Engel W - Search Results

1

SALL3, a new member of the human spalt-like gene family, maps to 18q23.

Kohlhase J, Hausmann S, Stojmenovic G, Dixkens C, Bink K, Schulz-Schaeffer W, Altmann M, Engel W. Kohlhase J, et al. Among authors: engel w. Genomics. 1999 Dec 1;62(2):216-22. doi: 10.1006/geno.1999.6005. Genomics. 1999. PMID: 10610715

2

Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt.

Kohlhase J, Schuh R, Dowe G, Kühnlein RP, Jäckle H, Schroeder B, Schulz-Schaeffer W, Kretzschmar HA, Köhler A, Müller U, Raab-Vetter M, Burkhardt E, Engel W, Stick R. Kohlhase J, et al. Among authors: engel w. Genomics. 1996 Dec 15;38(3):291-8. doi: 10.1006/geno.1996.0631. Genomics. 1996. PMID: 8975705

3

Genomic cloning, chromosomal mapping, and expression analysis of msal-2.

Kohlhase J, Altmann M, Archangelo L, Dixkens C, Engel W. Kohlhase J, et al. Among authors: engel w. Mamm Genome. 2000 Jan;11(1):64-8. doi: 10.1007/s003350010012. Mamm Genome. 2000. PMID: 10602995

4

Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2.

Kohlhase J, Köhler A, Jäckle H, Engel W, Stick R. Kohlhase J, et al. Among authors: engel w. Cytogenet Cell Genet. 1999;84(1-2):31-4. doi: 10.1159/000015206. Cytogenet Cell Genet. 1999. PMID: 10343095

5

Isolation and characterization of a novel human gene, NIF3L1, and its mouse ortholog, Nif3l1, highly conserved from bacteria to mammals.

Tascou S, Uedelhoven J, Dixkens C, Nayernia K, Engel W, Burfeind P. Tascou S, et al. Among authors: engel w. Cytogenet Cell Genet. 2000;90(3-4):330-6. doi: 10.1159/000056799. Cytogenet Cell Genet. 2000. PMID: 11124544

6

Alternative splicing, chromosome assignment and subcellular localization of the testicular haploid expressed gene (THEG).

Mannan A, Lücke K, Dixkens C, Neesen J, Kämper M, Engel W, Burfeind P. Mannan A, et al. Among authors: engel w. Cytogenet Cell Genet. 2000;91(1-4):171-9. doi: 10.1159/000056840. Cytogenet Cell Genet. 2000. PMID: 11173852

7

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.

Kohlhase J, Wischermann A, Reichenbach H, Froster U, Engel W. Kohlhase J, et al. Among authors: engel w. Nat Genet. 1998 Jan;18(1):81-3. doi: 10.1038/ng0198-81. Nat Genet. 1998. PMID: 9425907

8

The putative peroxisomal gene Pxt1 is exclusively expressed in the testis.

Grzmil P, Burfeind C, Preuss T, Dixkens C, Wolf S, Engel W, Burfeind P. Grzmil P, et al. Among authors: engel w. Cytogenet Genome Res. 2007;119(1-2):74-82. doi: 10.1159/000109622. Epub 2007 Dec 14. Cytogenet Genome Res. 2007. PMID: 18160785

9

The Hook1 gene is non-functional in the abnormal spermatozoon head shape (azh) mutant mouse.

Mendoza-Lujambio I, Burfeind P, Dixkens C, Meinhardt A, Hoyer-Fender S, Engel W, Neesen J. Mendoza-Lujambio I, et al. Among authors: engel w. Hum Mol Genet. 2002 Jul 1;11(14):1647-58. doi: 10.1093/hmg/11.14.1647. Hum Mol Genet. 2002. PMID: 12075009

10

Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

Kohlhase J, Taschner PE, Burfeind P, Pasche B, Newman B, Blanck C, Breuning MH, ten Kate LP, Maaswinkel-Mooy P, Mitulla B, Seidel J, Kirkpatrick SJ, Pauli RM, Wargowski DS, Devriendt K, Proesmans W, Gabrielli O, Coppa GV, Wesby-van Swaay E, Trembath RC, Schinzel AA, Reardon W, Seemanova E, Engel W. Kohlhase J, et al. Among authors: engel w. Am J Hum Genet. 1999 Feb;64(2):435-45. doi: 10.1086/302238. Am J Hum Genet. 1999. PMID: 9973281 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

938 results

Search Page