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Items: 1 to 50 of 79

1.

A hypomorphic Cbx3 allele causes prenatal growth restriction and perinatal energy homeostasis defects.

Aydin E, Kloos DP, Gay E, Jonker W, Hu L, Bullwinkel J, Brown JP, Manukyan M, Giera M, Singh PB, Fundele R.

J Biosci. 2015 Jun;40(2):325-38.

2.

Expression analysis of proline rich 15 (Prr15) in mouse and human gastrointestinal tumors.

Meunier D, Patra K, Smits R, Hägebarth A, Lüttges A, Jaussi R, Wieduwilt MJ, Quintanilla-Fend L, Himmelbauer H, Fodde R, Fundele RH.

Mol Carcinog. 2011 Jan;50(1):8-15. doi: 10.1002/mc.20692.

PMID:
21061267
3.

Enrichment of brain-related genes on the mammalian X chromosome is ancient and predates the divergence of synapsid and sauropsid lineages.

Kemkemer C, Kohn M, Kehrer-Sawatzki H, Fundele RH, Hameister H.

Chromosome Res. 2009;17(6):811-20. doi: 10.1007/s10577-009-9072-8.

PMID:
19731051
4.

Characterization of a novel obesity phenotype caused by interspecific hybridization.

Singh U, Rizvi F, Yu Y, Shi W, Orth A, Karimi M, Ekström TJ, Plagge A, Kelsey G, Fundele R.

Arch Physiol Biochem. 2008 Dec;114(5):301-30. doi: 10.1080/13813450802542495 .

PMID:
19085233
5.

HP1-beta is required for development of the cerebral neocortex and neuromuscular junctions.

Aucott R, Bullwinkel J, Yu Y, Shi W, Billur M, Brown JP, Menzel U, Kioussis D, Wang G, Reisert I, Weimer J, Pandita RK, Sharma GG, Pandita TK, Fundele R, Singh PB.

J Cell Biol. 2008 Nov 17;183(4):597-606. doi: 10.1083/jcb.200804041.

6.

Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assembly.

Brunner S, Colman D, Travis AJ, Luhmann UF, Shi W, Feil S, Imsand C, Nelson J, Grimm C, Rülicke T, Fundele R, Neidhardt J, Berger W.

Biol Reprod. 2008 Oct;79(4):608-17. doi: 10.1095/biolreprod.107.067454. Epub 2008 Jun 25.

PMID:
18579752
7.

Influence of murine maternal diabetes on placental morphology, gene expression, and function.

Yu Y, Singh U, Shi W, Konno T, Soares MJ, Geyer R, Fundele R.

Arch Physiol Biochem. 2008 Apr;114(2):99-110. doi: 10.1080/13813450802033776 .

PMID:
18484278
8.

Expression and function of the LIM homeobox containing genes Lhx3 and Lhx4 in the mouse placenta.

Tian G, Singh U, Yu Y, Ellsworth BS, Hemberger M, Geyer R, Stewart MD, Behringer RR, Fundele R.

Dev Dyn. 2008 May;237(5):1517-25. doi: 10.1002/dvdy.21546.

9.

An activating mutation in the PDGF receptor-beta causes abnormal morphology in the mouse placenta.

Looman C, Sun T, Yu Y, Zieba A, Ahgren A, Feinstein R, Forsberg H, Hellberg C, Heldin CH, Zhang XQ, Forsberg-Nilsson K, Khoo N, Fundele R, Heuchel R.

Int J Dev Biol. 2007;51(5):361-70.

10.

Carboxypeptidase E in the mouse placenta.

Singh U, Yu Y, Kalinina E, Konno T, Sun T, Ohta H, Wakayama T, Soares MJ, Hemberger M, Fundele RH.

Differentiation. 2006 Dec;74(9-10):648-60.

PMID:
17177860
11.

Intrauterine death, fetal malformation, and delayed pregnancy in Ljungan virus-infected mice.

Samsioe A, Feinstein R, Saade G, Sjöholm A, Hörnfeldt B, Fundele R, Klitz W, Niklasson B.

Birth Defects Res B Dev Reprod Toxicol. 2006 Aug;77(4):251-6.

PMID:
16894624
12.

Expression and function of the gene encoding the voltage-dependent calcium channel beta3-subunit in the mouse placenta.

Singh U, Sun T, Looman C, Heuchel R, Elliott R, Freichel M, Meissner M, Flockerzi V, Fundele R.

Placenta. 2007 May-Jun;28(5-6):412-20. Epub 2006 Jul 5.

PMID:
16822546
13.

Expression and functional analysis of fibulin-1 (Fbln1) during normal and abnormal placental development of the mouse.

Singh U, Sun T, Larsson T, Elliott RW, Kostka G, Fundele RH.

Placenta. 2006 Sep-Oct;27(9-10):1014-21. Epub 2005 Dec 9.

PMID:
16338003
14.

Expression and functional analysis of genes deregulated in mouse placental overgrowth models: Car2 and Ncam1.

Singh U, Sun T, Shi W, Schulz R, Nuber UA, Varanou A, Hemberger MC, Elliott RW, Ohta H, Wakayama T, Fundele R.

