507 related articles for article (PubMed ID: 10945466)
1. 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]
2. Single nucleotide polymorphisms in the chicken Lmbr1 gene are associated with chicken polydactyly.
Huang YQ; Deng XM; Du ZQ; Qiu X; Du X; Chen W; Morisson M; Leroux S; Ponce de Léon FA; Da Y; Li N
Gene; 2006 Jun; 374():10-8. PubMed ID: 16650944
[TBL] [Abstract][Full Text] [Related]
3. The Hemimelic extra toes mouse mutant: Historical perspective on unraveling mechanisms of dysmorphogenesis.
Knudsen TB; Kochhar DM
Birth Defects Res C Embryo Today; 2010 Jun; 90(2):155-62. PubMed ID: 20544697
[TBL] [Abstract][Full Text] [Related]
4. Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly.
Lettice LA; Horikoshi T; Heaney SJ; van Baren MJ; van der Linde HC; Breedveld GJ; Joosse M; Akarsu N; Oostra BA; Endo N; Shibata M; Suzuki M; Takahashi E; Shinka T; Nakahori Y; Ayusawa D; Nakabayashi K; Scherer SW; Heutink P; Hill RE; Noji S
Proc Natl Acad Sci U S A; 2002 May; 99(11):7548-53. PubMed ID: 12032320
[TBL] [Abstract][Full Text] [Related]
5. Elimination of a long-range cis-regulatory module causes complete loss of limb-specific Shh expression and truncation of the mouse limb.
Sagai T; Hosoya M; Mizushina Y; Tamura M; Shiroishi T
Development; 2005 Feb; 132(4):797-803. PubMed ID: 15677727
[TBL] [Abstract][Full Text] [Related]
6. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
Tsukurov O; Boehmer A; Flynn J; Nicolai JP; Hamel BC; Traill S; Zaleske D; Mankin HJ; Yeon H; Ho C
Nat Genet; 1994 Mar; 6(3):282-6. PubMed ID: 8012391
[TBL] [Abstract][Full Text] [Related]
7. Homozygous feature of isolated triphalangeal thumb-preaxial polydactyly linked to 7q36: no phenotypic difference between homozygotes and heterozygotes.
Semerci CN; Demirkan F; Ozdemir M; Biskin E; Akin B; Bagci H; Akarsu NA
Clin Genet; 2009 Jul; 76(1):85-90. PubMed ID: 19519794
[TBL] [Abstract][Full Text] [Related]
8. Polydactyly in the Strong's luxoid mouse is suppressed by limb deformity alleles.
Vogt TF; Leder P
Dev Genet; 1996; 19(1):33-42. PubMed ID: 8792607
[TBL] [Abstract][Full Text] [Related]
9. Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1.
Clark RM; Marker PC; Roessler E; Dutra A; Schimenti JC; Muenke M; Kingsley DM
Genetics; 2001 Oct; 159(2):715-26. PubMed ID: 11606546
[TBL] [Abstract][Full Text] [Related]
10. Isolation of the chicken Lmbr1 coding sequence and characterization of its role during chick limb development.
Maas SA; Fallon JF
Dev Dyn; 2004 Mar; 229(3):520-8. PubMed ID: 14991708
[TBL] [Abstract][Full Text] [Related]
11. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
Mohlke KL; Purkayastha AA; Westrick RJ; Ginsburg D
Genomics; 1998 Nov; 54(1):19-30. PubMed ID: 9806826
[TBL] [Abstract][Full Text] [Related]
12. A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35.
Hayes C; Rump A; Cadman MR; Harrison M; Evans EP; Lyon MF; Morriss-Kay GM; Rosenthal A; Brown SD
Genomics; 2001 Dec; 78(3):197-205. PubMed ID: 11735226
[TBL] [Abstract][Full Text] [Related]
13. A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.
Heus HC; Hing A; van Baren MJ; Joosse M; Breedveld GJ; Wang JC; Burgess A; Donnis-Keller H; Berglund C; Zguricas J; Scherer SW; Rommens JM; Oostra BA; Heutink P
Genomics; 1999 May; 57(3):342-51. PubMed ID: 10329000
[TBL] [Abstract][Full Text] [Related]
14. A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.
Masuya H; Sezutsu H; Sakuraba Y; Sagai T; Hosoya M; Kaneda H; Miura I; Kobayashi K; Sumiyama K; Shimizu A; Nagano J; Yokoyama H; Kaneko S; Sakurai N; Okagaki Y; Noda T; Wakana S; Gondo Y; Shiroishi T
Genomics; 2007 Feb; 89(2):207-14. PubMed ID: 17049204
[TBL] [Abstract][Full Text] [Related]
15. High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6.
Weber JS; Jang W; Simin K; Lu W; Yu J; Meisler MH
Genomics; 1998 Nov; 54(1):107-15. PubMed ID: 9806835
[TBL] [Abstract][Full Text] [Related]
16. The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.
Gorman SW; Haider NB; Grieshammer U; Swiderski RE; Kim E; Welch JW; Searby C; Leng S; Carmi R; Sheffield VC; Duhl DM
Genomics; 1999 Jul; 59(2):150-60. PubMed ID: 10409426
[TBL] [Abstract][Full Text] [Related]
17. Analysis of limb patterning in BMP-7-deficient mice.
Hofmann C; Luo G; Balling R; Karsenty G
Dev Genet; 1996; 19(1):43-50. PubMed ID: 8792608
[TBL] [Abstract][Full Text] [Related]
18. HnRNP U mediates the long-range regulation of Shh expression during limb development.
Zhao J; Ding J; Li Y; Ren K; Sha J; Zhu M; Gao X
Hum Mol Genet; 2009 Aug; 18(16):3090-7. PubMed ID: 19477957
[TBL] [Abstract][Full Text] [Related]
19. Deletion of a conserved noncoding sequence in Plzf intron leads to Plzf down-regulation in limb bud and polydactyly in the rat.
Liska F; Snajdr P; Sedová L; Seda O; Chylíková B; Slámová P; Krejcí E; Sedmera D; Grim M; Krenová D; Kren V
Dev Dyn; 2009 Mar; 238(3):673-84. PubMed ID: 19191224
[TBL] [Abstract][Full Text] [Related]
20. Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp).
Eddleston J; Murdoch JN; Copp AJ; Stanier P
Genomics; 1999 Mar; 56(2):149-59. PubMed ID: 10051400
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]