Works matching DE "SPECTRIN"

Results: 304

Characterization of Spectrin Family Genes and Their Evolutionary Roles in Domestication and Breeding of the Silkworm Bombyx mori.

Published in:

Insects (2075-4450), 2025, v. 16, n. 6, p. 556, doi. 10.3390/insects16060556

By:

Lu, Kunpeng;
Zhan, Chengyu;
Shen, Jianghong;
Zhi, Chao;
Deng, Jun;
Lai, Kerui;
Han, Minjin;
Hu, Hai;
Tong, Xiaoling;
Dai, Fangyin

Publication type:

Article

Loss of cooperative function of transforming growth factor-β signaling proteins, smad3 with embryonic liver fodrin, aβ-spectrin, in primary biliary cirrhosis.

Published in:

Liver International, 2004, v. 24, n. 6, p. 637, doi. 10.1111/j.1478-3231.2004.0958.x

By:

Mishra, Bibhuti;
Yi Tang;
Katuri, Varalakshmi;
Fleury, Tom;
Said, Anan H.;
Rashid, Asif;
Jogunoori, Wilma;
Mishra, Lopa

Publication type:

Article

Changes in localization and expression levels of Shroom2 and spectrin contribute to variation in amphibian egg pigmentation patterns.

Published in:

Development Genes & Evolution, 2009, v. 219, n. 6, p. 319, doi. 10.1007/s00427-009-0292-x

By:

Chanjae Lee;
Minh-Phuong Le;
Cannatella, David;
Wallingford, John B.

Publication type:

Article

Changes in caspase activities post mortem and their relationships to shear force in porcine longissumus muscle.

Published in:

Journal of Animal Science, 2006, v. 84, p. 37

By:

Kemp, C. M.;
Bardsley, R. G.;
Parr, T.

Publication type:

Article

A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.

Published in:

Cerebellum, 2018, v. 17, n. 3, p. 276, doi. 10.1007/s12311-017-0893-2

By:

Al-Muhaizea, Mohammad A.;
AlMutairi, Faten;
Almass, Rawan;
AlHarthi, Safinaz;
Aldosary, Mazhor S.;
Alsagob, Maysoon;
AlOdaib, Ali;
Colak, Dilek;
Kaya, Namik

Publication type:

Article

A Family with Spinocerebellar Ataxia Type 5 Found to Have a Novel Missense Mutation within a SPTBN2 Spectrin Repeat.

Published in:

Cerebellum, 2013, v. 12, n. 2, p. 162, doi. 10.1007/s12311-012-0408-0

By:

Cho, Ellen;
Fogel, Brent

Publication type:

Article

Competition between myosin II and β<sub>H</sub>-spectrin regulates cytoskeletal tension.

Published in:

eLife, 2023, p. 1, doi. 10.7554/eLife.84918

By:

Ibar, Consuelo;
Chinthalapudi, Krishna;
Heissler, Sarah M.;
Irvine, Kenneth D.

Publication type:

Article

Functional characterization of protein 4.1 homolog in amphioxus: Defining a cryptic spectrin-actin-binding site.

Published in:

Scientific Reports, 2013, p. 1, doi. 10.1038/srep02873

By:

Lixia Wang;
Yuan Wang;
Zhaohe Li;
Zhan Gao;
Shicui Zhang

Publication type:

Article

SYNE1-related autosomal recessive cerebellar ataxia, congenital cerebellar hypoplasia, and cognitive impairment.

Published in:

Clinics & Practice, 2018, v. 8, n. 3, p. 91, doi. 10.4081/cp.2018.1071

By:

Swan, Lauren;
Cardinal, John;
Coman, David

Publication type:

Article

Multi-domain interaction mediated strength-building in human α-actinin dimers unveiled by direct single-molecule quantification.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50430-w

By:

Zhang, Yuhang;
Du, Jingyi;
Liu, Xian;
Shang, Fei;
Deng, Yunxin;
Ye, Jiaqing;
Wang, Yukai;
Yan, Jie;
Chen, Hu;
Yu, Miao;
Le, Shimin

Publication type:

Article

Mechanically induced topological transition of spectrin regulates its distribution in the mammalian cell cortex.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49906-6

By:

Ghisleni, Andrea;
Bonilla-Quintana, Mayte;
Crestani, Michele;
Lavagnino, Zeno;
Galli, Camilla;
Rangamani, Padmini;
Gauthier, Nils C.

