236 related articles for article (PubMed ID: 32430393)
1. Zebrafish models of skeletal dysplasia induced by cholesterol biosynthesis deficiency.
Anderson RA; Schwalbach KT; Mui SR; LeClair EE; Topczewska JM; Topczewski J
Dis Model Mech; 2020 Jun; 13(6):. PubMed ID: 32430393
[TBL] [Abstract][Full Text] [Related]
2.
Sun X; Zhang R; Chen H; Du X; Chen S; Huang J; Liu M; Xu M; Luo F; Jin M; Su N; Qi H; Yang J; Tan Q; Zhang D; Ni Z; Liang S; Zhang B; Chen D; Zhang X; Luo L; Chen L; Xie Y
Theranostics; 2020; 10(16):7111-7130. PubMed ID: 32641982
[TBL] [Abstract][Full Text] [Related]
3. The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis.
Melville DB; Montero-Balaguer M; Levic DS; Bradley K; Smith JR; Hatzopoulos AK; Knapik EW
Dis Model Mech; 2011 Nov; 4(6):763-76. PubMed ID: 21729877
[TBL] [Abstract][Full Text] [Related]
4. Establishment of a bone-specific col10a1:GFP transgenic zebrafish.
Kim YI; Lee S; Jung SH; Kim HT; Choi JH; Lee MS; You KH; Yeo SY; Yoo KW; Kwak S; Lee JN; Park R; Choe SK; Kim CH
Mol Cells; 2013 Aug; 36(2):145-50. PubMed ID: 23852131
[TBL] [Abstract][Full Text] [Related]
5. Zebrafish model for spondylo-megaepiphyseal-metaphyseal dysplasia reveals post-embryonic roles of Nkx3.2 in the skeleton.
Smeeton J; Natarajan N; Naveen Kumar A; Miyashita T; Baddam P; Fabian P; Graf D; Crump JG
Development; 2021 Jan; 148(2):. PubMed ID: 33462117
[TBL] [Abstract][Full Text] [Related]
6. Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway.
Quintana AM; Picchione F; Klein Geltink RI; Taylor MR; Grosveld GC
Dis Model Mech; 2014 Feb; 7(2):265-70. PubMed ID: 24357328
[TBL] [Abstract][Full Text] [Related]
7. New tools for studying osteoarthritis genetics in zebrafish.
Mitchell RE; Huitema LF; Skinner RE; Brunt LH; Severn C; Schulte-Merker S; Hammond CL
Osteoarthritis Cartilage; 2013 Feb; 21(2):269-78. PubMed ID: 23159952
[TBL] [Abstract][Full Text] [Related]
8. Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome.
Besnard T; Sloboda N; Goldenberg A; Küry S; Cogné B; Breheret F; Trochu E; Conrad S; Vincent M; Deb W; Balguerie X; Barbarot S; Baujat G; Ben-Omran T; Bursztejn AC; Carmignac V; Datta AN; Delignières A; Faivre L; Gardie B; Guéant JL; Kuentz P; Lenglet M; Nassogne MC; Ramaekers V; Schnur RE; Si Y; Torti E; Thevenon J; Vabres P; Van Maldergem L; Wand D; Wiedemann A; Cariou B; Redon R; Lamazière A; Bézieau S; Feillet F; Isidor B
Genet Med; 2019 Sep; 21(9):2025-2035. PubMed ID: 30723320
[TBL] [Abstract][Full Text] [Related]
9. Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development.
Quintana AM; Hernandez JA; Gonzalez CG
PLoS One; 2017; 12(7):e0180856. PubMed ID: 28686747
[TBL] [Abstract][Full Text] [Related]
10. Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice.
Wada Y; Kikuchi A; Kaga A; Shimizu N; Ito J; Onuma R; Fujishima F; Totsune E; Sato R; Niihori T; Shirota M; Funayama R; Sato K; Nakazawa T; Nakayama K; Aoki Y; Aiba S; Nakagawa K; Kure S
PLoS Genet; 2020 Feb; 16(2):e1008628. PubMed ID: 32101538
[TBL] [Abstract][Full Text] [Related]
11. New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform Dermatitis.
Kalay Yildizhan I; Gökpınar İli E; Onoufriadis A; Kocyigit P; Kesidou E; Simpson MA; McGrath JA; Kutlay NY; Kundakci N
Cytogenet Genome Res; 2020; 160(9):523-530. PubMed ID: 33161406
[TBL] [Abstract][Full Text] [Related]
12. Defective postnatal endochondral bone development by chondrocyte-specific targeted expression of parathyroid hormone type 2 receptor.
