Engel H - Search Results

1

Genes for human general transcription initiation factors TFIIIB, TFIIIB-associated proteins, TFIIIC2 and PTF/SNAPC: functional and positional candidates for tumour predisposition or inherited genetic diseases?

Purrello M, Di Pietro C, Rapisarda A, Amico V, Giunta V, Engel H, Stevens S, Hsieh Y, Teichman M, Wang Z, Sichel G, Roeder R, Grzeschik KH. Purrello M, et al. Among authors: engel h. Oncogene. 2001 Aug 9;20(35):4877-83. doi: 10.1038/sj.onc.1204604. Oncogene. 2001. PMID: 11521199

2

Genomics of the human genes encoding four TAFII subunits of TFIID, the three subunits of TFIIA, as well as CDK8 and SURB7.

Di Pietro C, Rapisarda A, Bonaiuto C, Lizzio MN, Engel H, Amico V, Scalia M, Amato A, Grzeschik KH, Sichel G, Purrello M. Di Pietro C, et al. Among authors: engel h. Somat Cell Mol Genet. 1999 May;25(3):185-9. doi: 10.1023/a:1018897624615. Somat Cell Mol Genet. 1999. PMID: 11441538

3

Genomic localization of the human genes TAF1A, TAF1B and TAF1C, encoding TAF(I)48, TAF(I)63 and TAF(I)110 subunits of class I general transcription initiation factor SL1.

Di Pietro C, Rapisarda A, Amico V, Bonaiuto C, Viola A, Scalia M, Motta S, Amato A, Engel H, Messina A, Sichel G, Grzeschik K, Purrello M. Di Pietro C, et al. Among authors: engel h. Cytogenet Cell Genet. 2000;89(1-2):133-6. doi: 10.1159/000015592. Cytogenet Cell Genet. 2000. PMID: 10894955

4

Partial gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel (Kir7.1) gene (KCNJ13).

Derst C, Döring F, Preisig-Müller R, Daut J, Karschin A, Jeck N, Weber S, Engel H, Grzeschik KH. Derst C, et al. Among authors: engel h. Genomics. 1998 Dec 15;54(3):560-3. doi: 10.1006/geno.1998.5598. Genomics. 1998. PMID: 9878260

5

The neurobeachin gene (Nbea) identifies a new region of homology between mouse central chromosome 3 and human chromosome 13q13.

Gilbert DJ, Engel H, Wang X, Grzeschik KH, Copeland NG, Jenkins NA, Kilimann MW. Gilbert DJ, et al. Among authors: engel h. Mamm Genome. 1999 Oct;10(10):1030-1. doi: 10.1007/s003359901154. Mamm Genome. 1999. PMID: 10501977 No abstract available.

6

Genomic structure and chromosome mapping of human and mouse RAMP genes.

Derst C, Engel H, Grzeschik K, Daut J. Derst C, et al. Among authors: engel h. Cytogenet Cell Genet. 2000;90(1-2):115-8. doi: 10.1159/000015644. Cytogenet Cell Genet. 2000. PMID: 11060459

7

Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome.

König A, Happle R, Bornholdt D, Engel H, Grzeschik KH. König A, et al. Among authors: engel h. Am J Med Genet. 2000 Feb 14;90(4):339-46. Am J Med Genet. 2000. PMID: 10710235 Review.

8

Primary gene structure and expression studies of rodent paracellin-1.

Weber S, Schlingmann KP, Peters M, Nejsum LN, Nielsen S, Engel H, Grzeschik KH, Seyberth HW, Gröne HJ, Nüsing R, Konrad M. Weber S, et al. Among authors: engel h. J Am Soc Nephrol. 2001 Dec;12(12):2664-2672. doi: 10.1681/ASN.V12122664. J Am Soc Nephrol. 2001. PMID: 11729235

9

A novel missense mutation of NSDHL in an unusual case of CHILD syndrome showing bilateral, almost symmetric involvement.

König A, Happle R, Fink-Puches R, Soyer HP, Bornholdt D, Engel H, Grzeschik KH. König A, et al. Among authors: engel h. J Am Acad Dermatol. 2002 Apr;46(4):594-6. doi: 10.1067/mjd.2002.113680. J Am Acad Dermatol. 2002. PMID: 11907515

10

Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3.

Lisch W, Büttner A, Oeffner F, Böddeker I, Engel H, Lisch C, Ziegler A, Grzeschik K. Lisch W, et al. Among authors: engel h. Am J Ophthalmol. 2000 Oct;130(4):461-8. doi: 10.1016/s0002-9394(00)00494-3. Am J Ophthalmol. 2000. PMID: 11024418

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