Dev Dyn. 2005 Dec;234(4):1034-45.

15.

Widespread disruption of genomic imprinting in adult interspecies mouse (Mus) hybrids.

Shi W, Krella A, Orth A, Yu Y, Fundele R.

Genesis. 2005 Nov;43(3):100-8.

PMID:
16145677
16.

Fetal loss in homozygous mutant Norrie disease mice: a new role of Norrin in reproduction.

Luhmann UF, Meunier D, Shi W, Lüttges A, Pfarrer C, Fundele R, Berger W.

Genesis. 2005 Aug;42(4):253-62.

PMID:
16035034
17.

Choroideremia gene product affects trophoblast development and vascularization in mouse extra-embryonic tissues.

Shi W, van den Hurk JA, Alamo-Bethencourt V, Mayer W, Winkens HJ, Ropers HH, Cremers FP, Fundele R.

Dev Biol. 2004 Aug 1;272(1):53-65.

18.

Heterochromatin and tri-methylated lysine 20 of histone H4 in animals.

Kourmouli N, Jeppesen P, Mahadevhaiah S, Burgoyne P, Wu R, Gilbert DM, Bongiorni S, Prantera G, Fanti L, Pimpinelli S, Shi W, Fundele R, Singh PB.

J Cell Sci. 2004 May 15;117(Pt 12):2491-501. Epub 2004 May 5.

19.

Loss-of-imprinting of Peg1 in mouse interspecies hybrids is correlated with altered growth.

Shi W, Lefebvre L, Yu Y, Otto S, Krella A, Orth A, Fundele R.

Genesis. 2004 May;39(1):65-72.

PMID:
15124229
20.

Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation.

Singh U, Fohn LE, Wakayama T, Ohgane J, Steinhoff C, Lipkowitz B, Schulz R, Orth A, Ropers HH, Behringer RR, Tanaka S, Shiota K, Yanagimachi R, Nuber UA, Fundele R.

Dev Dyn. 2004 May;230(1):149-64.

21.

Genes and development--a workshop report.

Cross JC, Coan PM, Fundele R, Hemberger M, Kibschull M, Ferguson-Smith A.

Placenta. 2004 Apr;25 Suppl A:S39-41. No abstract available.

PMID:
15033305
22.

Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus.

Zechner U, Shi W, Hemberger M, Himmelbauer H, Otto S, Orth A, Kalscheuer V, Fischer U, Elango R, Reis A, Vogel W, Ropers H, Rüschendorf F, Fundele R.

J Evol Biol. 2004 Mar;17(2):453-60.

23.

DNA methylation in placentas of interspecies mouse hybrids.

Schütt S, Florl AR, Shi W, Hemberger M, Orth A, Otto S, Schulz WA, Fundele RH.

Genetics. 2003 Sep;165(1):223-8.

24.

Preferential expression of the G90 gene in post-mitotic cells during mouse embryonic development.

Meunier D, Peters T, Lüttges A, Curfs J, Fundele R.

Anat Embryol (Berl). 2003 Sep;207(2):109-17. Epub 2003 May 27.

PMID:
12768423
25.

Effects of sex chromosome dosage on placental size in mice.

Ishikawa H, Rattigan A, Fundele R, Burgoyne PS.

Biol Reprod. 2003 Aug;69(2):483-8. Epub 2003 Apr 16.

PMID:
12700203
26.

Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis.

Herr A, Meunier D, Müller I, Rump A, Fundele R, Ropers HH, Nuber UA.

Dev Dyn. 2003 Apr;226(4):579-86.

27.

Proliferation and growth factor expression in abnormally enlarged placentas of mouse interspecific hybrids.

Zechner U, Hemberger M, Constância M, Orth A, Dragatsis I, Lüttges A, Hameister H, Fundele R.

Dev Dyn. 2002 Jun;224(2):125-34.

28.

Placental-specific IGF-II is a major modulator of placental and fetal growth.

Constância M, Hemberger M, Hughes J, Dean W, Ferguson-Smith A, Fundele R, Stewart F, Kelsey G, Fowden A, Sibley C, Reik W.

Nature. 2002 Jun 27;417(6892):945-8.

PMID:
12087403
29.

Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals.

Cowell IG, Aucott R, Mahadevaiah SK, Burgoyne PS, Huskisson N, Bongiorni S, Prantera G, Fanti L, Pimpinelli S, Wu R, Gilbert DM, Shi W, Fundele R, Morrison H, Jeppesen P, Singh PB.

Chromosoma. 2002 Mar;111(1):22-36.

PMID:
12068920
30.

Role of Runx genes in chondrocyte differentiation.

Stricker S, Fundele R, Vortkamp A, Mundlos S.

Dev Biol. 2002 May 1;245(1):95-108.

31.

Genome-wide methylation patterns in normal and uniparental early mouse embryos.

Barton SC, Arney KL, Shi W, Niveleau A, Fundele R, Surani MA, Haaf T.

Hum Mol Genet. 2001 Dec 15;10(26):2983-7.

PMID:
11751680
32.

A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution?

