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Results: 1 to 20 of 329

1.

Common genetic and epigenetic syndromes.

Adams DJ, Clark DA.

Pediatr Clin North Am. 2015 Apr;62(2):411-26. doi: 10.1016/j.pcl.2014.11.005. Epub 2015 Jan 22. Review.

PMID:
25836705
2.

The neural crest: a versatile organ system.

Zhang D, Ighaniyan S, Stathopoulos L, Rollo B, Landman K, Hutson J, Newgreen D.

Birth Defects Res C Embryo Today. 2014 Sep;102(3):275-98. doi: 10.1002/bdrc.21081. Epub 2014 Sep 16. Review.

PMID:
25227568
3.

Evolutionary and developmental origins of the cardiac neural crest: building a divided outflow tract.

Keyte AL, Alonzo-Johnsen M, Hutson MR.

Birth Defects Res C Embryo Today. 2014 Sep;102(3):309-23. doi: 10.1002/bdrc.21076. Epub 2014 Sep 16. Review.

4.

'Black sheep' that don't leave the double-stranded RNA-binding domain fold.

Gleghorn ML, Maquat LE.

Trends Biochem Sci. 2014 Jul;39(7):328-40. doi: 10.1016/j.tibs.2014.05.003. Epub 2014 Jun 19. Review.

5.

Unilateral Möbius syndrome: two cases and a review of the literature.

Jacob FD, Kanigan A, Richer L, El Hakim H.

Int J Pediatr Otorhinolaryngol. 2014 Aug;78(8):1228-31. doi: 10.1016/j.ijporl.2014.05.036. Epub 2014 Jun 6. Review.

PMID:
24951398
6.

Surgical considerations in 22Q11.2 deletion syndrome.

Kirschner RE, Baylis AL.

Clin Plast Surg. 2014 Apr;41(2):271-82. doi: 10.1016/j.cps.2013.12.002. Review.

PMID:
24607194
7.

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, Vorstman J, Duijff SN, Klaassen PW, Swillen A, Gothelf D, Green T, Weizman A, Van Amelsvoort T, Evers L, Boot E, Shashi V, Hooper SR, Bearden CE, Jalbrzikowski M, Armando M, Vicari S, Murphy DG, Ousley O, Campbell LE, Simon TJ, Eliez S; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Am J Psychiatry. 2014 Jun;171(6):627-39. Review.

8.

The diverse clinical features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome).

Maggadottir SM, Sullivan KE.

J Allergy Clin Immunol Pract. 2013 Nov-Dec;1(6):589-94. doi: 10.1016/j.jaip.2013.08.003. Epub 2013 Oct 9. Review.

PMID:
24565705
9.

Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature.

Moschese V, Martire B, Soresina A, Chini L, Graziani S, Monteferrario E, Bacchetta R, Cancrini C, Fiorilli M, Gambineri E, Pession A, Pignata C, Quinti I, Rondelli R, Rossi P, Ugazio AG, Plebani A, Pietrogrande MC.

J Biol Regul Homeost Agents. 2013 Oct-Dec;27(4):935-46. Review.

PMID:
24382174
10.

Progress in microRNA delivery.

Zhang Y, Wang Z, Gemeinhart RA.

J Control Release. 2013 Dec 28;172(3):962-74. doi: 10.1016/j.jconrel.2013.09.015. Epub 2013 Sep 25. Review.

11.

Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.

Gao S, Li X, Amendt BA.

Curr Allergy Asthma Rep. 2013 Dec;13(6):613-21. doi: 10.1007/s11882-013-0384-6. Review.

12.

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

Jonas RK, Montojo CA, Bearden CE.

Biol Psychiatry. 2014 Mar 1;75(5):351-60. doi: 10.1016/j.biopsych.2013.07.019. Epub 2013 Aug 28. Review.

13.

RNA binding proteins in the regulation of heart development.

Blech-Hermoni Y, Ladd AN.

Int J Biochem Cell Biol. 2013 Nov;45(11):2467-78. doi: 10.1016/j.biocel.2013.08.008. Epub 2013 Aug 20. Review. Erratum in: Int J Biochem Cell Biol. 2014 Oct;55:348.

14.

Cellular functions of the microprocessor.

Macias S, Cordiner RA, Cáceres JF.

Biochem Soc Trans. 2013 Aug;41(4):838-43. doi: 10.1042/BST20130011. Review.

PMID:
23863141
15.

Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.

Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen WL, Wang W.

Gene. 2013 Sep 15;527(1):405-9. doi: 10.1016/j.gene.2013.06.009. Epub 2013 Jun 17. Review.

PMID:
23791650
16.

Improving patient tolerability in immunoglobulin treatment: focus on stabilizer effects.

Sun A, Teschner W, Yel L.

Expert Rev Clin Immunol. 2013 Jun;9(6):577-87. doi: 10.1586/eci.13.39. Review.

PMID:
23730887
17.

Radial microcolumnar cortical architecture: maturational arrest or cortical dysplasia?

Sarnat HB, Flores-Sarnat L.

Pediatr Neurol. 2013 Apr;48(4):259-70. doi: 10.1016/j.pediatrneurol.2012.10.001. Review.

PMID:
23498558
18.

Neuroimaging correlates of 22q11.2 deletion syndrome: implications for schizophrenia research.

Boot E, van Amelsvoort TA.

Curr Top Med Chem. 2012;12(21):2303-13. Review.

PMID:
23279171
19.

Regulation of the MIR155 host gene in physiological and pathological processes.

Elton TS, Selemon H, Elton SM, Parinandi NL.

Gene. 2013 Dec 10;532(1):1-12. doi: 10.1016/j.gene.2012.12.009. Epub 2012 Dec 14. Review.

PMID:
23246696
20.

Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease.

Girardot M, Cavaillé J, Feil R.

Epigenetics. 2012 Dec 1;7(12):1341-8. doi: 10.4161/epi.22884. Epub 2012 Nov 15. Review.

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