نتائج البحث - "Greensmith, L."

المساهمون: Pennuto, M., Pradat, P. F., Soraru, G., Greensmith, L., Basso, M., Bertolotti, M., de Carvalho, M., Fabris, G., Fenu, S., Fratta, P., Fischbeck, K., Gozes, I., Katsuno, M., Malik, B., Maclean, A., Meyertholen, E., Pilati, N., Poletti, A., Querin, G., Rinaldi, C., Ronzitti, G., Salvatella, X., Slowe, K., Vissing, J., Weber, M., Weydt, P., Zampedri, L., Zanovello, M., Zuccaro, E.

مصطلحات موضوعية: Androgen receptor, Clinical trial, ENMC, Kennedy disease, Patient registry, SBMA

Relation: info:eu-repo/semantics/altIdentifier/pmid/38552412; volume:38; firstpage:8; lastpage:19; numberofpages:12; journal:NEUROMUSCULAR DISORDERS; https://hdl.handle.net/11577/3514027; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85189448050

الاتاحة: https://hdl.handle.net/11577/3514027
https://doi.org/10.1016/j.nmd.2024.03.003

View record in BASE

4

Academic Journal

An optogenetic cell therapy to restore control of target muscles in an aggressive mouse model of amyotrophic lateral sclerosis

المؤلفون: Bryson, JB, Kourgiantaki, A, Jiang, D, Demosthenous, A, Greensmith, L

المصدر: eLife , 12 , Article RP88250. (2024)

مصطلحات موضوعية: ALS, Amyotrophic Lateral Sclerosis, cell transplant, motor neurons, mouse, optogenetics, paralysis, regenerative medicine, stem cells, Animals, Mice, Humans, Muscle, Skeletal, Cell- and Tissue-Based Therapy, Disease Models, Animal

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/10186337/1/elife-88250-v1.pdf; https://discovery.ucl.ac.uk/id/eprint/10186337/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10186337/1/elife-88250-v1.pdf
https://discovery.ucl.ac.uk/id/eprint/10186337/

View record in BASE

5

Academic Journal

Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population

المؤلفون: Zanovello, M, Ibanez, K, Brown, A-L, Sivakumar, P, Bombaci, A, Santos, L, van Vugt, JJFA, Narzisi, G, Karra, R, Scholz, SW, Ding, J, Gibbs, JR, Chio, A, Dalgard, C, Weisburd, B, Hanna, MG, Greensmith, L, Phatnani, H, Veldink, JH, Traynor, BJ, Polke, J, Houlden, H, Fratta, P, Tucci, A

مصطلحات موضوعية: androgen receptor, whole-genome sequencing, bioinformatics, population genetics, spinal and bulbar muscular atrophy

وصف الملف: 2723 - 2729

Relation: BRAIN; https://qmro.qmul.ac.uk/xmlui/handle/123456789/89471

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/89471
https://doi.org/10.1093/brain/awad050

View record in BASE

Full Text Finder

6

Academic Journal

AR cooperates with SMAD4 to maintain skeletal muscle homeostasis

المؤلفون: Forouhan M., Lim W. F., Zanetti-Domingues L. C., Tynan C. J., Roberts T. C., Malik B., Manzano R., Speciale A. A., Ellerington R., Garcia-Guerra A., Fratta P., Soraru G., Greensmith L., Pennuto M., Wood M. J. A., Rinaldi C.

المساهمون: Forouhan, M., Lim, W. F., Zanetti-Domingues, L. C., Tynan, C. J., Roberts, T. C., Malik, B., Manzano, R., Speciale, A. A., Ellerington, R., Garcia-Guerra, A., Fratta, P., Soraru, G., Greensmith, L., Pennuto, M., Wood, M. J. A., Rinaldi, C.

مصطلحات موضوعية: Androgen receptor, Androgen, Muscle atrophy, SBMA, TGFβ pathway, Transcriptional cooperativity, Animal, Homeostasi, Mice, Transgenic, Muscle, Skeletal, Muscular Atrophy, Spinal, Receptors

Relation: info:eu-repo/semantics/altIdentifier/pmid/35522298; info:eu-repo/semantics/altIdentifier/wos/WOS:000791627000001; volume:143; issue:6; firstpage:713-731; lastpage:731; journal:ACTA NEUROPATHOLOGICA; http://hdl.handle.net/11577/3449498; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85129521104

الاتاحة: http://hdl.handle.net/11577/3449498
https://doi.org/10.1007/s00401-022-02428-1

View record in BASE

7

Academic Journal

Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles

المؤلفون: Suetterlin, KJ, Männikkö, R, Matthews, E, Greensmith, L, Hanna, MG, Bostock, H, Tan, SV

المصدر: Neuromuscular Disorders (2022) (In press).

