المؤلفون: Sidorenko, Ekaterina, Sokolova, Maria, Pennanen, Antti P., Kyheröinen, Salla, Posern, Guido, Foisner, Roland, Vartiainen, Maria K.

المساهمون: Institute of Biotechnology, UniSport, Nuclear organization by actin

مصطلحات موضوعية: SERUM RESPONSE FACTOR, NUCLEAR-ENVELOPE PROTEIN, TRANSCRIPTION FACTORS, ACTIN CYTOSKELETON, CELL-PROLIFERATION, MYOCARDIN FAMILY, GENE, SRF, LAP2-ALPHA, DIFFERENTIATION, 1182 Biochemistry, cell and molecular biology

وصف الملف: application/pdf

العلاقة: We thank Paula Maanselka for excellent assistance. Imaging was performed at Light Microscopy Unit (LMU), which is supported by Helsinki Institute for Life Science (HiLIFE) and Biocenter Finland. This work was supported by grants (to MKV) from Sigrid Juselius foundation, Academy of Finland, Jane and Aatos Erkko foundation, Finnish Cancer foundation and HiLIFE.; Sidorenko , E , Sokolova , M , Pennanen , A P , Kyheröinen , S , Posern , G , Foisner , R & Vartiainen , M K 2022 , ' Lamina-associated polypeptide 2 alpha is required for intranuclear MRTF-A activity ' , Scientific Reports , vol. 12 , no. 1 , 2306 . https://doi.org/10.1038/s41598-022-06135-5Test; ORCID: /0000-0001-5965-8518/work/130604444; ORCID: /0000-0002-2017-0475/work/130605018; 32371b92-7371-4dd9-a04c-031fad881752; http://hdl.handle.net/10138/355568Test; 000754021000010

الإتاحة: http://hdl.handle.net/10138/355568Test

المؤلفون: Swaleha Nurulla Nadaf, Rahul T Chakor, Kaumil V Kothari, Ashraf U Mannan

المصدر: Annals of Indian Academy of Neurology, Vol 23, Iss 4, Pp 539-541 (2020)

مصطلحات موضوعية: autosomal recessive cerebellar ataxia 1 ataxia, amyotrophic lateral sclerosis, motor neuron disease, spinocerebellar ataxia of recessive ataxia, synaptic nuclear envelope protein 1 ataxia, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: http://www.annalsofian.org/article.asp?issn=0972-2327;year=2020;volume=23;issue=4;spage=539;epage=541;aulast=NadafTest; https://doaj.org/toc/0972-2327Test; https://doaj.org/toc/1998-3549Test

الوصول الحر: https://doaj.org/article/2f83ef88d4ed450898924980549b278cTest

المؤلفون: Lauren Swan, John Cardinal, David Coman

المصدر: Clinics and Practice; Volume 8; Issue 3; Pages: 1071

مصطلحات موضوعية: congenital cerebellar hypoplasia, developmental delay, ataxia, spectrin repeatcontaining nuclear envelope protein 1

وصف الملف: application/pdf

العلاقة: https://dx.doi.org/10.4081/cp.2018.1071Test

الإتاحة: https://doi.org/10.4081/cp.2018.1071Test

المؤلفون: Maria Sokolova, Guido Posern, Salla Kyheröinen, Antti Pennanen, Ekaterina Sidorenko, Maria K. Vartiainen, Roland Foisner

المساهمون: Institute of Biotechnology, UniSport, Nuclear organization by actin

المصدر: Scientific Reports, Vol 12, Iss 1, Pp 1-19 (2022)

مصطلحات موضوعية: Cytoplasm, Transcription, Genetic, Science, NUCLEAR-ENVELOPE PROTEIN, CELL-PROLIFERATION, 03 medical and health sciences, Mice, LAP2-ALPHA, 0302 clinical medicine, Cell Movement, Gene expression, Coactivator, Serum response factor, Transcriptional regulation, Animals, SERUM RESPONSE FACTOR, Cytoskeleton, Transcription factor, 030304 developmental biology, MYOCARDIN FAMILY, Cell Nucleus, 0303 health sciences, Multidisciplinary, biology, Chemistry, Chromatin binding, ACTIN CYTOSKELETON, Membrane Proteins, GENE, Actins, Chromatin, Cell biology, DNA-Binding Proteins, TRANSCRIPTION FACTORS, Histone, DIFFERENTIATION, Gene Expression Regulation, biology.protein, NIH 3T3 Cells, Trans-Activators, Medicine, 1182 Biochemistry, cell and molecular biology, SRF, 030217 neurology & neurosurgery, Protein Binding

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5816ae43deb67c3bee876c6f1007f82cTest
http://hdl.handle.net/10138/355568Test

المؤلفون: Foisner, Roland, Dechat, Thomas, von Haeseler, Arndt, Skoruppa, Michael P., Rescheneder, Philipp, Gesson, Kevin

مصطلحات موضوعية: nuclear-envelope protein, embryonic stem-cells, domain organization, genome interactions, histone methylation, 2-alpha lap2-alpha, chromatin state, prelamin-a, dna, differentiation

