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

Year Number of Results
1984 1
1985 1
1990 1
1998 3
1999 3
2000 2
2001 3
2002 5
2003 2
2005 5
2006 4
2007 3
2008 4
2009 4
2010 2
2011 2
2012 4
2013 3
2014 4
2015 4
2016 1
2017 1
2018 1
2019 5
2020 1
2022 0
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64 results
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Page 1
Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging.
Penumatsa KC, Falcão-Pires I, Leite S, Leite-Moreira A, Bhedi CD, Nasirova S, Ma J, Sutliff RL, Fanburg BL. Penumatsa KC, et al. Front Physiol. 2020 Sep 15;11:560019. doi: 10.3389/fphys.2020.560019. eCollection 2020. Front Physiol. 2020. PMID: 33041859 Free PMC article.
., increased organ tissue stiffness) are known features of obesity and the metabolic syndrome. Similarly, cardiac diastolic dysfunction is associated with aging. ...With these observations in mind we hypothesized that TG2 may be elevated in tissues of a rat model of obesit …
., increased organ tissue stiffness) are known features of obesity and the metabolic syndrome. Similarly, cardiac diastolic dysfuncti …
Transglutaminase diseases: from biochemistry to the bedside.
Lorand L, Iismaa SE. Lorand L, et al. FASEB J. 2019 Jan;33(1):3-12. doi: 10.1096/fj.201801544R. FASEB J. 2019. PMID: 30593123
Loss of TG function is associated with numerous orphan diseases that affect a relatively small number of individuals: loss of FXIIIa (transamidase-activated form) crosslinking leads to defects in blood coagulation in FXIII deficiency; loss of TG1 and TG5 cross linking leads to de …
Loss of TG function is associated with numerous orphan diseases that affect a relatively small number of individuals: loss of FXIIIa (transa …
Autoantibodies to tissue transglutaminase in Sjögren's syndrome and related rheumatic diseases.
Luft LM, Barr SG, Martin LO, Chan EK, Fritzler MJ. Luft LM, et al. J Rheumatol. 2003 Dec;30(12):2613-9. J Rheumatol. 2003. PMID: 14719202
OBJECTIVE: Sjogren's syndrome (SS) has been reported in up to 15% of patients with biopsy proven celiac disease (CD). ...
OBJECTIVE: Sjogren's syndrome (SS) has been reported in up to 15% of patients with biopsy proven celiac disease (CD). ...
"Tissue" transglutaminase in AIDS.
Amendola A, Fesus L, Piacentini M, Szondy Z. Amendola A, et al. J Immunol Methods. 2002 Jul 1;265(1-2):145-59. doi: 10.1016/s0022-1759(02)00077-7. J Immunol Methods. 2002. PMID: 12072185 Review.
Several independent laboratories have identified "tissue" transglutaminase (tTG) as a potentially important player of the cell death program(s). This gene is specifically expressed in cells dying during mammalian development as well as in those undergoing apoptosis in vari …
Several independent laboratories have identified "tissue" transglutaminase (tTG) as a potentially important player of the cell death program …
Antitissue transglutaminase and antithyroid autoantibodies in children with Down syndrome and celiac disease.
Hansson T, Dahlbom I, Rogberg S, Nyberg BI, Dahlström J, Annerén G, Klareskog L, Dannaeus A. Hansson T, et al. J Pediatr Gastroenterol Nutr. 2005 Feb;40(2):170-4; discussion 125-7. doi: 10.1097/00005176-200502000-00016. J Pediatr Gastroenterol Nutr. 2005. PMID: 15699691
Of the 72 Down syndrome children, 11 under-went a small intestinal biopsy. RESULTS: Four of 72 children with Down syndrome were diagnosed as having CD and three of them had serum levels of immunoglobulin A tTG antibodies greater than 6 U/mL (668, 147 and 7 U/mL). On …
Of the 72 Down syndrome children, 11 under-went a small intestinal biopsy. RESULTS: Four of 72 children with Down syndrome wer …
Type 2 transglutaminase in neurodegenerative diseases: the mitochondrial connection.
