucl.ac.uk/id/eprint/1421006/2/journal.pone.0078561.g001.tif
https://discovery.ucl.ac.uk/id/eprint/1421006/3/journal.pone.0078561.g002.tif
https://discovery.ucl.ac.uk/id/eprint/1421006/4/journal.pone.0078561.g003.tif
https://discovery.ucl.ac.uk/id/eprint/1421006/5/journal.pone.0078561.g004.tif
https://discovery.ucl.ac.uk/id/eprint/1421006/6/journal.pone.0078561.g005.tif
https://discovery.ucl.ac.uk/id/eprint/1421006/

المؤلفون: Lana-Elola, E, Tylzanowski, P, Takatalo, M, Alakurtti, K, Veistinen, L, Mitsiadis, T A, Graf, D, Rice, R, Luyten, F P, Rice, D P

المصدر: Lana-Elola, E; Tylzanowski, P; Takatalo, M; Alakurtti, K; Veistinen, L; Mitsiadis, T A; Graf, D; Rice, R; Luyten, F P; Rice, D P (2011). Noggin null allele mice exhibit a microform of holoprosencephaly. Human Molecular Genetics, 20(20):4005-4015.

مصطلحات موضوعية: Institute of Oral Biology, 610 Medicine & health

وصف الملف: application/pdf

Relation: https://www.zora.uzh.ch/id/eprint/50355/1/Lana-Elola_Graf_et_al_2011_Human_Molecular_Genetics_2011PMID21821669_ZORA_2011_oct_26.pdf; https://www.zora.uzh.ch/id/eprint/50355/2/Lana_Elola_et_al_Graf_Autorenpdf_PMID21821669_Holopro_July_2011.pdf; info:pmid/21821669; urn:issn:0964-6906

الاتاحة: https://www.zora.uzh.ch/id/eprint/50355/
https://www.zora.uzh.ch/id/eprint/50355/2/Lana_Elola_et_al_Graf_Autorenpdf_PMID21821669_Holopro_July_2011.pdf
https://doi.org/10.1093/hmg/ddr329

المؤلفون: Rice, D. P. C., Connor, E. C., Veltmaat, J. M., Lana-Elola, E., Veistinen, L., Tanimoto, Y., Bellusci, S., Rice, R.

المصدر: Human Molecular Genetics ; volume 19, issue 17, page 3457-3467 ; ISSN 0964-6906 1460-2083

الاتاحة: https://doi.org/10.1093/hmg/ddq258
http://academic.oup.com/hmg/article-pdf/19/17/3457/1971730/ddq258.pdf

المؤلفون: Greene, Nicholas D. E., Copp, Andrew J., Andoniadou, Cynthia L., Cannavo, Claudia, Cleverley, K., Tosh, J. L., Noy, S., Lana-Elola, E., Tybulewicz, V., Fisher, E. M. C., Wiseman, F. K., Calderon, Lesly, Weiss, Felix D, Carroll, Thomas, Irvine, Elaine E., Dharmalingam, Gopuraja, Tossell, Kyoko, De Paola, Vincenzo, Whilding, Chad, Ungless, Mark A.

المصدر: Genetics Research; Jan2019, Vol. 101, pN.PAG-N.PAG, 5p

مصطلحات موضوعية: HUMAN chromosome 21, MAMMAL genetics, COHESINS, ALZHEIMER'S disease, FIBROBLASTS

المؤلفون: Dunlevy, L, Bennett, M, Slender, A, Lana-Elola, E, Tybulewicz, VL, Fisher, EMC, Mohun, T

المصدر: 295 ; 287

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, Down syndrome, Mouse model, 3D modelling, AVSD, COMMON ATRIOVENTRICULAR JUNCTION, VENTRICULAR SEPTAL-DEFECT, SYNDROME PHENOTYPES, CRITICAL REGION, TRISOMY 16, HEART, CHROMOSOME-21, ANOMALIES, GENE, HUMAN-CHROMOSOME-21, Abnormalities, Multiple, Animals, Aorta, Chromosomes, Human, Pair 21, Disease Models, Animal, Embryo, Mammalian, Endocardial Cushion Defects

Relation: CARDIOVASCULAR RESEARCH; http://hdl.handle.net/10044/1/58002; https://dx.doi.org/10.1093/cvr/cvq193

الاتاحة: http://hdl.handle.net/10044/1/58002
https://doi.org/10.1093/cvr/cvq193

المؤلفون: Hajihosseini, M.K., de Langhe, S., Lana-Elola, E., Morrison, H., Sparshott, N., Kelly, R.G., Sharpe, J., Rice, D., Bellusci, S.

المساهمون: Institut de Biologie du Développement de Marseille (IBDM), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1044-7431.

مصطلحات موضوعية: [SDV.BC]Life Sciences [q-bio]/Cellular Biology

Relation: hal-00311129; https://hal.science/hal-00311129

الاتاحة: https://hal.science/hal-00311129

المؤلفون: Tybulewicz, V., Wiseman, F., Watson, S., Lana Elola, E., Ruparelia, A., Sheppard, O., Slender, A., Fisher, E.

المصدر: Proceedings of the Physiological Society; 2011, Vol. 22, p70P-71P, 2p