These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
101 related articles for article (PubMed ID: 16963222)
1. Defective splicing of Megf7/Lrp4, a regulator of distal limb development, in autosomal recessive mulefoot disease. Johnson EB; Steffen DJ; Lynch KW; Herz J Genomics; 2006 Nov; 88(5):600-9. PubMed ID: 16963222 [TBL] [Abstract][Full Text] [Related]
2. Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle. Duchesne A; Gautier M; Chadi S; Grohs C; Floriot S; Gallard Y; Caste G; Ducos A; Eggen A Genomics; 2006 Nov; 88(5):610-21. PubMed ID: 16859890 [TBL] [Abstract][Full Text] [Related]
3. Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4). Drögemüller C; Leeb T; Harlizius B; Tammen I; Distl O; Höltershinken M; Gentile A; Duchesne A; Eggen A BMC Genet; 2007 Feb; 8():5. PubMed ID: 17319939 [TBL] [Abstract][Full Text] [Related]
4. Abnormal development of the apical ectodermal ridge and polysyndactyly in Megf7-deficient mice. Johnson EB; Hammer RE; Herz J Hum Mol Genet; 2005 Nov; 14(22):3523-38. PubMed ID: 16207730 [TBL] [Abstract][Full Text] [Related]
5. Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse. Simon-Chazottes D; Tutois S; Kuehn M; Evans M; Bourgade F; Cook S; Davisson MT; Guénet JL Genomics; 2006 May; 87(5):673-7. PubMed ID: 16517118 [TBL] [Abstract][Full Text] [Related]
6. Genetic analysis of syndactyly in German Holstein cattle. Drögemüller C; Distl O Vet J; 2006 Jan; 171(1):120-5. PubMed ID: 16427589 [TBL] [Abstract][Full Text] [Related]
7. The bovine aristaless-like homeobox 4 (ALX4) as a candidate gene for syndactyly. Wöhlke A; Kuiper H; Distl O; Drögemüller C Cytogenet Genome Res; 2006; 115(2):123-8. PubMed ID: 17065792 [TBL] [Abstract][Full Text] [Related]
8. Identity-by-descent mapping of recessive traits in livestock: application to map the bovine syndactyly locus to chromosome 15. Charlier C; Farnir F; Berzi P; Vanmanshoven P; Brouwers B; Vromans H; Georges M Genome Res; 1996 Jul; 6(7):580-9. PubMed ID: 8796345 [TBL] [Abstract][Full Text] [Related]
9. [Case report: Syndactyly in German Holstein calves]. Bähr C; Drögemüller C; Distl O Dtsch Tierarztl Wochenschr; 2004 Dec; 111(12):473-6. PubMed ID: 15648617 [TBL] [Abstract][Full Text] [Related]
10. Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani-Lenz syndrome. Lindy AS; Bupp CP; McGee SJ; Steed E; Stevenson RE; Basehore MJ; Friez MJ Am J Med Genet A; 2014 Sep; 164A(9):2391-7. PubMed ID: 24924585 [TBL] [Abstract][Full Text] [Related]
11. Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review. Whyte MP; Deepak Amalnath S; McAlister WH; Pedapati R; Muthupillai V; Duan S; Huskey M; Bijanki VN; Mumm S Bone; 2018 Nov; 116():321-332. PubMed ID: 30077757 [TBL] [Abstract][Full Text] [Related]
12. Cenani-Lenz syndrome restricted to limb and kidney anomalies associated with a novel LRP4 missense mutation. Khan TN; Klar J; Ali Z; Khan F; Baig SM; Dahl N Eur J Med Genet; 2013 Jul; 56(7):371-4. PubMed ID: 23664847 [TBL] [Abstract][Full Text] [Related]
13. The previously reported LRP4 c.4940C>T variant is not associated with syndactyly in cattle. Eager KLM; Cauchi M; Willet CE; Häfliger IM; Drögemüller C; O'Rourke BA; Tammen I Anim Genet; 2021 Jun; 52(3):380-381. PubMed ID: 33751600 [No Abstract] [Full Text] [Related]
14. A novel biallelic splice-site variant in the LRP4 gene causes sclerosteosis 2. Bukowska-Olech E; Sowińska-Seidler A; Szczałuba K; Jamsheer A Birth Defects Res; 2020 May; 112(9):652-659. PubMed ID: 32286743 [TBL] [Abstract][Full Text] [Related]
15. The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans. Boudin E; Yorgan T; Fijalkowski I; Sonntag S; Steenackers E; Hendrickx G; Peeters S; De Maré A; Vervaet B; Verhulst A; Mortier G; D'Haese P; Schinke T; Van Hul W J Bone Miner Res; 2017 Aug; 32(8):1739-1749. PubMed ID: 28477420 [TBL] [Abstract][Full Text] [Related]
16. LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndrome. Li Y; Pawlik B; Elcioglu N; Aglan M; Kayserili H; Yigit G; Percin F; Goodman F; Nürnberg G; Cenani A; Urquhart J; Chung BD; Ismail S; Amr K; Aslanger AD; Becker C; Netzer C; Scambler P; Eyaid W; Hamamy H; Clayton-Smith J; Hennekam R; Nürnberg P; Herz J; Temtamy SA; Wollnik B Am J Hum Genet; 2010 May; 86(5):696-706. PubMed ID: 20381006 [TBL] [Abstract][Full Text] [Related]
17. Novel splice mutation in LRP4 causes severe type of Cenani-Lenz syndactyly syndrome with oro-facial and skeletal symptoms. Afzal M; Zaman Q; Kornak U; Mundlos S; Malik S; Flöttmann R Eur J Med Genet; 2017 Aug; 60(8):421-425. PubMed ID: 28559208 [TBL] [Abstract][Full Text] [Related]
18. Novel variants in the LRP4 underlying Cenani-Lenz Syndactyly syndrome. Khan H; Chong AEQ; Bilal M; Nawaz S; Abdullah ; Abbasi S; Hussain A; Hussain S; Ullah I; Ali H; Xue S; Ahmad W J Hum Genet; 2022 May; 67(5):253-259. PubMed ID: 34857885 [TBL] [Abstract][Full Text] [Related]
19. Positional cloning of the gene LIMBIN responsible for bovine chondrodysplastic dwarfism. Takeda H; Takami M; Oguni T; Tsuji T; Yoneda K; Sato H; Ihara N; Itoh T; Kata SR; Mishina Y; Womack JE; Moritomo Y; Sugimoto Y; Kunieda T Proc Natl Acad Sci U S A; 2002 Aug; 99(16):10549-54. PubMed ID: 12136126 [TBL] [Abstract][Full Text] [Related]
20. A single point mutation in the splice donor site of the low-density-lipoprotein-receptor gene produces intron read-through, exon-skipped and cryptic-site-utilized transcripts. Maruyama T; Miyake Y; Tajima S; Funahashi T; Matsuzawa Y; Yamamoto A Eur J Biochem; 1995 Sep; 232(3):700-5. PubMed ID: 7588706 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]