Malorni W, Farrace MG, Rodolfo C, Piacentini M. Malorni W, et al. Curr Pharm Des. 2008;14(3):278-88. Curr Pharm Des. 2008. PMID: 18220838 Review.
Multiple lines of evidence suggest an involvement of the enzyme in neurodegenerative diseases, such as Huntington's (HD) and Parkinson (PD), and that its inhibition, either via drug treatments or genetic approaches, might be beneficial for the treatment of these syndrom
Multiple lines of evidence suggest an involvement of the enzyme in neurodegenerative diseases, such as Huntington's (HD) and Parkinso …
LEKTI domains D6, D7 and D8+9 serve as substrates for transglutaminase 1: implications for targeted therapy of Netherton syndrome.
Wiegmann H, Valentin F, Tarinski T, Liebau E, Loser K, Traupe H, Oji V. Wiegmann H, et al. Br J Dermatol. 2019 Nov;181(5):999-1008. doi: 10.1111/bjd.17820. Epub 2019 Jun 6. Br J Dermatol. 2019. PMID: 30801672
These results impact the development of protein replacement therapy approaches for Netherton syndrome. What's already known about this topic? LEKTI and transglutaminase (TG)1 are key proteins involved in the terminal differentiation of the epidermis. Lack of LEKTI c …
These results impact the development of protein replacement therapy approaches for Netherton syndrome. What's already known ab …
A prawn transglutaminase: molecular characterization and biochemical properties.
Arockiaraj J, Gnanam AJ, Palanisamy R, Kumaresan V, Bhatt P, Thirumalai MK, Roy A, Pasupuleti M, Kasi M, Sathyamoorthi A, Arasu A. Arockiaraj J, et al. Biochimie. 2013 Dec;95(12):2354-64. doi: 10.1016/j.biochi.2013.08.029. Epub 2013 Sep 5. Biochimie. 2013. PMID: 24012776
Results of TGase mRNA relative expression in hemocyte, before and after infected with white spot syndrome baculovirus (WSBV) and Vibrio harveyi show that the gene expression initially increases up to 24 h and then it falls down. ...
Results of TGase mRNA relative expression in hemocyte, before and after infected with white spot syndrome baculovirus (WSBV) and Vibr …
Transglutaminase 2 programs differentiating acute promyelocytic leukemia cells in all-trans retinoic acid treatment to inflammatory stage through NF-κB activation.
Jambrovics K, Uray IP, Keresztessy Z, Keillor JW, Fésüs L, Balajthy Z. Jambrovics K, et al. Haematologica. 2019 Mar;104(3):505-515. doi: 10.3324/haematol.2018.192823. Epub 2018 Sep 20. Haematologica. 2019. PMID: 30237268 Free PMC article.
Differentiation syndrome (DS) is a life-threatening complication arising during retinoid treatment of acute promyelocytic leukemia (APL). ...
Differentiation syndrome (DS) is a life-threatening complication arising during retinoid treatment of acute promyelocytic leukemia (A …
Novel transglutaminase-like peptidase and C2 domains elucidate the structure, biogenesis and evolution of the ciliary compartment.
Zhang D, Aravind L. Zhang D, et al. Cell Cycle. 2012 Oct 15;11(20):3861-75. doi: 10.4161/cc.22068. Epub 2012 Sep 14. Cell Cycle. 2012. PMID: 22983010 Free PMC article.
Mutations in components of these complexes are at the heart of human ciliopathies such as Nephronophthisis (NPHP), Meckel-Gruber syndrome (MKS), Bardet-Biedl syndrome (BBS) and Joubert syndrome (JBTS). ...
Mutations in components of these complexes are at the heart of human ciliopathies such as Nephronophthisis (NPHP), Meckel-Gruber syndrome
64 results