Publication type:

Article

Disorders of the erythrocyte membrane.

Published in:

Italian Journal of Medicine, 2015, v. 9, n. 4, p. 323, doi. 10.4081/itjm.2015.470

By:

Delicou, Sophia;
Xydaki, Aikaterini;
Kontaxi, Chryssanthi;
Maragkos, Konstantinos

Publication type:

Article

Important region in the β-spectrin C -terminus for spectrin tetramer formation.

Published in:

European Journal of Haematology, 2002, v. 68, n. 2, p. 73, doi. 10.1034/j.1600-0609.2002.01569.x

By:

Luo, Bing-Hao;
Mehboob, Shahila;
Hurtuk, Michael G;
Pipalia, N. H;
Fung, L. W.-M

Publication type:

Article

Association of the α‐spectrin R28H mutation with allele α<sup>LELY</sup> and with αI/αII domain haplotypes in three Brazilian families.

Published in:

European Journal of Haematology, 2000, v. 64, n. 1, p. 53, doi. 10.1034/j.1600-0609.2000.80217.x

By:

Bassères, Daniela S.;
Bordin, Silvana;
Costa, Fernando F.;
Saad, Sara T. O.

Publication type:

Article

Vincent J. Hearing, PhD.

Published in:

Pigment Cell & Melanoma Research, 2010, v. 23, n. 4, p. 571, doi. 10.1111/j.1755-148X.2010.00710.x

By:

Pawelek, John

Publication type:

Article

THERMAL DIELECTROSCOPY STUDY OF SUBMEMBRANE SPECTRIN NETWORK IN ANIMAL ERYTHROCYTES.

Published in:

Bulgarian Journal of Veterinary Medicine, 2014, v. 17, n. 3, p. 165

By:

PAARVANOVA, B.;
SLAVOV, T.;
IVANOV, V.;
IVANOV, I.

Publication type:

Article

Role of a Pdlim5:PalmD complex in directing dendrite morphology.

Published in:

Frontiers in Cellular Neuroscience, 2024, p. 1, doi. 10.3389/fncel.2024.1315941

By:

Srivastava, Yogesh;
Donta, Maxsam;
Mireles, Lydia L.;
Paulucci-Holthauzen, Adriana;
Waxham, M. Neal;
McCrea, Pierre D.

Publication type:

Article

Nodal Dynamics after In Vivo Rescue of βIV Spectrin Expression.

Published in:

Journal of Neuroscience, 2019, v. 39, n. 1, p. 15, doi. 10.1523/JNEUR0SCI.2149-18.2018

By:

Bacmeister, Clara Maria;
Thornton, Michael Andrew

Publication type:

Article

Reorganization of Destabilized Nodes of Ranvier in βIV Spectrin Mutants Uncovers Critical Timelines for Nodal Restoration and Prevention of Motor Paresis.

Published in:

Journal of Neuroscience, 2018, v. 38, n. 28, p. 6267, doi. 10.1523/JNEUROSCI.0515-18.2018

By:

Saifetiarova, Julia;
Qian Shi;
Paukert, Martin;
Masayuki Komada;
Bhat, Manzoor A.

Publication type:

Article

Glial βII Spectrin Contributes to Paranode Formation and Maintenance.

Published in:

Journal of Neuroscience, 2018, v. 38, n. 27, p. 6063, doi. 10.1523/JNEUROSCI.3647-17.2018

By:

Keiichiro Susuki;
Zollinger, Daniel R.;
Kae-Jiun Chang;
Chuansheng Zhang;
Yu-Mei Huang, Claire;
Chang-Ru Tsai;
Galiano, Mauricio R.;
Yanhong Liu;
Benusa, Savannah D.;
Yermakov, Leonid M.;
Griggs, Ryan B.;
Dupree, Jeffrey L.;
Rasband, Matthew N.

Publication type:

Article

An αll Spectrin-Based Cytoskeleton Protects Large-Diameter Myelinated Axons from Degeneration.

Published in:

Journal of Neuroscience, 2017, v. 37, n. 47, p. 11323, doi. 10.1523/JNEUROSCI.2113-17.2017

By:

Yu-Mei Huang, Claire;
Chuansheng Zhang;
Zollinger, Daniel R.;
Leterrier, Christophe;
Rasband, Matthew N.

