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Items: 16

1.

Early Mandibular Distraction to Relieve Robin Severe Airway Obstruction in Two Siblings with Lymphedema-Distichiasis Syndrome.

Papoff P, Castori M, Manganaro L, Midulla F, Moretti C, Cascone P.

J Maxillofac Oral Surg. 2016 Sep;15(3):384-389. Epub 2015 Mar 18.

PMID:
27752211
2.

Foxl1-expressing mesenchymal cells constitute the intestinal stem cell niche.

Aoki R, Shoshkes-Carmel M, Gao N, Shin S, May CL, Golson ML, Zahm AM, Ray M, Wiser CL, Wright CV, Kaestner KH.

Cell Mol Gastroenterol Hepatol. 2016 Feb 1;2(2):175-188.

3.

Identification of HOXD4 Mutations in Spinal Extradural Arachnoid Cyst.

Ogura Y, Miyake N, Kou I, Iida A, Nakajima M, Takeda K, Fujibayashi S, Shiina M, Okada E, Toyama Y, Iwanami A, Ishii K, Ogata K, Asahara H, Matsumoto N, Nakamura M, Matsumoto M, Ikegawa S.

PLoS One. 2015 Nov 6;10(11):e0142126. doi: 10.1371/journal.pone.0142126. eCollection 2015.

4.

Epigenetic regulation of the intestinal epithelium.

Elliott EN, Kaestner KH.

Cell Mol Life Sci. 2015 Nov;72(21):4139-56. doi: 10.1007/s00018-015-1997-9. Epub 2015 Jul 29. Review.

5.

A five generation family with a novel mutation in FOXC2 and lymphedema worsening to hydrops in the youngest generation.

Sargent C, Bauer J, Khalil M, Filmore P, Bernas M, Witte M, Pearson MP, Erickson RP.

Am J Med Genet A. 2014 Nov;164A(11):2802-7. doi: 10.1002/ajmg.a.36736. Epub 2014 Sep 22.

6.

Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.

Butler MG, Dagenais SL, Garcia-Perez JL, Brouillard P, Vikkula M, Strouse P, Innis JW, Glover TW.

Am J Med Genet A. 2012 Apr;158A(4):839-49. doi: 10.1002/ajmg.a.35229. Epub 2012 Mar 9.

7.

Foxl1-Cre-marked adult hepatic progenitors have clonogenic and bilineage differentiation potential.

Shin S, Walton G, Aoki R, Brondell K, Schug J, Fox A, Smirnova O, Dorrell C, Erker L, Chu AS, Wells RG, Grompe M, Greenbaum LE, Kaestner KH.

Genes Dev. 2011 Jun 1;25(11):1185-92. doi: 10.1101/gad.2027811.

8.

Foxl1 is a marker of bipotential hepatic progenitor cells in mice.

Sackett SD, Li Z, Hurtt R, Gao Y, Wells RG, Brondell K, Kaestner KH, Greenbaum LE.

Hepatology. 2009 Mar;49(3):920-9. doi: 10.1002/hep.22705.

9.

FoxF1 and FoxL1 link hedgehog signaling and the control of epithelial proliferation in the developing stomach and intestine.

Madison BB, McKenna LB, Dolson D, Epstein DJ, Kaestner KH.

J Biol Chem. 2009 Feb 27;284(9):5936-44. doi: 10.1074/jbc.M808103200. Epub 2008 Dec 2.

10.

Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells.

Gadue P, Huber TL, Paddison PJ, Keller GM.

Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16806-11. Epub 2006 Oct 31.

11.

Comparative genomics of vertebrate Fox cluster loci.

Wotton KR, Shimeld SM.

BMC Genomics. 2006 Oct 24;7:271.

12.

Foxl1 is a mesenchymal Modifier of Min in carcinogenesis of stomach and colon.

Perreault N, Sackett SD, Katz JP, Furth EE, Kaestner KH.

Genes Dev. 2005 Feb 1;19(3):311-5. Epub 2005 Jan 13.

13.

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.

Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW.

J Med Genet. 2001 Nov;38(11):761-6.

14.

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW.

Am J Hum Genet. 2000 Dec;67(6):1382-8. Epub 2000 Nov 8.

15.
16.

Forkheads, winged helices, and gastrointestinal epithelium.

Sanderson IR.

Gut. 1997 Dec;41(6):853-4. No abstract available.

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