87 related articles for article (PubMed ID: 9735344)
1. Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutation.
Durkin ME; Albrechtsen R; Chambers DM; Abbott CM; Wewer UM
Biochem Biophys Res Commun; 1998 Sep; 250(1):125-30. PubMed ID: 9735344
[TBL] [Abstract][Full Text] [Related]
2. Linkage mapping around the ragged (Ra) and wasted (wst) loci on distal mouse chromosome 2.
Abbott C; Malas S; Pilz A; Pate L; Ali R; Peters J
Genomics; 1994 Mar; 20(1):94-8. PubMed ID: 8020960
[TBL] [Abstract][Full Text] [Related]
3. Tissue-specific expression of the human laminin alpha5-chain, and mapping of the gene to human chromosome 20q13.2-13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutation.
Durkin ME; Loechel F; Mattei MG; Gilpin BJ; Albrechtsen R; Wewer UM
FEBS Lett; 1997 Jul; 411(2-3):296-300. PubMed ID: 9271224
[TBL] [Abstract][Full Text] [Related]
4. Epithelial laminin alpha5 is necessary for distal epithelial cell maturation, VEGF production, and alveolization in the developing murine lung.
Nguyen NM; Kelley DG; Schlueter JA; Meyer MJ; Senior RM; Miner JH
Dev Biol; 2005 Jun; 282(1):111-25. PubMed ID: 15936333
[TBL] [Abstract][Full Text] [Related]
5. Defective glomerulogenesis in the absence of laminin alpha5 demonstrates a developmental role for the kidney glomerular basement membrane.
Miner JH; Li C
Dev Biol; 2000 Jan; 217(2):278-89. PubMed ID: 10625553
[TBL] [Abstract][Full Text] [Related]
6. A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice.
Clark RM; Marker PC; Kingsley DM
Genomics; 2000 Jul; 67(1):19-27. PubMed ID: 10945466
[TBL] [Abstract][Full Text] [Related]
7. Laminin alpha5 is essential for the formation of the zebrafish fins.
Webb AE; Sanderford J; Frank D; Talbot WS; Driever W; Kimelman D
Dev Biol; 2007 Nov; 311(2):369-82. PubMed ID: 17919534
[TBL] [Abstract][Full Text] [Related]
8. Analysis of the Pax-3 gene in the mouse mutant splotch.
Goulding M; Sterrer S; Fleming J; Balling R; Nadeau J; Moore KJ; Brown SD; Steel KP; Gruss P
Genomics; 1993 Aug; 17(2):355-63. PubMed ID: 8406486
[TBL] [Abstract][Full Text] [Related]
9. The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene.
Suzuki T; Li W; Zhang Q; Novak EK; Sviderskaya EV; Wilson A; Bennett DC; Roe BA; Swank RT; Spritz RA
Genomics; 2001 Nov; 78(1-2):30-7. PubMed ID: 11707070
[TBL] [Abstract][Full Text] [Related]
10. Transgenic expression of human LAMA5 suppresses murine Lama5 mRNA and laminin α5 protein deposition.
Steenhard BM; Zelenchuk A; Stroganova L; Isom K; St John PL; Andrews GK; Peterson KR; Abrahamson DR
PLoS One; 2011; 6(9):e23926. PubMed ID: 21915268
[TBL] [Abstract][Full Text] [Related]
11. Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
Graw J; Löster J; Soewarto D; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1574-80. PubMed ID: 11381063
[TBL] [Abstract][Full Text] [Related]
12. High-resolution mapping of the Gli3 deletion in the mouse extra-toesH mutant.
Genestine M; Robert B; Lallemand Y
Genesis; 2007 Mar; 45(3):107-12. PubMed ID: 17304534
[TBL] [Abstract][Full Text] [Related]
13. S-laminin: mapping to mouse chromosome 9 and expression in the linked mutants tippy and ducky.
Porter BE; Justice MJ; Copeland NG; Jenkins NA; Hunter DD; Merlie JP; Sanes JR
Genomics; 1993 Apr; 16(1):278-81. PubMed ID: 8486374
[TBL] [Abstract][Full Text] [Related]
14. Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.
Graw J; Jung M; Löster J; Klopp N; Soewarto D; Fella C; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Genomics; 1999 Nov; 62(1):67-73. PubMed ID: 10585769
[TBL] [Abstract][Full Text] [Related]
15. Molecular dissection of laminin alpha 5 in vivo reveals separable domain-specific roles in embryonic development and kidney function.
Kikkawa Y; Miner JH
Dev Biol; 2006 Aug; 296(1):265-77. PubMed ID: 16750824
[TBL] [Abstract][Full Text] [Related]
16. Laminin alpha 5 is required for lobar septation and visceral pleural basement membrane formation in the developing mouse lung.
Nguyen NM; Miner JH; Pierce RA; Senior RM
Dev Biol; 2002 Jun; 246(2):231-44. PubMed ID: 12051813
[TBL] [Abstract][Full Text] [Related]
17. Requirement for basement membrane laminin α5 during urethral and external genital development.
Lin C; Werner R; Ma L; Miner JH
Mech Dev; 2016 Aug; 141():62-69. PubMed ID: 27208857
[TBL] [Abstract][Full Text] [Related]
18. Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice.
Pennisi D; Gardner J; Chambers D; Hosking B; Peters J; Muscat G; Abbott C; Koopman P
Nat Genet; 2000 Apr; 24(4):434-7. PubMed ID: 10742113
[TBL] [Abstract][Full Text] [Related]
19. Laminin compensation in collagen alpha3(IV) knockout (Alport) glomeruli contributes to permeability defects.
Abrahamson DR; Isom K; Roach E; Stroganova L; Zelenchuk A; Miner JH; St John PL
J Am Soc Nephrol; 2007 Sep; 18(9):2465-72. PubMed ID: 17699809
[TBL] [Abstract][Full Text] [Related]
20. A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Puk O; Esposito I; Söker T; Löster J; Budde B; Nürnberg P; Michel-Soewarto D; Fuchs H; Wolf E; Hrabé de Angelis M; Graw J
Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4311-8. PubMed ID: 19407009
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