مصطلحات موضوعية: Muscle Velocity Recovery Cycles (MVRCs), Excitability, ClC-1, Skeletal Muscle Channelopathies, Mouse modelTranslational gap

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10144834/1/1-s2.0-S0960896622000633-main.pdf; https://discovery.ucl.ac.uk/id/eprint/10144834/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10144834/1/1-s2.0-S0960896622000633-main.pdf
https://discovery.ucl.ac.uk/id/eprint/10144834/

View record in BASE

8

Academic Journal

Enhanced Expression of TRAP1 Protects Mitochondrial Function in Motor Neurons under Conditions of Oxidative Stress

المؤلفون: Clarke, BE, Kalmar, B, Greensmith, L

المصدر: International Journal of Molecular Sciences , 23 (3) , Article 1789. (2022)

مصطلحات موضوعية: TRAP1, motor neuron, mitochondria, oxidative stress

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/10143737/1/Clarke_ijms-23-01789-v2.pdf; https://discovery.ucl.ac.uk/id/eprint/10143737/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10143737/1/Clarke_ijms-23-01789-v2.pdf
https://discovery.ucl.ac.uk/id/eprint/10143737/

View record in BASE

9

Academic Journal

AR cooperates with SMAD4 to maintain skeletal muscle homeostasis

المؤلفون: Forouhan M, Lim WF, Zanetti Domingues LC, Tynan CJ, Roberts TC, Malik B, Manzano R, Speciale AA, Ellerington R, Garcia-Guerra A, Fratta P, Sorarú G, Greensmith L, Pennuto M, Wood MJA, Rinaldi C

Relation: Science and Technology Facilities Council (2007- ); Central Laser Facility (1977- ); CLF - Science-Lasers for Science; http://purl.org/net/epubs/work/52302749

الاتاحة: http://purl.org/net/epubs/work/52302749

View record in BASE

10

Academic Journal

Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification

المؤلفون: Schottlaender L. V., Abeti R., Jaunmuktane Z., Macmillan C., Chelban V., O'Callaghan B., McKinley J., Maroofian R., Efthymiou S., Athanasiou-Fragkouli A., Forbes R., Soutar M. P. M., Livingston J. H., Kalmar B., Swayne O., Hotton G., Groppa S., Karashova B. M., Nachbauer W., Boesch S., Arning L., Timmann D., Cormand B., Perez-Duenas B., Di Rosa G., Goraya J. S., Sultan T., Mine J., Avdjieva D., Kathom H., Tincheva R., Banu S., Pineda-Marfa M., Veggiotti P., Ferrari M. D., Verrotti A., Marseglia G., Savasta S., Garcia-Silva M., Ruiz A. M., Garavaglia B., Borgione E., Portaro S., Sanchez B. M., Boles R., Papacostas S., Vikelis M., Papanicolaou E. Z., Dardiotis E., Maqbool S., Ibrahim S., Kirmani S., Rana N. N., Atawneh O., Koutsis G., Breza M., Mangano S., Scuderi C., Morello G., Stojkovic T., Zollo M., Heimer G., Dauvilliers Y. A., Striano P., Al-Khawaja I., Al-Mutairi F., Sherifa H., Pittman A., Mendes de Oliveira J. R., de Grandis M., Richard-Loendt A., Launchbury F., Althonayan J., McDonnell G., Carr A., Khan S., Beetz C., Bisgin A., Tug Bozdogan S., Begtrup A., Torti E., Greensmith L., Giunti P., Morrison P. J., Brandner S., Aurrand-Lions M., Houlden H.

