179 related articles for article (PubMed ID: 31623094)
1. Type IV Collagen Is Essential for Proper Function of Integrin-Mediated Adhesion in
Kiss AA; Somlyai-Popovics N; Kiss M; Boldogkői Z; Csiszár K; Mink M
Int J Mol Sci; 2019 Oct; 20(20):. PubMed ID: 31623094
[TBL] [Abstract][Full Text] [Related]
2. Drosophila type IV collagen mutation associates with immune system activation and intestinal dysfunction.
Kiss M; Kiss AA; Radics M; Popovics N; Hermesz E; Csiszár K; Mink M
Matrix Biol; 2016 Jan; 49():120-131. PubMed ID: 26363084
[TBL] [Abstract][Full Text] [Related]
3. Drosophila basement membrane collagen col4a1 mutations cause severe myopathy.
Kelemen-Valkony I; Kiss M; Csiha J; Kiss A; Bircher U; Szidonya J; Maróy P; Juhász G; Komonyi O; Csiszár K; Mink M
Matrix Biol; 2012 Jan; 31(1):29-37. PubMed ID: 22037604
[TBL] [Abstract][Full Text] [Related]
4. HANAC Col4a1 Mutation in Mice Leads to Skeletal Muscle Alterations due to a Primary Vascular Defect.
Guiraud S; Migeon T; Ferry A; Chen Z; Ouchelouche S; Verpont MC; Sado Y; Allamand V; Ronco P; Plaisier E
Am J Pathol; 2017 Mar; 187(3):505-516. PubMed ID: 28056338
[TBL] [Abstract][Full Text] [Related]
5. COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans.
Labelle-Dumais C; Dilworth DJ; Harrington EP; de Leau M; Lyons D; Kabaeva Z; Manzini MC; Dobyns WB; Walsh CA; Michele DE; Gould DB
PLoS Genet; 2011 May; 7(5):e1002062. PubMed ID: 21625620
[TBL] [Abstract][Full Text] [Related]
6. 4-Hydroxy-2-nonenal Alkylated and Peroxynitrite Nitrated Proteins Localize to the Fused Mitochondria in Malpighian Epithelial Cells of Type IV Collagen
Kiss AA; Popovics N; Boldogkői Z; Csiszár K; Mink M
Biomed Res Int; 2018; 2018():3502401. PubMed ID: 29651426
[No Abstract] [Full Text] [Related]
7. Identification of fibronectin 1 as a candidate genetic modifier in a Col4a1 mutant mouse model of Gould syndrome.
Mao M; Popli T; Jeanne M; Hoff K; Sen S; Gould DB
Dis Model Mech; 2021 Apr; 14(4):. PubMed ID: 34424299
[TBL] [Abstract][Full Text] [Related]
8. COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity.
Labelle-Dumais C; Schuitema V; Hayashi G; Hoff K; Gong W; Dao DQ; Ullian EM; Oishi P; Margeta M; Gould DB
Am J Hum Genet; 2019 May; 104(5):847-860. PubMed ID: 31051113
[TBL] [Abstract][Full Text] [Related]
9. Elevated TGFβ signaling contributes to cerebral small vessel disease in mouse models of Gould syndrome.
Branyan K; Labelle-Dumais C; Wang X; Hayashi G; Lee B; Peltz Z; Gorman S; Li BQ; Mao M; Gould DB
Matrix Biol; 2023 Jan; 115():48-70. PubMed ID: 36435425
[TBL] [Abstract][Full Text] [Related]
10. Distinct functions of the laminin β LN domain and collagen IV during cardiac extracellular matrix formation and stabilization of alary muscle attachments revealed by EMS mutagenesis in Drosophila.
Hollfelder D; Frasch M; Reim I
BMC Dev Biol; 2014 Jun; 14():26. PubMed ID: 24935095
[TBL] [Abstract][Full Text] [Related]
11. Novel COL4A1 mutations associated with HANAC syndrome: a role for the triple helical CB3[IV] domain.
Plaisier E; Chen Z; Gekeler F; Benhassine S; Dahan K; Marro B; Alamowitch S; Paques M; Ronco P
Am J Med Genet A; 2010 Oct; 152A(10):2550-5. PubMed ID: 20818663
[TBL] [Abstract][Full Text] [Related]
12. Severity of arterial defects in the retina correlates with the burden of intracerebral haemorrhage in COL4A1-related stroke.
Ratelade J; Mezouar N; Domenga-Denier V; Rochey A; Plaisier E; Joutel A
J Pathol; 2018 Apr; 244(4):408-420. PubMed ID: 29266233
[TBL] [Abstract][Full Text] [Related]
13. Life-threatening muscle complications of COL4A1-related disorder.
Okano S; Shimada S; Tanaka R; Okayama A; Kajihama A; Suzuki N; Nakau K; Takahashi S; Matsumoto N; Saitsu H; Tanboon J; Nishino I; Azuma H
Brain Dev; 2020 Jan; 42(1):93-97. PubMed ID: 31540749
[TBL] [Abstract][Full Text] [Related]
14. ER stress and basement membrane defects combine to cause glomerular and tubular renal disease resulting from Col4a1 mutations in mice.
Jones FE; Bailey MA; Murray LS; Lu Y; McNeilly S; Schlötzer-Schrehardt U; Lennon R; Sado Y; Brownstein DG; Mullins JJ; Kadler KE; Van Agtmael T
Dis Model Mech; 2016 Feb; 9(2):165-76. PubMed ID: 26839400
[TBL] [Abstract][Full Text] [Related]
15. HANAC Syndrome Col4a1 Mutation Causes Neonate Glomerular Hyperpermeability and Adult Glomerulocystic Kidney Disease.
Chen Z; Migeon T; Verpont MC; Zaidan M; Sado Y; Kerjaschki D; Ronco P; Plaisier E
J Am Soc Nephrol; 2016 Apr; 27(4):1042-54. PubMed ID: 26260163
[TBL] [Abstract][Full Text] [Related]
16. Elevated TGFβ signaling contributes to ocular anterior segment dysgenesis in Col4a1 mutant mice.
Mao M; Labelle-Dumais C; Tufa SF; Keene DR; Gould DB
Matrix Biol; 2022 Jun; 110():151-173. PubMed ID: 35525525
[TBL] [Abstract][Full Text] [Related]
17. Integrin-mediated adhesion maintains sarcomeric integrity.
Perkins AD; Ellis SJ; Asghari P; Shamsian A; Moore ED; Tanentzapf G
Dev Biol; 2010 Feb; 338(1):15-27. PubMed ID: 19879257
[TBL] [Abstract][Full Text] [Related]
18. Role of COL4A1 in basement-membrane integrity and cerebral small-vessel disease. The COL4A1 stroke syndrome.
Volonghi I; Pezzini A; Del Zotto E; Giossi A; Costa P; Ferrari D; Padovani A
Curr Med Chem; 2010; 17(13):1317-24. PubMed ID: 20166936
[TBL] [Abstract][Full Text] [Related]
19. Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations.
Kuo DS; Labelle-Dumais C; Mao M; Jeanne M; Kauffman WB; Allen J; Favor J; Gould DB
Hum Mol Genet; 2014 Apr; 23(7):1709-22. PubMed ID: 24203695
[TBL] [Abstract][Full Text] [Related]
20. Human congenital myopathy actin mutants cause myopathy and alter Z-disc structure in Drosophila flight muscle.
Sevdali M; Kumar V; Peckham M; Sparrow J
Neuromuscul Disord; 2013 Mar; 23(3):243-55. PubMed ID: 23294764
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]