114 related articles for article (PubMed ID: 11566270)
1. Genomic organization of the human COL3A1 and COL5A2 genes: COL5A2 has evolved differently than the other minor fibrillar collagen genes.
Välkkilä M; Melkoniemi M; Kvist L; Kuivaniemi H; Tromp G; Ala-Kokko L
Matrix Biol; 2001 Sep; 20(5-6):357-66. PubMed ID: 11566270
[TBL] [Abstract][Full Text] [Related]
2. The human COL11A2 gene structure indicates that the gene has not evolved with the genes for the major fibrillar collagens.
Vuristo MM; Pihlajamaa T; Vandenberg P; Prockop DJ; Ala-Kokko L
J Biol Chem; 1995 Sep; 270(39):22873-81. PubMed ID: 7559422
[TBL] [Abstract][Full Text] [Related]
3. Complete structural organization of the human alpha 1 (V) collagen gene (COL5A1): divergence from the conserved organization of other characterized fibrillar collagen genes.
Takahara K; Hoffman GG; Greenspan DS
Genomics; 1995 Oct; 29(3):588-97. PubMed ID: 8575750
[TBL] [Abstract][Full Text] [Related]
4. Homozygosity and Heterozygosity for Null Col5a2 Alleles Produce Embryonic Lethality and a Novel Classic Ehlers-Danlos Syndrome-Related Phenotype.
Park AC; Phillips CL; Pfeiffer FM; Roenneburg DA; Kernien JF; Adams SM; Davidson JM; Birk DE; Greenspan DS
Am J Pathol; 2015 Jul; 185(7):2000-11. PubMed ID: 25987251
[TBL] [Abstract][Full Text] [Related]
5. An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome.
Nicholls AC; Oliver JE; McCarron S; Harrison JB; Greenspan DS; Pope FM
J Med Genet; 1996 Nov; 33(11):940-6. PubMed ID: 8950675
[TBL] [Abstract][Full Text] [Related]
6. Organization of the exons coding for pro alpha 1(II) collagen N-propeptide confirms a distinct evolutionary history of this domain of the fibrillar collagen genes.
Su MW; Benson-Chanda V; Vissing H; Ramirez F
Genomics; 1989 Apr; 4(3):438-41. PubMed ID: 2714801
[TBL] [Abstract][Full Text] [Related]
7. The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization.
Kimura T; Cheah KS; Chan SD; Lui VC; Mattei MG; van der Rest M; Ono K; Solomon E; Ninomiya Y; Olsen BR
J Biol Chem; 1989 Aug; 264(23):13910-6. PubMed ID: 2760050
[TBL] [Abstract][Full Text] [Related]
8. The pro alpha 2(V) collagen gene is evolutionarily related to the major fibrillar-forming collagens.
Weil D; Bernard M; Gargano S; Ramirez F
Nucleic Acids Res; 1987 Jan; 15(1):181-98. PubMed ID: 3029669
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations.
Ritelli M; Dordoni C; Venturini M; Chiarelli N; Quinzani S; Traversa M; Zoppi N; Vascellaro A; Wischmeijer A; Manfredini E; Garavelli L; Calzavara-Pinton P; Colombi M
Orphanet J Rare Dis; 2013 Apr; 8():58. PubMed ID: 23587214
[TBL] [Abstract][Full Text] [Related]
10. Characterization of a fibrillar collagen gene in sponges reveals the early evolutionary appearance of two collagen gene families.
Exposito JY; Garrone R
Proc Natl Acad Sci U S A; 1990 Sep; 87(17):6669-73. PubMed ID: 2395869
[TBL] [Abstract][Full Text] [Related]
11. Genetic distance of two fibrillar collagen loci, COL3A1 and COL5A2, located on the long arm of human chromosome 2.
Tsipouras P; Schwartz RC; Liddell AC; Salkeld CS; Weil D; Ramirez F
Genomics; 1988 Oct; 3(3):275-7. PubMed ID: 3224983
[TBL] [Abstract][Full Text] [Related]
12. Linkage mapping of the gene for type III collagen (COL3A1) to human chromosome 2q using a VNTR polymorphism.
Tiller GE; Polumbo PA; Summar ML
Genomics; 1994 Mar; 20(2):275-7. PubMed ID: 8020975
[TBL] [Abstract][Full Text] [Related]
13. Characterization of 64-, 123- and 182-base-pair exons in the mouse alpha 2(IV) collagen gene.
Kurkinen M; Bernard MP; Barlow DP; Chow LT
Nature; 1985 Sep 12-18; 317(6033):177-9. PubMed ID: 3839908
[TBL] [Abstract][Full Text] [Related]
14. Alpha 1 type IV collagen gene evolved differently from fibrillar collagen genes.
Sakurai Y; Sullivan M; Yamada Y
J Biol Chem; 1986 May; 261(15):6654-7. PubMed ID: 3009468
[TBL] [Abstract][Full Text] [Related]
15. Evolution of collagen IV genes from a 54-base pair exon: a role for introns in gene evolution.
Butticè G; Kaytes P; D'Armiento J; Vogeli G; Kurkinen M
J Mol Evol; 1990 Jun; 30(6):479-88. PubMed ID: 2115927
[TBL] [Abstract][Full Text] [Related]
16. Cloning of an annelid fibrillar-collagen gene and phylogenetic analysis of vertebrate and invertebrate collagens.
Sicot FX; Exposito JY; Masselot M; Garrone R; Deutsch J; Gaill F
Eur J Biochem; 1997 May; 246(1):50-8. PubMed ID: 9210465
[TBL] [Abstract][Full Text] [Related]
17. Extracellular matrix containing mutated fibrillin-1 (Fbn1) down regulates Col1a1, Col1a2, Col3a1, Col5a1, and Col5a2 mRNA levels in Tsk/+ and Tsk/Tsk embryonic fibroblasts.
Christner PJ; Ayitey S
Amino Acids; 2006 Jun; 30(4):445-51. PubMed ID: 16583319
[TBL] [Abstract][Full Text] [Related]
18. Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency.
Meienberg J; Rohrbach M; Neuenschwander S; Spanaus K; Giunta C; Alonso S; Arnold E; Henggeler C; Regenass S; Patrignani A; Azzarello-Burri S; Steiner B; Nygren AO; Carrel T; Steinmann B; Mátyás G
Eur J Hum Genet; 2010 Dec; 18(12):1315-21. PubMed ID: 20648054
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of a patient with classical Ehlers-Danlos syndrome due to a 9q34 duplication affecting COL5A1.
Kuroda Y; Ohashi I; Naruto T; Ida K; Enomoto Y; Saito T; Nagai JI; Kurosawa K
Congenit Anom (Kyoto); 2018 Nov; 58(6):191-193. PubMed ID: 29520887
[TBL] [Abstract][Full Text] [Related]
20. A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II.
Richards AJ; Martin S; Nicholls AC; Harrison JB; Pope FM; Burrows NP
J Med Genet; 1998 Oct; 35(10):846-8. PubMed ID: 9783710
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]