Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 17

1.

An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression.

Leushacke M, Spörle R, Bernemann C, Brouwer-Lehmitz A, Fritzmann J, Theis M, Buchholz F, Herrmann BG, Morkel M.

PLoS One. 2011;6(8):e23381. doi: 10.1371/journal.pone.0023381. Epub 2011 Aug 11.

2.

A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C.

Jensen LR, Bartenschlager H, Rujirabanjerd S, Tzschach A, Nümann A, Janecke AR, Spörle R, Stricker S, Raynaud M, Nelson J, Hackett A, Fryns JP, Chelly J, de Brouwer AP, Hamel B, Gecz J, Ropers HH, Kuss AW.

Pathogenetics. 2010 Feb 2;3(1):2. doi: 10.1186/1755-8417-3-2.

3.

Cloning of mouse ojoplano, a reticular cytoplasmic protein expressed during embryonic development.

Mertes F, Martinez-Morales JR, Nolden T, Spörle R, Wittbrodt J, Lehrach H, Himmelbauer H.

Gene Expr Patterns. 2009 Dec;9(8):562-7. doi: 10.1016/j.gep.2009.09.003. Epub 2009 Sep 18.

PMID:
19766735
4.

Multiple roles for neurofibromin in skeletal development and growth.

Kolanczyk M, Kossler N, Kühnisch J, Lavitas L, Stricker S, Wilkening U, Manjubala I, Fratzl P, Spörle R, Herrmann BG, Parada LF, Kornak U, Mundlos S.

Hum Mol Genet. 2007 Apr 15;16(8):874-86. Epub 2007 Feb 22.

PMID:
17317783
5.

Expression of Ndufb11 encoding the neuronal protein 15.6 during neurite outgrowth and development.

Gurok U, Bork K, Nuber U, Spörle R, Nöhring S, Horstkorte R.

Gene Expr Patterns. 2007 Jan;7(3):370-4. Epub 2006 Jul 21.

PMID:
16962385
7.

Computer-based three-dimensional visualization of developmental gene expression.

Streicher J, Donat MA, Strauss B, Spörle R, Schughart K, Müller GB.

Nat Genet. 2000 Jun;25(2):147-52.

PMID:
10835627
8.

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome.

Wang YK, Spörle R, Paperna T, Schughart K, Francke U.

Genomics. 1999 Apr 15;57(2):235-48.

PMID:
10198163
9.

Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a candidate gene for the Miller-Dieker syndrome.

Grimm C, Spörle R, Schmid TE, Adler ID, Adamski J, Schughart K, Graw J.

Hum Mol Genet. 1999 Apr;8(4):697-710.

PMID:
10072440
11.

Somite development: constructing the vertebrate body.

Tajbakhsh S, Spörle R.

Cell. 1998 Jan 9;92(1):9-16. Review. No abstract available.

12.
13.

Neural tube morphogenesis.

Spörle R, Schughart K.

Curr Opin Genet Dev. 1997 Aug;7(4):507-12. Review.

PMID:
9309182
14.

The open brain (opb) mutation maps to mouse chromosome 1.

Günther T, Spörle R, Schughart K.

Mamm Genome. 1997 Aug;8(8):583-5. No abstract available.

PMID:
9250866
15.

The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation.

Nagai T, Aruga J, Takada S, Günther T, Spörle R, Schughart K, Mikoshiba K.

Dev Biol. 1997 Feb 15;182(2):299-313.

16.

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney.

Favor J, Sandulache R, Neuhäuser-Klaus A, Pretsch W, Chatterjee B, Senft E, Wurst W, Blanquet V, Grimes P, Spörle R, Schughart K.

Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13870-5.

17.

Severe defects in the formation of epaxial musculature in open brain (opb) mutant mouse embryos.

Spörle R, Günther T, Struwe M, Schughart K.

Development. 1996 Jan;122(1):79-86.

Supplemental Content

Loading ...
Support Center