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Items: 24


Fine-tuning the onset of myogenesis by homeobox proteins that interact with the Myf5 limb enhancer.

Daubas P, Duval N, Bajard L, Langa Vives F, Robert B, Mankoo BS, Buckingham M.

Biol Open. 2015 Nov 4;4(12):1614-24. doi: 10.1242/bio.014068.


Nop-7-associated 2 (NSA2), a candidate gene for diabetic nephropathy, is involved in the TGFβ1 pathway.

Shahni R, Czajka A, Mankoo BS, Guvenel AK, King AJ, Malik AN.

Int J Biochem Cell Biol. 2013 Mar;45(3):626-35. doi: 10.1016/j.biocel.2012.11.020. Epub 2012 Dec 7.


Transient activation of meox1 is an early component of the gene regulatory network downstream of hoxa2.

Kirilenko P, He G, Mankoo BS, Mallo M, Jones R, Bobola N.

Mol Cell Biol. 2011 Mar;31(6):1301-8. doi: 10.1128/MCB.00705-10. Epub 2011 Jan 18.


Developmental regulation of MURF ubiquitin ligases and autophagy proteins nbr1, p62/SQSTM1 and LC3 during cardiac myofibril assembly and turnover.

Perera S, Holt MR, Mankoo BS, Gautel M.

Dev Biol. 2011 Mar 1;351(1):46-61. doi: 10.1016/j.ydbio.2010.12.024. Epub 2010 Dec 23.


A hypoplastic model of skeletal muscle development displaying reduced foetal myoblast cell numbers, increased oxidative myofibres and improved specific tension capacity.

Otto A, Macharia R, Matsakas A, Valasek P, Mankoo BS, Patel K.

Dev Biol. 2010 Jul 1;343(1-2):51-62. doi: 10.1016/j.ydbio.2010.04.014. Epub 2010 Apr 22.


Retinoic acid is both necessary for and inhibits myogenic commitment and differentiation in the chick limb.

Reijntjes S, Francis-West P, Mankoo BS.

Int J Dev Biol. 2010;54(1):125-34. doi: 10.1387/ijdb.082783sr.


A comparative analysis of Meox1 and Meox2 in the developing somites and limbs of the chick embryo.

Reijntjes S, Stricker S, Mankoo BS.

Int J Dev Biol. 2007;51(8):753-9.


The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites.

Mankoo BS, Skuntz S, Harrigan I, Grigorieva E, Candia A, Wright CV, Arnheiter H, Pachnis V.

Development. 2003 Oct;130(19):4655-64.


Differential activities of the RET tyrosine kinase receptor isoforms during mammalian embryogenesis.

de Graaff E, Srinivas S, Kilkenny C, D'Agati V, Mankoo BS, Costantini F, Pachnis V.

Genes Dev. 2001 Sep 15;15(18):2433-44.


Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors.

Stamataki D, Kastrinaki M, Mankoo BS, Pachnis V, Karagogeos D.

FEBS Lett. 2001 Jun 22;499(3):274-8.


Isolation of the avian homologue of the homeobox gene Mox2 and analysis of its expression pattern in developing somites and limbs.

Rallis C, Stamataki D, Pontikakis S, Mankoo BS, Karagogeos D.

Mech Dev. 2001 Jun;104(1-2):121-4.


Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D.

Am J Hum Genet. 2001 Mar;68(3):661-73.


Mox2 is a component of the genetic hierarchy controlling limb muscle development.

Mankoo BS, Collins NS, Ashby P, Grigorieva E, Pevny LH, Candia A, Wright CV, Rigby PW, Pachnis V.

Nature. 1999 Jul 1;400(6739):69-73.


Linkage study of the D5 dopamine receptor gene (DRD5) in multiplex Icelandic and English schizophrenia pedigrees.

Kalsi G, Sherrington R, Mankoo BS, Brynjolfsson J, Sigmundsson T, Curtis D, Read T, Murphy P, Butler R, Petursson H, Gurling HM.

Am J Psychiatry. 1996 Jan;153(1):107-9.


Exclusion of linkage of schizophrenia to the gene for the dopamine D2 receptor (DRD2) and chromosome 11q translocation sites.

Kalsi G, Mankoo BS, Curtis D, Brynjolfsson J, Read T, Sharma T, Murphy P, Petursson H, Gurling HM.

Psychol Med. 1995 May;25(3):531-7.


The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia.

Kalsi G, Mankoo BS, Brynjolfsson J, Curtis D, Read T, Murphy P, Sharma T, Petursson H, Gurling HM.

Psychiatr Genet. 1994 Winter;4(4):219-27.


A polymorphic microsatellite repeat is located close to the promoter region of the c-fgr proto-oncogene (FGR) at chromosome 1p36.2-p36.1.

Patel MS, Mankoo BS, Brickell PM.

Hum Mol Genet. 1992 Apr;1(1):65. No abstract available.


Stereospecific effect of flupenthixol on neuroreceptor gene expression.

De La Concha A, McKie J, Hodgkinson S, Mankoo BS, Gurling HM.

Brain Res Mol Brain Res. 1991 May;10(2):123-7.


Two microsatellite polymorphisms at the D5S39 locus.

Mankoo BS, Sherrington R, De La Concha A, Kalsi G, Curtis D, Melmer G, Gurling HM.

Nucleic Acids Res. 1991 Apr 25;19(8):1963. No abstract available.


A TaqI polymorphism detected by a genomic clone at the locus D5S39 (5q11-13).

Mankoo BS, Melmer G, Kalsi G, Sherrington R, Gurling HM.

Nucleic Acids Res. 1991 Apr 11;19(7):1720. No abstract available.


Human pro alpha 1(III) collagen: cDNA sequence for the 3' end.

Mankoo BS, Dalgleish R.

Nucleic Acids Res. 1988 Mar 25;16(5):2337. No abstract available.


An anonymous genomic probe (p lambda KP20.1) detects a multi-allelic locus on chromosome 19 (D19S25).

Mankoo BS, Dalgleish R.

Nucleic Acids Res. 1988 Feb 25;16(4):1643. No abstract available.


An anonymous genomic probe (p lambda KP20.1) detects a multi-allelic locus on chromosome 19 (D19S25).

Mankoo BS, Dalgleish R.

Nucleic Acids Res. 1987 Nov 11;15(21):9105. No abstract available.

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