Panda DK; Goltzman D; Karaplis AC
Am J Physiol Endocrinol Metab; 2012 Dec; 303(12):E1489-501. PubMed ID: 23092913
[TBL] [Abstract][Full Text] [Related]
13. Cartilage ultrastructure in proteoglycan-deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders.
Wiweger MI; Avramut CM; de Andrea CE; Prins FA; Koster AJ; Ravelli RB; Hogendoorn PC
J Pathol; 2011 Mar; 223(4):531-42. PubMed ID: 21294126
[TBL] [Abstract][Full Text] [Related]
14. HEM dysplasia and ichthyosis are likely laminopathies and not due to 3beta-hydroxysterol Delta14-reductase deficiency.
Wassif CA; Brownson KE; Sterner AL; Forlino A; Zerfas PM; Wilson WK; Starost MF; Porter FD
Hum Mol Genet; 2007 May; 16(10):1176-87. PubMed ID: 17403717
[TBL] [Abstract][Full Text] [Related]
15. Radiographic analysis of zebrafish skeletal defects.
Fisher S; Jagadeeswaran P; Halpern ME
Dev Biol; 2003 Dec; 264(1):64-76. PubMed ID: 14623232
[TBL] [Abstract][Full Text] [Related]
16. NANS-mediated synthesis of sialic acid is required for brain and skeletal development.
van Karnebeek CD; Bonafé L; Wen XY; Tarailo-Graovac M; Balzano S; Royer-Bertrand B; Ashikov A; Garavelli L; Mammi I; Turolla L; Breen C; Donnai D; Cormier-Daire V; Heron D; Nishimura G; Uchikawa S; Campos-Xavier B; Rossi A; Hennet T; Brand-Arzamendi K; Rozmus J; Harshman K; Stevenson BJ; Girardi E; Superti-Furga G; Dewan T; Collingridge A; Halparin J; Ross CJ; Van Allen MI; Rossi A; Engelke UF; Kluijtmans LA; van der Heeft E; Renkema H; de Brouwer A; Huijben K; Zijlstra F; Heise T; Boltje T; Wasserman WW; Rivolta C; Unger S; Lefeber DJ; Wevers RA; Superti-Furga A
Nat Genet; 2016 Jul; 48(7):777-84. PubMed ID: 27213289
[TBL] [Abstract][Full Text] [Related]
17. Skeletal-specific expression of Fgd1 during bone formation and skeletal defects in faciogenital dysplasia (FGDY; Aarskog syndrome).
Gorski JL; Estrada L; Hu C; Liu Z
Dev Dyn; 2000 Aug; 218(4):573-86. PubMed ID: 10906777
[TBL] [Abstract][Full Text] [Related]
18. Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis.
Rossi M; Hall CM; Bouvier R; Collardeau-Frachon S; Le Breton F; Bucourt M; Cordier MP; Vianey-Saban C; Parenti G; Andria G; Le Merrer M; Edery P; Offiah AC
Pediatr Radiol; 2015 Jul; 45(7):965-76. PubMed ID: 25646736
[TBL] [Abstract][Full Text] [Related]
19. Genetic Mutations in jamb, jamc, and myomaker Revealed Different Roles on Myoblast Fusion and Muscle Growth.
Si Y; Wen H; Du S
Mar Biotechnol (NY); 2019 Feb; 21(1):111-123. PubMed ID: 30467785
[TBL] [Abstract][Full Text] [Related]
20. Characterization of two new zebrafish members of the hedgehog family: atypical expression of a zebrafish indian hedgehog gene in skeletal elements of both endochondral and dermal origins.
Avaron F; Hoffman L; Guay D; Akimenko MA
Dev Dyn; 2006 Feb; 235(2):478-89. PubMed ID: 16292774
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]