Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 2
1983 2
1984 1
1985 2
1986 1
1987 3
1988 1
1989 1
1990 1
1991 4
1992 3
1993 7
1994 6
1995 2
1996 20
1997 15
1998 23
1999 34
2000 19
2001 19
2002 25
2003 32
2004 24
2005 20
2006 13
2007 20
2008 23
2009 27
2010 36
2011 34
2012 25
2013 31
2014 25
2015 41
2016 29
2017 28
2018 32
2019 28
2020 26
2021 30
2022 38
2023 27
2024 14

Text availability

Article attribute

Article type

Publication date

Search Results

708 results

Results by year

Filters applied: . Clear all
Page 1
Plectin.
Prechova M, Korelova K, Gregor M. Prechova M, et al. Curr Biol. 2023 Feb 27;33(4):R128-R130. doi: 10.1016/j.cub.2022.12.061. Curr Biol. 2023. PMID: 36854266 Free article.
Prechova et al. introduce the giant cytoskeletal crosslinker protein plectin....
Prechova et al. introduce the giant cytoskeletal crosslinker protein plectin....
Muscle-Related Plectinopathies.
Zrelski MM, Kustermann M, Winter L. Zrelski MM, et al. Cells. 2021 Sep 19;10(9):2480. doi: 10.3390/cells10092480. Cells. 2021. PMID: 34572129 Free PMC article. Review.
Plectin is a giant cytoskeletal crosslinker and intermediate filament stabilizing protein. ...We also summarize a variety of genetically manipulated mouse and cell models, which are either plectin-deficient or that specifically lack a skeletal muscle-expressed pl …
Plectin is a giant cytoskeletal crosslinker and intermediate filament stabilizing protein. ...We also summarize a variety of genetica …
Plectin in Health and Disease.
Wiche G. Wiche G. Cells. 2022 Apr 21;11(9):1412. doi: 10.3390/cells11091412. Cells. 2022. PMID: 35563718 Free PMC article.
In light of recent progress in defining a unifying mechanism for the versatile functions and disease involvement of the cytolinker protein plectin, a series of invited review articles, together with an original research article, were published in Cells as a Special Issue e …
In light of recent progress in defining a unifying mechanism for the versatile functions and disease involvement of the cytolinker protein …
MicroRNA-485-5p targets keratin 17 to regulate oral cancer stemness and chemoresistance via the integrin/FAK/Src/ERK/β-catenin pathway.
Jang TH, Huang WC, Tung SL, Lin SC, Chen PM, Cho CY, Yang YY, Yen TC, Lo GH, Chuang SE, Wang LH. Jang TH, et al. J Biomed Sci. 2022 Jun 15;29(1):42. doi: 10.1186/s12929-022-00824-z. J Biomed Sci. 2022. PMID: 35706019 Free PMC article.
Duolink proximity ligation assay (PLA) was used to examine molecular proximity between KRT17 and plectin, which is a large protein that binds cytoskeleton components. ...We identified a novel signaling cascade orchestrated by KRT17 where its association with plectin …
Duolink proximity ligation assay (PLA) was used to examine molecular proximity between KRT17 and plectin, which is a large protein th …
Plectin-related skin diseases.
Natsuga K. Natsuga K. J Dermatol Sci. 2015 Mar;77(3):139-45. doi: 10.1016/j.jdermsci.2014.11.005. Epub 2014 Nov 28. J Dermatol Sci. 2015. PMID: 25530118 Review.
In addition, a point mutation in the rod domain of plectin leads to autosomal dominant EBS, called as EBS-Ogna. Plectin can be targeted by circulating autoantibodies in subepidermal autoimmune blistering diseases. This review summarizes plectin-related skin d …
In addition, a point mutation in the rod domain of plectin leads to autosomal dominant EBS, called as EBS-Ogna. Plectin can be …
Plectin in Skin Fragility Disorders.
Kiritsi D, Tsakiris L, Schauer F. Kiritsi D, et al. Cells. 2021 Oct 14;10(10):2738. doi: 10.3390/cells10102738. Cells. 2021. PMID: 34685719 Free PMC article. Review.
Skin fragility may occur through the presence of mutations in the gene encoding for plectin, PLEC, or through the presence of autoantibodies against the molecule. Below, we review the cutaneous manifestations of plectinopathies as well as their systemic involvement in spec …
Skin fragility may occur through the presence of mutations in the gene encoding for plectin, PLEC, or through the presence of autoant …
Intermediate filaments and cellular mechanics.
Goldmann WH. Goldmann WH. Cell Biol Int. 2018 Feb;42(2):132-138. doi: 10.1002/cbin.10879. Epub 2018 Jan 10. Cell Biol Int. 2018. PMID: 28980752 Review.
They crosslink each other as well as with actin filaments and microtubules by proteins, which include desmin, filamin C, plectin, and lamin (A/C). Mutations in these proteins can lead to a wide range of pathologies, some of which exhibit mechanical failure of the skin, ske …
They crosslink each other as well as with actin filaments and microtubules by proteins, which include desmin, filamin C, plectin, and …
Plectin-Mediated Intermediate Filament Functions: Why Isoforms Matter.
Wiche G. Wiche G. Cells. 2021 Aug 21;10(8):2154. doi: 10.3390/cells10082154. Cells. 2021. PMID: 34440923 Free PMC article. Review.
It is based on previous studies that provided comprehensive evidence for a concept where plectin acts as an IF recruiter, and plectin-mediated IF networking and anchoring are key elements in IF function execution. Here, plectin's global role as modulat …
It is based on previous studies that provided comprehensive evidence for a concept where plectin acts as an IF recruiter, and plec …
Biomechanical characterization of myofibrillar myopathies.
Winter L, Goldmann WH. Winter L, et al. Cell Biol Int. 2015 Apr;39(4):361-3. doi: 10.1002/cbin.10384. Epub 2014 Dec 3. Cell Biol Int. 2015. PMID: 25264173 Review.
Most MFMs are caused by mutations in genes encoding desmin, plectin, VCP, filamin C, BAG3, FHL-1, alphaB-crystallin, DNAJB6, myotilin, and ZASP. Biomechanical studies on primary human myoblasts carrying desmin and plectin mutations showed increased stiffness and red …
Most MFMs are caused by mutations in genes encoding desmin, plectin, VCP, filamin C, BAG3, FHL-1, alphaB-crystallin, DNAJB6, myotilin …
708 results