المساهمون: Schottlaender L.V., Abeti R., Jaunmuktane Z., Macmillan C., Chelban V., O'Callaghan B., McKinley J., Maroofian R., Efthymiou S., Athanasiou-Fragkouli A., Forbes R., Soutar M.P.M., Livingston J.H., Kalmar B., Swayne O., Hotton G., Groppa S., Karashova B.M., Nachbauer W., Boesch S., Arning L., Timmann D., Cormand B., Perez-Duenas B., Di Rosa G., Goraya J.S., Sultan T., Mine J., Avdjieva D., Kathom H., Tincheva R., Banu S., Pineda-Marfa M., Veggiotti P., Ferrari M.D., Verrotti A., Marseglia G., Savasta S., Garcia-Silva M., Ruiz A.M., Garavaglia B., Borgione E., Portaro S., Sanchez B.M., Boles R., Papacostas S., Vikelis M., Papanicolaou E.Z., Dardiotis E., Maqbool S., Ibrahim S., Kirmani S., Rana N.N., Atawneh O., Koutsis G., Breza M., Mangano S., Scuderi C., Morello G., Stojkovic T., Zollo M., Heimer G., Dauvilliers Y.A., Striano P., Al-Khawaja I., Al-Mutairi F., Sherifa H., Pittman A., Mendes de Oliveira J.R., de Grandis M., Richard-Loendt A., Launchbury F., Althonayan J., McDonnell G., Carr A., Khan S., Beetz C., Bisgin A., Tug Bozdogan S., Begtrup A., Torti E., Greensmith L., Giunti P., Morrison P.J., Brandner S., Aurrand-Lions M., Houlden H.

مصطلحات موضوعية: Fahr disease, familial idiopathic basal ganglia calcification, JAM2, JAM3, knock out mouse model, MYORG, OCLN, primary familial brain calcification, recessive brain calcification, SLC20A2

Relation: info:eu-repo/semantics/altIdentifier/pmid/32142645; info:eu-repo/semantics/altIdentifier/wos/WOS:000519101800017; volume:106; issue:3; firstpage:412; lastpage:421; numberofpages:10; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/10447/407084

الاتاحة: http://hdl.handle.net/10447/407084
https://doi.org/10.1016/j.ajhg.2020.02.007

View record in BASE

11

Academic Journal

Automated and unbiased discrimination of ALS from control tissue at single cell resolution

المؤلفون: Hagemann C, Tyzack GE, Taha DM, Devine H, Greensmith L, Newcombe J, Patani R, Serio A, Luisier R

المصدر: Brain Pathology, July 2021

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/301377; https://eprints.ncl.ac.uk/fulltext.aspx?url=301377/DC0AFBF6-EDED-4C1D-B178-B34FABF4FBB0.pdf&pub_id=301377

الاتاحة: https://eprints.ncl.ac.uk/301377

View record in BASE

12

Academic Journal

Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosis

المؤلفون: Magen, I, Yacovzada, NS, Yanowski, E, Coenen-Stass, A, Grosskreutz, J, Lu, C-H, Greensmith, L, Malaspina, A, Fratta, P, Hornstein, E

المصدر: Nature Neuroscience , 24 (11) pp. 1534-1541. (2021)

وصف الملف: text; image

View record in BASE

13

Academic Journal

An iPSC model of hereditary sensory neuropathy-1 reveals L-serine-responsive deficits in neuronal ganglioside composition and axoglial interactions

المؤلفون: Clark, AJ, Kugathasan, U, Baskozos, G, Priestman, DA, Fugger, N, Lone, MA, Othman, A, Chu, KH, Blesneac, I, Wilson, ER, Laurà, M, Kalmar, B, Greensmith, L, Hornemann, T, Platt, FM, Reilly, MM, Bennett, DL

المصدر: Cell Reports Medicine , 2 (7) , Article 10034. (2021)

مصطلحات موضوعية: hereditary sensory neuropathy type 1, HSN1, serine palmitoyltransferase, SPT, serine palmitoyltransferase long-chain base subunit 1, SPTLC1, 1-deoxySLBs, DSBs, sphingolipid, ganglioside, sensory neuron, myelin, axon, l-serine

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10132384/1/1-s2.0-S2666379121001944-main.pdf; https://discovery.ucl.ac.uk/id/eprint/10132384/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10132384/1/1-s2.0-S2666379121001944-main.pdf
https://discovery.ucl.ac.uk/id/eprint/10132384/

View record in BASE

14

Academic Journal

Regional Differences in Heat Shock Protein 25 Expression in Brain and Spinal Cord Astrocytes of Wild-Type and SOD1 (G93A) Mice