Publication type:

Article

αll Spectrin Forms a Periodic Cytoskeleton at the Axon Initial Segment and Is Required for Nervous System Function.

Published in:

Journal of Neuroscience, 2017, v. 37, n. 47, p. 11311, doi. 10.1523/JNEUROSCI.2112-17.2017

By:

Yu-Mei Huang, Claire;
Chuansheng Zhang;
Szu-Yu Ho, Tammy;
Oses-Prieto, Juan;
Burlingame, Alma L.;
Lalonde, Joshua;
Noebels, Jeffrey L.;
Leterrier, Christophe;
Rasband, Matthew N.

Publication type:

Article

This Week in The Journal.

Published in:

Journal of Neuroscience, 2017, v. 37, n. 27, p. i

By:

Esch, Teresa

Publication type:

Article

βIII Spectrin Is Necessary for Formation of the Constricted Neck of Dendritic Spines and Regulation of Synaptic Activity in Neurons.

Published in:

Journal of Neuroscience, 2017, v. 37, n. 27, p. 6442, doi. 10.1523/JNEUROSCI.3520-16.2017

By:

Efimova, Nadia;
Korobova, Farida;
Stankewich, Michael C.;
Moberly, Andrew H.;
Stolz, Donna B.;
Junling Wang;
Kashina, Anna;
Minghong Ma;
Svitkina, Tatyana

Publication type:

Article

Early and Late Loss of the Cytoskeletal Scaffolding Protein, Ankyrin G Reveals Its Role in Maturation and Maintenance of Nodes of Ranvier in Myelinated Axons.

Published in:

Journal of Neuroscience, 2017, v. 37, n. 10, p. 2524, doi. 10.1523/JNEUROSCI.2661-16.2017

By:

Saifetiarova, Julia;
Taylor, Anna M.;
Bhat, Manzoor A.

Publication type:

Article

Inositol Hexakisphosphate Kinase-3 Regulates the Morphology and Synapse Formation of Cerebellar Purkinje Cells via Spectrin/Adducin.

Published in:

Journal of Neuroscience, 2015, v. 35, n. 31, p. 11056, doi. 10.1523/JNEUROSCI.1069-15.2015

By:

Chenglai Fu;
Jing Xu;
Ruo-Jing Li;
Crawford, Joshua A.;
Khan, A. Basit;
Ma, Ting Martin;
Cha, Jiyoung Y.;
Snowman, Adele M.;
Pletnikov, Mikhail V.;
Snyder, Solomon H.

Publication type:

Article

Mutant β-III Spectrin Causes mGluR1α Mislocalization and Functional Deficits in a Mouse Model of Spinocerebellar Ataxia Type 5.

Published in:

Journal of Neuroscience, 2014, v. 34, n. 30, p. 9891, doi. 10.1523/JNEUROSCI.0876-14.2014

By:

Armbrust, Karen R.;
Xinming Wang;
Hathorn, Tyisha J.;
Cramer, Samuel W.;
Gang Chen;
Tao Zu;
Takashi Kangas;
Zink, Anastasia N.;
Öz, Gülin;
Ebner, Timothy J.;
Ranum, Laura P. W.

Publication type:

Article

Crystal structure of the amphiphysin-2 SH3 domain and its role in the prevention of dynamin ring formation.

Published in:

EMBO Journal, 1998, v. 17, n. 18, p. 5273, doi. 10.1093/emboj/17.18.5273

By:

Owen, D. J.;
Wigge, P.;
Vallis, Y.;
Moore, J. D. A.;
Evans, P. R.;
McMahon, H. T.

Publication type:

Article

Brain spectrin binding to the NMDA receptor is regulated by phosphorylation, calcium and calmodulin.

Published in:

EMBO Journal, 1998, v. 17, n. 14, p. 3931, doi. 10.1093/emboj/17.14.3931

By:

Wechsler, Aharon;
Teichberg, Vivian I.

Publication type:

Article

Early onset West syndrome with severe hypomyelination and coloboma-like optic discs in a girl with SPTAN1 mutation.