جغرافية الموضوع: UMW:14541

وصف الملف: text/html

العلاقة: vignette : https://repositorium.meduniwien.ac.at/titlepage/urn/urn:nbn:at:at-ubmuw:3-1298/128Test; urn:nbn:at:at-ubmuw:3-1298; https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-1298Test; local:99144872283403331; system:AC15250305

الإتاحة: https://doi.org/10.1101/gr.196220.115Test
https://resolver.obvsg.at/urn:nbn:at:at-ubmuw:3-1298Test

المؤلفون: Chun-Xiao Liu, Bi-Liu Wei, Guo-Xiong Deng, Rui-Xing Yin, Yao-Zong Guan, Peng-Fei Zheng

المصدر: Journal of Cellular and Molecular Medicine

مصطلحات موضوعية: Male, 0301 basic medicine, haplotype, Linkage disequilibrium, Multifactor Dimensionality Reduction, Linkage Disequilibrium, 0302 clinical medicine, environmental factor, single nucleotide polymorphism, Risk Factors, Genotype, Aged, 80 and over, Hypertriglyceridemia, Genetics, spectrin repeat containing nuclear envelope protein 1, RNA-Binding Proteins, Middle Aged, Lipids, 030220 oncology & carcinogenesis, Molecular Medicine, Original Article, Female, KH domain containing RNA binding gene, Adult, Hypercholesterolemia, interaction, Hyperlipidemias, Nerve Tissue Proteins, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Young Adult, 03 medical and health sciences, Humans, SNP, Genetic Predisposition to Disease, Life Style, Alleles, Genetic Association Studies, Aged, hyperlipidaemia, Haplotype, Epistasis, Genetic, Original Articles, Cell Biology, Cytoskeletal Proteins, Logistic Models, 030104 developmental biology, Haplotypes, Case-Control Studies, Mutation, Gene-Environment Interaction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a3adaef289ba5c708f40d69f96e187aTest
https://doi.org/10.1111/jcmm.15239Test

المؤلفون: Lei, Kai, Zhang, Xiaochang, Ding, Xu, Guo, Xue, Chen, Muyun, Zhu, Binggen, Xu, Tian, Zhuang, Yuan, Xu, Rener, Han, Min, Olson, Eric N.

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2009 Jun . 106(25), 10207-10212.

الوصول الحر: https://www.jstor.org/stable/40483677Test

المؤلفون: Schulte-Kreutz, Thomas

مصطلحات موضوعية: P30, Strukturprotein, Kernmembran, syne-1, myne-1, structure protein, nuclear envelope protein, ddc:610

وصف الملف: application/pdf

العلاقة: http://nbn-resolving.de/urn:nbn:de:hebis:26-opus-59900Test; https://jlupub.ub.uni-giessen.de//handle/jlupub/13922Test; http://dx.doi.org/10.22029/jlupub-13304Test

الإتاحة: https://doi.org/10.22029/jlupub-13304Test
https://jlupub.ub.uni-giessen.de//handle/jlupub/13922Test
http://nbn-resolving.de/urn:nbn:de:hebis:26-opus-59900Test

المؤلفون: Kaumil V Kothari, Swaleha Nadaf, Rahul T Chakor, Ashraf U Mannan

المصدر: Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 23, Iss 4, Pp 539-541 (2020)

مصطلحات موضوعية: amyotrophic lateral sclerosis, Pathology, medicine.medical_specialty, Ataxia, synaptic nuclear envelope protein 1 ataxia, Case Report, lcsh:RC346-429, Frameshift mutation, Fasciculation, 03 medical and health sciences, 0302 clinical medicine, Atrophy, Medicine, 030212 general & internal medicine, Amyotrophic lateral sclerosis, lcsh:Neurology. Diseases of the nervous system, Cerebellar ataxia, business.industry, medicine.disease, Gene deletion mutation, Autosomal recessive cerebellar ataxia 1 ataxia, spinocerebellar ataxia of recessive ataxia, motor neuron disease, Gait Ataxia, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa667f265ff684e38e2fa5e7af63ee1bTest
https://doi.org/10.4103/aian.aian_448_18Test

المؤلفون: John Cardinal, Lauren Swan, David Coman

المصدر: Clinics and Practice
Clinics and Practice, Vol 8, Iss 3 (2018)

مصطلحات موضوعية: 0301 basic medicine, Pathology, medicine.medical_specialty, Ataxia, Developmental delay, SYNE1, Case Report, 030105 genetics & heredity, 03 medical and health sciences, Dysarthria, 0302 clinical medicine, Congenital cerebellar hypoplasia, Spectrin repeatcontaining nuclear envelope protein 1, medicine, Spectrin, lcsh:R5-920, business.industry, Autosomal recessive cerebellar ataxia, General Medicine, medicine.disease, Actin cytoskeleton, Phenotype, Spinocerebellar ataxia, medicine.symptom, Age of onset, lcsh:Medicine (General), business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d3db90c7b32fd5fceadc58da7f83312Test
https://doi.org/10.4081/cp.2018.1071Test