المؤلفون: San Gil, R, Clarke, BE, Ecroyd, H, Kalmar, B, Greensmith, L

المصدر: Cell , 10 (5) , Article 1257. (2021)

مصطلحات موضوعية: heat shock response, heat shock protein 27, glia, astrocytes, amyotrophic lateral sclerosis, motor neuron disease

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10128324/3/Clarke_Regional%20Differences%20in%20Heat%20Shock%20Protein%2025%20Expression%20in%20Brain%20and%20Spinal%20Cord%20Astrocytes%20of%20Wild-Type%20and%20SOD1%20%28G93A%29%20Mice_VoR.pdf; https://discovery.ucl.ac.uk/id/eprint/10128324/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10128324/3/Clarke_Regional%20Differences%20in%20Heat%20Shock%20Protein%2025%20Expression%20in%20Brain%20and%20Spinal%20Cord%20Astrocytes%20of%20Wild-Type%20and%20SOD1%20%28G93A%29%20Mice_VoR.pdf
https://discovery.ucl.ac.uk/id/eprint/10128324/

View record in BASE

15

Academic Journal

Ageing Contributes to Phenotype Transition in a Mouse Model of Periodic Paralysis

المؤلفون: Suetterlin, K, Tan, S, Männikkö, R, Phadke, R, Orford, MR, Eaton, S, Sayer, A, Grounds, M, Matthews, E, Greensmith, L, Hanna, M

المصدر: JCSM Rapid Communications , 4 (2) pp. 245-259. (2021)

مصطلحات موضوعية: Ageing, Channelopathy, Periodic paralysis, Sarcopenia, Skeletal muscle, Ion channels

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10125668/7/Suetterlin_rco2.41.pdf; https://discovery.ucl.ac.uk/id/eprint/10125668/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10125668/7/Suetterlin_rco2.41.pdf
https://discovery.ucl.ac.uk/id/eprint/10125668/

View record in BASE

16

Academic Journal

The altered expression of neurofilament in mouse models and patients with spinal muscular atrophy

المؤلفون: Spicer, C, Lu, C-H, Catapano, F, Scoto, M, Zaharieva, I, Malaspina, A, Morgan, JE, Greensmith, L, Muntoni, F, Zhou, H

المصدر: Annals of Clinical and Translational Neurology (2021) (In press).

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10124085/1/2021-Spicer-NF-SMA-ACTN.pdf; https://discovery.ucl.ac.uk/id/eprint/10124085/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10124085/1/2021-Spicer-NF-SMA-ACTN.pdf
https://discovery.ucl.ac.uk/id/eprint/10124085/

View record in BASE

17

Academic Journal

Ageing contributes to phenotype transition in a mouse model of periodic paralysis

المؤلفون: Suetterlin, KJ, Tan, SV, Mannikko, R, Phadke, R, Orford, M, Eaton, S, Sayer, AA, Grounds, MD, Matthews, E, Greensmith, L, Hanna, MG

وصف الملف: application/pdf; application/zip; image/png; application/vnd.ms-excel; application/vnd.openxmlformats-officedocument.wordprocessingml.document

Relation: https://openaccess.sgul.ac.uk/id/eprint/113830/3/rco2.41.pdf; https://openaccess.sgul.ac.uk/id/eprint/113830/8/rco2_41-sup-0001-figure%20s1.zip; https://openaccess.sgul.ac.uk/id/eprint/113830/9/rco2_41-sup-0002-figure%20s2.png; https://openaccess.sgul.ac.uk/id/eprint/113830/15/rco2_41-sup-0003-data_s1.xlsx; https://openaccess.sgul.ac.uk/id/eprint/113830/1/JCSM_Comms_Revised%20RCO2-D-20-00020%2002032021.docx; Suetterlin, KJ; Tan, SV; Mannikko, R; Phadke, R; Orford, M; Eaton, S; Sayer, AA; Grounds, MD; Matthews, E; Greensmith, L; et al. Suetterlin, KJ; Tan, SV; Mannikko, R; Phadke, R; Orford, M; Eaton, S; Sayer, AA; Grounds, MD; Matthews, E; Greensmith, L; Hanna, MG (2021) Ageing contributes to phenotype transition in a mouse model of periodic paralysis. JCSM Rapid Communications, 4 (2). pp. 245-259. ISSN 2617-1619 https://doi.org/10.1002/rco2.41 SGUL Authors: Matthews, Emma Louise