Scherer G - Search Results

1

Human NK cells require caspases for activation-induced proliferation and cytokine release but not for cytotoxicity.

Ussat S, Scherer G, Fazio J, Beetz S, Kabelitz D, Adam-Klages S. Ussat S, et al. Among authors: scherer g. Scand J Immunol. 2010 Nov;72(5):388-95. doi: 10.1111/j.1365-3083.2010.02449.x. Scand J Immunol. 2010. PMID: 21039733 Free article.

2

Sensitization to death receptor cytotoxicity by inhibition of fas-associated death domain protein (FADD)/caspase signaling. Requirement of cell cycle progression.

Lüschen S, Ussat S, Scherer G, Kabelitz D, Adam-Klages S. Lüschen S, et al. Among authors: scherer g. J Biol Chem. 2000 Aug 11;275(32):24670-8. doi: 10.1074/jbc.M003280200. J Biol Chem. 2000. PMID: 10827087 Free article.

3

Impaired neutral sphingomyelinase activation and cutaneous barrier repair in FAN-deficient mice.

Kreder D, Krut O, Adam-Klages S, Wiegmann K, Scherer G, Plitz T, Jensen JM, Proksch E, Steinmann J, Pfeffer K, Krönke M. Kreder D, et al. Among authors: scherer g. EMBO J. 1999 May 4;18(9):2472-9. doi: 10.1093/emboj/18.9.2472. EMBO J. 1999. PMID: 10228161 Free PMC article.

4

Assignment of the human FAN protein gene (NSMAF) to human chromosome region 8q12-->q13 by in situ hybridization.

Zhang Y, Kreder D, Schwandner R, Krut O, Scherer G, Adam-Klages S, Siebert R, Krönke M, Schlegelberger B. Zhang Y, et al. Among authors: scherer g. Cytogenet Cell Genet. 1999;87(1-2):115-6. doi: 10.1159/000015375. Cytogenet Cell Genet. 1999. PMID: 10640829 No abstract available.

5

Caspase 7-induced cleavage of kinectin in apoptotic cells.

Machleidt T, Geller P, Schwandner R, Scherer G, Krönke M. Machleidt T, et al. Among authors: scherer g. FEBS Lett. 1998 Sep 25;436(1):51-4. doi: 10.1016/s0014-5793(98)01095-3. FEBS Lett. 1998. PMID: 9771892 Free article.

6

Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16.

Natt E, Magenis RE, Zimmer J, Mansouri A, Scherer G. Natt E, et al. Among authors: scherer g. Cytogenet Cell Genet. 1989;50(2-3):145-8. doi: 10.1159/000132745. Cytogenet Cell Genet. 1989. PMID: 2789125

7

Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19.

Saridaki A, Ferraz C, Demaille J, Scherer G, Roux AF. Saridaki A, et al. Among authors: scherer g. Cytogenet Cell Genet. 2000;89(1-2):85-8. doi: 10.1159/000015569. Cytogenet Cell Genet. 2000. PMID: 10894943

8

SOX20, a new member of the SOX gene family, is located on chromosome 17p13.

Meyer J, Wirth J, Held M, Schempp W, Scherer G. Meyer J, et al. Among authors: scherer g. Cytogenet Cell Genet. 1996;72(2-3):246-9. doi: 10.1159/000134200. Cytogenet Cell Genet. 1996. PMID: 8978787

9

A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3.

Wagner T, Tommerup N, Wirth J, Leffers H, Zimmer J, Back E, Weissenbach J, Scherer G. Wagner T, et al. Among authors: scherer g. Cytogenet Cell Genet. 1997;76(3-4):172-5. doi: 10.1159/000134538. Cytogenet Cell Genet. 1997. PMID: 9186513

10

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9.

Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, Wolf U, Tommerup N, Schempp W, Scherer G. Wagner T, et al. Among authors: scherer g. Cell. 1994 Dec 16;79(6):1111-20. doi: 10.1016/0092-8674(94)90041-8. Cell. 1994. PMID: 8001137

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