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Items: 12


Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth.

Loveday C, Tatton-Brown K, Clarke M, Westwood I, Renwick A, Ramsay E, Nemeth A, Campbell J, Joss S, Gardner M, Zachariou A, Elliott A, Ruark E, van Montfort R; Childhood Overgrowth Collaboration., Rahman N.

Hum Mol Genet. 2015 Sep 1;24(17):4775-9. doi: 10.1093/hmg/ddv182. Epub 2015 May 13.


Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.

Tatton-Brown K, Murray A, Hanks S, Douglas J, Armstrong R, Banka S, Bird LM, Clericuzio CL, Cormier-Daire V, Cushing T, Flinter F, Jacquemont ML, Joss S, Kinning E, Lynch SA, Magee A, McConnell V, Medeira A, Ozono K, Patton M, Rankin J, Shears D, Simon M, Splitt M, Strenger V, Stuurman K, Taylor C, Titheradge H, Van Maldergem L, Temple IK, Cole T, Seal S; Childhood Overgrowth Consortium., Rahman N.

Am J Med Genet A. 2013 Dec;161A(12):2972-80. doi: 10.1002/ajmg.a.36229. Epub 2013 Nov 8.


Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

Tatton-Brown K, Hanks S, Ruark E, Zachariou A, Duarte Sdel V, Ramsay E, Snape K, Murray A, Perdeaux ER, Seal S, Loveday C, Banka S, Clericuzio C, Flinter F, Magee A, McConnell V, Patton M, Raith W, Rankin J, Splitt M, Strenger V, Taylor C, Wheeler P, Temple KI, Cole T; Childhood Overgrowth Collaboration., Douglas J, Rahman N.

Oncotarget. 2011 Dec;2(12):1127-33.


Effect of cumulus cell coculture and oxygen tension on the in vitro developmental competence of bovine zygotes cultured singly.

Goovaerts IG, Leroy JL, Van Soom A, De Clercq JB, Andries S, Bols PE.

Theriogenology. 2009 Mar 15;71(5):729-38. doi: 10.1016/j.theriogenology.2008.09.038. Epub 2008 Oct 28.


Follicle survival and growth to antral stages in short-term murine ovarian cortical transplants after Cryologic solid surface vitrification or slow-rate freezing.

Aerts JM, De Clercq JB, Andries S, Leroy JL, Van Aelst S, Bols PE.

Cryobiology. 2008 Oct;57(2):163-9. doi: 10.1016/j.cryobiol.2008.07.011. Epub 2008 Aug 7.


Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep.

Coutelier M, Andries S, Ghariani S, Dan B, Duyckaerts C, van Rijckevorsel K, Raftopoulos C, Deconinck N, Sonderegger P, Scaravilli F, Vikkula M, Godfraind C.

Neurology. 2008 Jul 1;71(1):64-6. doi: 10.1212/01.wnl.0000316306.08751.28. No abstract available.


Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly.

Andries S, Sartenaer D, Rack K, Rombout S, Tuerlinckx D, Gillerot Y, Van Maldergem L.

J Med Genet. 2002 Oct;39(10):E60. No abstract available.


Posttransplant immune hepatitis in pediatric liver transplant recipients: incidence and maintenance therapy with azathioprine.

Andries S, Casamayou L, Sempoux C, Burlet M, Reding R, Bernard Otte J, Buts JP, Sokal E.

Transplantation. 2001 Jul 27;72(2):267-72.


Acute poisoning with amphetamines (MDEA) and heroin: antagonistic effects between the two drugs.

Jorens PG, Heytens L, Demey HE, Andries S, Ricaurte GA, Bossaert L, Schepens PJ.

Intensive Care Med. 1996 May;22(5):456-9.


Positive confirmation of identity of doping agents using gas chromatography-mass spectrometry with Fourier transform infrared spectrometry.

Selala MI, Janssens JJ, Coucke V, Andries S, Schepens PJ.

J Chromatogr. 1989 Apr 7;489(1):51-6.


Quantitative determination of nitroglycerin by capillary gas chromatography-electron capture detection.

Janssens JJ, Selala MI, Daelemans FF, Andries SW, Schepens PJ.

J Pharm Biomed Anal. 1989;7(12):1631-4.


[Evaluation of the fluorescence for the identification of Corynebacterium diphtheriae in patients with diphtheria].

Duarte Formiga LC, Andries S, Suassuna I.

Rev Latinoam Microbiol. 1981 Jul-Sep;23(3):131-3. Spanish. No abstract available.


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