Hennies HC - Search Results

1

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).

Reis A, Hennies HC, Langbein L, Digweed M, Mischke D, Drechsler M, Schröck E, Royer-Pokora B, Franke WW, Sperling K, et al. Reis A, et al. Among authors: hennies hc. Nat Genet. 1994 Feb;6(2):174-9. doi: 10.1038/ng0294-174. Nat Genet. 1994. PMID: 7512862

2

Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.

Wolf MT, Zalewski I, Martin FC, Ruf R, Müller D, Hennies HC, Schwarz S, Panther F, Attanasio M, Acosta HG, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Nieto VG, Hildebrandt F. Wolf MT, et al. Among authors: hennies hc. Nephrol Dial Transplant. 2005 May;20(5):909-14. doi: 10.1093/ndt/gfh754. Epub 2005 Mar 1. Nephrol Dial Transplant. 2005. PMID: 15741201

3

Telomeric refinement of the MCKD1 locus on chromosome 1q21.

Wolf MT, van Vlem B, Hennies HC, Zalewski I, Karle SM, Puetz M, Panther F, Otto E, Fuchshuber A, Lameire N, Loeys B, Hildebrandt F. Wolf MT, et al. Among authors: hennies hc. Kidney Int. 2004 Aug;66(2):580-5. doi: 10.1111/j.1523-1755.2004.00799.x. Kidney Int. 2004. PMID: 15253709 Free article.

4

A novel homozygous missense mutation in SLURP1 causing Mal de Meleda with an atypical phenotype.

Gruber R, Hennies HC, Romani N, Schmuth M. Gruber R, et al. Among authors: hennies hc. Arch Dermatol. 2011 Jun;147(6):748-50. doi: 10.1001/archdermatol.2011.138. Arch Dermatol. 2011. PMID: 21690549 No abstract available.

5

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

Ruf RG, Wolf MT, Hennies HC, Lucke B, Zinn C, Varnholt V, Lichtenberger A, Pasch A, Imm A, Briese S, Lennert T, Fuchshuber A, Nurnberg P, Hildebrandt F. Ruf RG, et al. Among authors: hennies hc. J Am Soc Nephrol. 2003 Jun;14(6):1519-22. doi: 10.1097/01.asn.0000066141.55735.8d. J Am Soc Nephrol. 2003. PMID: 12761252

6

Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.

Spielvogel H, Hennies HC, Claussen U, Washington SS, Chakravarti A, Reis A. Spielvogel H, et al. Among authors: hennies hc. Am J Hum Genet. 1992 May;50(5):1031-7. Am J Hum Genet. 1992. PMID: 1570832 Free PMC article.

7

[Vörner keratosis palmoplantaris diffusa. Clinical, formal genetic and molecular biology studies of 22 families].

Küster W, Zehender D, Mensing H, Hennies HC, Reis A. Küster W, et al. Among authors: hennies hc. Hautarzt. 1995 Oct;46(10):705-10. doi: 10.1007/s001050050326. Hautarzt. 1995. PMID: 7499131 German.

8

Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma.

Hennies HC, Zehender D, Kunze J, Küster W, Reis A. Hennies HC, et al. Hum Genet. 1994 Jun;93(6):649-54. doi: 10.1007/BF00201564. Hum Genet. 1994. PMID: 7516304

9

Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.

Hennies HC, Küster W, Mischke D, Reis A. Hennies HC, et al. Hum Mol Genet. 1995 Jun;4(6):1015-20. doi: 10.1093/hmg/4.6.1015. Hum Mol Genet. 1995. PMID: 7544663

10

Dinucleotide repeat polymorphism at the locus D13S231.

Saksová L, Hennies HC, Reis A. Saksová L, et al. Among authors: hennies hc. Hum Mol Genet. 1993 Jul;2(7):1082. doi: 10.1093/hmg/2.7.1082-a. Hum Mol Genet. 1993. PMID: 8364558 No abstract available.

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