Published in:

Epilepsia (Series 4), 2012, v. 53, n. 6, p. e106, doi. 10.1111/j.1528-1167.2012.03437.x

By:

Writzl, Karin;
Primec, Zvonka Rener;
Stražišar, Barbara Gnidovec;
Osredkar, Damjan;
Pečarič-Meglič, Nuška;
Kranjc, Branka Stirn;
Nishiyama, Kiyomi;
Matsumoto, Naomichi;
Saitsu, Hirotomo

Publication type:

Article

Aggregation of spectrin and PKCθ is an early hallmark of fludarabine/mitoxantrone/dexamethasone-induced apoptosis in Jurkat T and HL60 cells.

Published in:

Molecular & Cellular Biochemistry, 2010, v. 339, n. 1/2, p. 63, doi. 10.1007/s11010-009-0370-4

By:

Dubielecka, Patrycja M.;
Grzybek, Michał;
Kolondra, Adam;
Jaźwiec, Bożena;
Draga, Anna;
Aleksandrowicz, Paulina;
Kołodziejczyk, Monika;
Serwotka, Anna;
Dolińska-Krajewska, Barbara;
Warchoł, Jerzy;
Kuliczkowski, Kazimierz;
Sikorski, Aleksander F.

Publication type:

Article

Osmotic Stress Alters the Intracellular Distribution of Non-erythroidal Spectrin (Fodrin) in Bovine Aortic Endothelial Cells.

Published in:

Journal of Membrane Biology, 2003, v. 192, n. 1, p. 9, doi. 10.1007/s00232-002-1060-2

By:

Sun, A. C.;
Levitan, I.

Publication type:

Article

Actin acting at the Golgi.

Published in:

Histochemistry & Cell Biology, 2013, v. 140, n. 3, p. 347, doi. 10.1007/s00418-013-1115-8

By:

Egea, Gustavo;
Serra-Peinado, Carla;
Salcedo-Sicilia, Laia;
Gutiérrez-Martínez, Enric

Publication type:

Article

αII-spectrin and βII-spectrin do not affect TGFβ1-induced myofibroblast differentiation.

Published in:

Cell & Tissue Research, 2018, v. 374, n. 1, p. 165, doi. 10.1007/s00441-018-2842-x

By:

Piersma, Bram;
Wouters, Olaf Y.;
Bank, Ruud A.

Publication type:

Article

Calpain inhibition prevents flotillin re-ordering and Src family activation during capacitation.

Published in:

Cell & Tissue Research, 2017, v. 369, n. 2, p. 395, doi. 10.1007/s00441-017-2591-2

By:

Maldonado-García, Deneb;
Salgado-Lucio, Monica;
Roa-Espitia, Ana;
Reyes-Miguel, Tania;
Hernández-González, Enrique

Publication type:

Article

Secretory cells in honeybee hypopharyngeal gland: polarized organization and age-dependent dynamics of plasma membrane.

Published in:

Cell & Tissue Research, 2016, v. 366, n. 1, p. 163, doi. 10.1007/s00441-016-2423-9

By:

Richter, Katharina;
Rolke, Daniel;
Blenau, Wolfgang;
Baumann, Otto

Publication type:

Article

Characterization of a 65 kDa NIF in the nuclear matrix of the monocot Allium cepa that interacts with nuclear spectrin-like proteins.

Published in:

Cell Biology International, 2012, v. 36, n. 12, p. 1097, doi. 10.1042/CBI20120237

By:

Pérez-Munive, Clara;
Blumenthal, Sonal S. D.;
Espina, Susana Moreno Díaz

Publication type:

Article

The role of spectrin breakdown products in patients with traumatic brain injury: a systematic review and meta-analysis.

Published in:

Neurological Sciences, 2023, v. 44, n. 4, p. 1171, doi. 10.1007/s10072-022-06558-y

By:

Liu, Yang;
Yao, Xiaomeng;
Lv, Xianglin;
Qian, Jinghua

Publication type:

Article

Ischemic preconditioning attenuates of ischemia-induced degradation of spectrin and tau: implications for ischemic tolerance.

Published in:

Neurological Sciences, 2011, v. 32, n. 2, p. 229, doi. 10.1007/s10072-010-0359-5

By:

Nakajima, Takayuki;
Ochi, Syoichi;
Oda, Chika;
Ishii, Maki;
Ogawa, Kazushige

Publication type:

Article

Genetic predisposition which regulates the spectrin content of bovine red cell membrane: Focal structural alteration of a -spectrin generated by polymorphism of the spectrin genes.

