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Results: 1 to 20 of 100

Similar articles for PubMed (Select 11100524)

1.

Mutation analysis of human LEFTY A and LEFTY B genes in children with Ivemark syndrome.

Chen WC, Tsai FJ, Wu JY, Shi YR, Wu HC.

Acta Paediatr Taiwan. 2000 Sep-Oct;41(5):259-62.

PMID:
11100524
2.

Characterization of nodal/TGF-lefty signaling pathway gene variants for possible roles in congenital heart diseases.

Deng X, Zhou J, Li FF, Yan P, Zhao EY, Hao L, Yu KJ, Liu SL.

PLoS One. 2014 Aug 11;9(8):e104535. doi: 10.1371/journal.pone.0104535. eCollection 2014.

3.

Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation.

Brunetti-Pierri N, Del Gaudio D, Peters H, Justino H, Ott CE, Mundlos S, Bacino CA.

Am J Med Genet A. 2008 Nov 1;146A(21):2804-9. doi: 10.1002/ajmg.a.32530.

PMID:
18831060
4.

Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome.

Narumi Y, Aoki Y, Niihori T, Sakurai M, Cavé H, Verloes A, Nishio K, Ohashi H, Kurosawa K, Okamoto N, Kawame H, Mizuno S, Kondoh T, Addor MC, Coeslier-Dieux A, Vincent-Delorme C, Tabayashi K, Aoki M, Kobayashi T, Guliyeva A, Kure S, Matsubara Y.

J Hum Genet. 2008;53(9):834-41. doi: 10.1007/s10038-008-0320-0. Epub 2008 Jul 24.

PMID:
18651097
5.

Lefty acts as an essential modulator of Nodal activity during sea urchin oral-aboral axis formation.

Duboc V, Lapraz F, Besnardeau L, Lepage T.

Dev Biol. 2008 Aug 1;320(1):49-59. doi: 10.1016/j.ydbio.2008.04.012. Epub 2008 Apr 20.

6.

Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits.

Páez MT, Yamamoto T, Hayashi K, Yasuda T, Harada N, Matsumoto N, Kurosawa K, Furutani Y, Asakawa S, Shimizu N, Matsuoka R.

Am J Med Genet A. 2008 May 1;146A(9):1158-65. doi: 10.1002/ajmg.a.32205.

PMID:
18393291
7.

Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies.

Aune CN, Chatterjee B, Zhao XQ, Francis R, Bracero L, Yu Q, Rosenthal J, Leatherbury L, Lo CW.

Pediatr Res. 2008 Jan;63(1):9-14.

PMID:
18043505
8.

Shprintzen-Goldberg syndrome associated with a novel missense mutation in TGFBR2.

van Steensel MA, van Geel M, Parren LJ, Schrander-Stumpel CT, Marcus-Soekarman D.

Exp Dermatol. 2008 Apr;17(4):362-5. Epub 2007 Nov 2.

PMID:
17979970
9.

Lefty longevity: another study.

[No authors listed]

Science. 1994 Mar 18;263(5153):1567. No abstract available.

PMID:
17744782
10.

Xenopus Lefty requires proprotein cleavage but not N-linked glycosylation to inhibit nodal signaling.

Westmoreland JJ, Takahashi S, Wright CV.

Dev Dyn. 2007 Aug;236(8):2050-61.

11.

Novel TBX5 mutations in patients with Holt-Oram syndrome.

Debeer P, Race V, Gewillig M, Devriendt K, Frijns JP.

Clin Orthop Relat Res. 2007 Sep;462:20-6.

PMID:
17534187
12.

Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.

Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, Halimi P, Roche O, Van Regemorter N, Munier F, Schorderet D, Dufier JL, Marsac C, Ricquier D, Menasche M, Penfornis A, Abitbol M.

Mol Vis. 2007 Apr 2;13:511-23.

13.

[Molecular diagnosis of CHARGE syndrom].

Pedersen AM, Skovby F.

Ugeskr Laeger. 2007 Jan 29;169(5):402-6. Review. Danish.

PMID:
17280632
14.

ZFHX1B mutations in patients with Mowat-Wilson syndrome.

Dastot-Le Moal F, Wilson M, Mowat D, Collot N, Niel F, Goossens M.

Hum Mutat. 2007 Apr;28(4):313-21.

PMID:
17203459
15.

Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.

Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M.

Mol Vis. 2006 Dec 1;12:1448-60.

16.

Flounder and fugu have a single lefty gene that covers the functions of lefty1 and lefty2 of zebrafish during L-R patterning.

Hashimoto H, Uji S, Kurokawa T, Washio Y, Suzuki T.

Gene. 2007 Jan 31;387(1-2):126-32. Epub 2006 Sep 14.

PMID:
17084042
17.

Molecular analysis of LEFTY-expressing cells in early human embryoid bodies.

Dvash T, Sharon N, Yanuka O, Benvenisty N.

Stem Cells. 2007 Feb;25(2):465-72. Epub 2006 Oct 12.

18.

DNA mutation analysis in heterotaxy.

Ware SM.

Methods Mol Med. 2006;126:247-56.

PMID:
16930017
19.

Expanding the spectrum of TBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations.

Borozdin W, Bravo Ferrer Acosta AM, Bamshad MJ, Botzenhart EM, Froster UG, Lemke J, Schinzel A, Spranger S, McGaughran J, Wand D, Chrzanowska KH, Kohlhase J.

Hum Mutat. 2006 Sep;27(9):975-6.

PMID:
16917909
20.

Ivemark syndrome in association with congenital septum transversum defect and pancreatic divisum.

Sharma S, Gangopadhyay AN, Sharma SP.

Indian J Gastroenterol. 2006 Mar-Apr;25(2):94-6.

PMID:
16763342
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