Sue Shackleton - Publications, H-index & Citations

Sue Shackleton

university of leicester

19H指数

49论文数

2.8K被引数

收录论文 15

发表时间

Remembering Andrew Fry (1966-2024)

JOURNAL OF CELL SCIENCE

IF3.6

2024-09-06

OAAI

Bayliss, Richard; Fry, Tim; Mahen, Robert; Shackleton, Sue; Tanaka, Kayoko

SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-27

493

OAAI

Haque, Farhana; Lloyd, David J.; Smallwood, Dawn T.; Dent, Carolyn L.; Shanahan, Catherine M.; Fry, Andrew M.; Trembath, Richard C.; Shackleton, Sue

RAC1 induces nuclear alterations through the LINC complex to enhance melanoma invasiveness

MOLECULAR BIOLOGY OF THE CELL

IF2.7

2020-12-01

OAAI

Colon-Bolea, Paula; Garcia-Gomez, Rocio; Shackleton, Sue; Crespo, Piero; Bustelo, Xose R.; Casar, Berta

Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells

CURRENT BIOLOGY

IF7.5

2017-10-01

118

OAAI

Gimpel, Petra; Lee, Yin Loon; Sobota, Radoslaw M.; Calvi, Alessandra; Koullourou, Victoria; Patel, Rutti; Mamchaoui, Kamel; Nedelec, Francois; Shackleton, Sue; Schmoranzer, Jan; Burke, Brian; Cadot, Bruno; Gomes, Edgar R.

Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis

HUMAN MOLECULAR GENETICS

IF3.2

2017-04-07

OAAI

Zhou, Can; Li, Chen; Zhou, Bin; Sun, Huaqin; Koullourou, Victoria; Holt, Ian; Puckelwartz, Megan J.; Warren, Derek T.; Hayward, Robert; Lin, Ziyuan; Zhang, Lin; Morris, Glenn E.; McNally, Elizabeth M.; Shackleton, Sue; Rao, Li; Shanahan, Catherine M.; Zhang, Qiuping

Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelope

NATURE COMMUNICATIONS

IF15.7

2016-03-30

OAAI

Mikolcevic, Petra; Isoda, Michitaka; Shibuya, Hiroki; del Barco Barrantes, Ivan; Igea, Ana; Suja, Jose A.; Shackleton, Sue; Watanabe, Yoshinori; Nebreda, Angel R.

Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization

PLOS GENETICS

IF3.7

2014-09-11

159

OAAI

Meinke, Peter; Mattioliz, Elisabetta; Haque, Farhana; Antoku, Susumu; Columbaro, Marta; Straatman, Kees R.; Worman, Howard J.; Gundersen, Gregg G.; Lattanzi, Giovanna; Wehnert, Manfred; Shackleton, Sue

A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus

HUMAN MOLECULAR GENETICS

IF3.2

2013-02-12

OAAI

Watkins, Rachel J.; Patil, Rajashree; Goult, Benjamin T.; Thomas, Mervyn G.; Gottlob, Irene; Shackleton, Sue

MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy

FASEB JOURNAL

IF4.2

2011-08-12

PREAI

Sylvius, Nicolas; Bonne, Gisele; Straatman, Kees; Reddy, Thimma; Gant, Timothy W.; Shackleton, Sue

Mammalian SUN Protein Interaction Networks at the Inner Nuclear Membrane and Their Role in Laminopathy Disease Processes

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2010-01-01

283

OAAI

Haque, Farhana; Mazzeo, Daniela; Patel, Jennifer T.; Smallwood, Dawn T.; Ellis, Juliet A.; Shanahan, Catherine M.; Shackleton, Sue

Hutchinson-Gilford progeria syndrome:: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2007-06-01

PREAI

Mazereeuw-Hautier, J.; Wilson, L. C.; Mohammed, S.; Smallwood, D.; Shackleton, S.; Atherton, D. J.; Harper, J. I.

Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotype -: art. no. e36

JOURNAL OF MEDICAL GENETICS

IF3.7

2005-06-01

112

OAAI

Shackleton, S; Smallwood, DT; Clayton, P; Wilson, LC; Agarwal, AK; Garg, A; Trembath, RC

Role of two dileucine-like motifs in insulin receptor anchoring to microvilli

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2002-11-01

PREAI

Shackleton, S; Hamer, I; Foti, M; Zumwald, N; Maeder, C; Carpentier, JL

Lamin A/C gene -: Sex-determined expression of mutations in dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy

DIABETES

IF7.5

2000-11-01

152

OAAI

Vigouroux, C; Magré, J; Vantyghem, MC; Bourut, C; Lascols, O; Shackleton, S; Lloyd, DJ; Guerci, B; Padova, G; Valensi, P; Grimaldi, A; Piquemal, R; Touraine, P; Trembath, RC; Capeau, J

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

NATURE GENETICS

IF31.8

2000-02-01

601

PREAI

Shackleton, S; Lloyd, DJ; Jackson, SNJ; Evans, R; Niermeijer, MF; Singh, BM; Schmidt, H; Brabant, G; Kumar, S; Durrington, PN; Gregory, S; O'Rahilly, S; Trembath, RC

研究方向