Zechner U, Wilda M, Kehrer-Sawatzki H, Vogel W, Fundele R, Hameister H.

Trends Genet. 2001 Dec;17(12):697-701.

PMID:
11718922
33.

UniGene cDNA array-based monitoring of transcriptome changes during mouse placental development.

Hemberger M, Cross JC, Ropers HH, Lehrach H, Fundele R, Himmelbauer H.

Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13126-31.

34.

Genetic and developmental analysis of X-inactivation in interspecific hybrid mice suggests a role for the Y chromosome in placental dysplasia.

Hemberger M, Kurz H, Orth A, Otto S, Lüttges A, Elliott R, Nagy A, Tan SS, Tam P, Zechner U, Fundele RH.

Genetics. 2001 Jan;157(1):341-8.

35.

Spatial separation of parental genomes during mouse interspecific (Mus musculus x M. spretus) spermiogenesis.

Mayer W, Fundele R, Haaf T.

Chromosome Res. 2000;8(6):555-8. No abstract available.

PMID:
11032324
36.

cDNA subtraction cloning reveals novel genes whose temporal and spatial expression indicates association with trophoblast invasion.

Hemberger M, Himmelbauer H, Ruschmann J, Zeitz C, Fundele R.

Dev Biol. 2000 Jun 1;222(1):158-69.

37.

Active demethylation of the paternal genome in the mouse zygote.

Oswald J, Engemann S, Lane N, Mayer W, Olek A, Fundele R, Dean W, Reik W, Walter J.

Curr Biol. 2000 Apr 20;10(8):475-8.

38.

Silencing of the Y-chromosomal gene tspy during murine evolution.

Schubert S, Dechend F, Skawran B, Kunze B, Winking H, Weile C, Römer I, Hemberger M, Fundele R, Sharma T, Schmidtke J.

Mamm Genome. 2000 Apr;11(4):288-91.

PMID:
10754104
39.

Spatial separation of parental genomes in preimplantation mouse embryos.

Mayer W, Smith A, Fundele R, Haaf T.

J Cell Biol. 2000 Feb 21;148(4):629-34.

40.

Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis.

Mayer W, Hemberger M, Frank HG, Grümmer R, Winterhager E, Kaufmann P, Fundele R.

Dev Dyn. 2000 Jan;217(1):1-10.

41.

Demethylation of the zygotic paternal genome.

Mayer W, Niveleau A, Walter J, Fundele R, Haaf T.

Nature. 2000 Feb 3;403(6769):501-2. No abstract available.

PMID:
10676950
42.

Genome evolution. Global methylation in eutherian hybrids.

Roemer I, Grützner F, Winking H, Haaf T, Orth A, Skidmore L, Antczak D, Fundele R.

Nature. 1999 Sep 9;401(6749):131-2. No abstract available.

PMID:
10490019
43.

Genetic dissection of X-linked interspecific hybrid placental dysplasia in congenic mouse strains.

Hemberger MC, Pearsall RS, Zechner U, Orth A, Otto S, Rüschendorf F, Fundele R, Elliott R.

Genetics. 1999 Sep;153(1):383-90.

44.

Lack of correlation between placenta and offspring size in mouse interspecific crosses.

Kurz H, Zechner U, Orth A, Fundele R.

Anat Embryol (Berl). 1999 Sep;200(3):335-43.

PMID:
10463348
45.

Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame.

Krause R, Hemberger M, Himmelbauer H, Kalscheuer V, Fundele RH.

Gene. 1999 May 17;232(1):35-42.

PMID:
10333519
46.

Expression of the von Hippel-Lindau-binding protein-1 (Vbp1) in fetal and adult mouse tissues.

Hemberger M, Himmelbauer H, Neumann HP, Plate KH, Schwarzkopf G, Fundele R.

Hum Mol Genet. 1999 Feb;8(2):229-36.

PMID:
9931330
47.

Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2.

Zechner U, Scheel S, Hemberger M, Hopp M, Haaf T, Fundele R, Wanker EE, Lehrach H, Wedemeyer N, Himmelbauer H.

Genomics. 1998 Dec 15;54(3):505-10.

PMID:
9878254
48.

Molecular cloning and characterization of murine Mpgc60, a gene predominantly expressed in the intestinal tract.

Krause R, Hemberger M, Messerschmid M, Mayer W, Kothary R, Dixkens C, Fundele R.

Differentiation. 1998 Sep;63(5):285-94.

PMID:
9810707
49.

H19 and Igf2 are expressed and differentially imprinted in neuroectoderm-derived cells in the mouse brain.

Hemberger M, Redies C, Krause R, Oswald J, Walter J, Fundele RH.

Dev Genes Evol. 1998 Sep;208(7):393-402.

PMID:
9732553
50.

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Schwahn U, Lenzner S, Dong J, Feil S, Hinzmann B, van Duijnhoven G, Kirschner R, Hemberger M, Bergen AA, Rosenberg T, Pinckers AJ, Fundele R, Rosenthal A, Cremers FP, Ropers HH, Berger W.

Nat Genet. 1998 Aug;19(4):327-32.

PMID:
9697692

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