Published in:

Japanese Journal of Veterinary Research, 2012, v. 60, n. 2/3, p. 173

By:

Kizaki, Kota

Publication type:

Article

Role of α-II-spectrin breakdown products in the prediction of the severity and clinical outcome of acute traumatic brain injury.

Published in:

Experimental & Therapeutic Medicine, 2016, v. 11, n. 5, p. 2049, doi. 10.3892/etm.2016.3153

By:

SHANGYU CHEN;
QIANKUN SHI;
SHUYUN ZHENG;
LIANGSHEN LUO;
SHOUTAO YUAN;
XIANG WANG;
ZIHAO CHENG;
WENHAO ZHANG

Publication type:

Article

Comparison of prognoses according to non-positive and positive spectrin αII expression detected immunohistochemically in epithelial ovarian carcinoma: a retrospective study.

Published in:

Cancer Medicine, 2016, v. 5, n. 6, p. 1081, doi. 10.1002/cam4.683

By:

Maeda, Osamu;
Miyata ‐ Takata, Tomoko;
Shibata, Kiyosumi;
Kajiyama, Hiroaki;
Mizuno, Mika;
Tamakoshi, Koji;
Shimoyama, Yoshie;
Nakamura, Shigeo;
Kikkawa, Fumitaka

Publication type:

Article

Mechanical characterization of spectrin at the molecular level.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-67500-0

By:

Hossain, Md Nahian Bin;
Adnan, Ashfaq

Publication type:

Article

Role of Spectrin in Endocytosis.

Published in:

Cells (2073-4409), 2022, v. 11, n. 15, p. 2459, doi. 10.3390/cells11152459

By:

Li, Donghai

Publication type:

Article

Actomyosin Contractility in the Generation and Plasticity of Axons and Dendritic Spines.

Published in:

Cells (2073-4409), 2020, v. 9, n. 9, p. 2006, doi. 10.3390/cells9092006

By:

Mikhaylova, Marina;
Rentsch, Jakob;
Ewers, Helge

Publication type:

Article

SPTAN1 encephalopathy: distinct phenotypes and genotypes.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 4, p. 167, doi. 10.1038/jhg.2015.5

By:

Tohyama, Jun;
Nakashima, Mitsuko;
Nabatame, Shin;
Gaik-Siew, Ch'ng;
Miyata, Rie;
Rener-Primec, Zvonka;
Kato, Mitsuhiro;
Matsumoto, Naomichi;
Saitsu, Hirotomo

Publication type:

Article

A Japanese SCA5 family with a novel three-nucleotide in-frame deletion mutation in the SPTBN2 gene: a clinical and genetic study.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 10, p. 569, doi. 10.1038/jhg.2014.74

By:

Wang, Ying;
Koh, Kishin;
Miwa, Michiaki;
Yamashiro, Nobuo;
Shindo, Kazumasa;
Takiyama, Yoshihisa

Publication type:

Article

Robust adaptive optics for localization microscopy deep in complex tissue.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23647-2

By:

Siemons, Marijn E.;
Hanemaaijer, Naomi A. K.;
Kole, Maarten H. P.;
Kapitein, Lukas C.

Publication type:

Article

Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia.

Published in:

Clinical Genetics, 2019, v. 96, n. 2, p. 169, doi. 10.1111/cge.13562

By:

Nicita, Francesco;
Nardella, Marta;
Bellacchio, Emanuele;
Alfieri, Paolo;
Terrone, Gaetano;
Piccini, Giorgia;
Graziola, Federica;
Pignata, Claudio;
Capuano, Alessandro;
Bertini, Enrico;
Zanni, Ginevra

Publication type:

Article

Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophy.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 7, p. 796, doi. 10.1038/ejhg.2011.271

By:

Hamdan, Fadi F;
Saitsu, Hirotomo;
Nishiyama, Kiyomi;
Gauthier, Julie;
Dobrzeniecka, Sylvia;
Spiegelman, Dan;
Lacaille, Jean-Claude;
Décarie, Jean-Claude;
Matsumoto, Naomichi;
Rouleau, Guy A;
Michaud, Jacques L

Publication type:

Article