Search Results - "Wöste, M."

Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest by van der Bijl, N, Röpke, A, Biswas, U, Wöste, M, Jessberger, R, Kliesch, S, Friedrich, C, Tüttelmann, F

“…Abstract STUDY QUESTION Are sequence variants in the stromal antigen 3 (STAG3) gene a cause for non-obstructive azoospermia (NOA) in infertile human males?…”
Get full text

Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes by Wyrwoll, M J, van Walree, E S, Hamer, G, Rotte, N, Motazacker, M M, Meijers-Heijboer, H, Alders, M, Meißner, A, Kaminsky, E, Wöste, M, Krallmann, C, Kliesch, S, Hunt, T J, Clark, A T, Silber, S, Stallmeyer, B, Friedrich, C, van Pelt, A M M, Mathijssen, I B, Tüttelmann, F

“…Abstract STUDY QUESTION Do bi-allelic variants in the genes encoding the MSH4/MSH5 heterodimer cause male infertility? SUMMARY ANSWER We detected biallelic,…”
Get full text

Analysis of copy number variation in men with non‐obstructive azoospermia by Wyrwoll, M. J., Wabschke, R., Röpke, A., Wöste, M., Ruckert, C., Perrey, S., Rotte, N., Hardy, J., Astica, L., Lupiáñez, D. G., Wistuba, J., Westernströer, B., Schlatt, S., Berman, A. J., Müller, A. M., Kliesch, S., Yatsenko, A. N., Tüttelmann, F., Friedrich, C.

“…Background Recent findings demonstrate that single nucleotide variants can cause non‐obstructive azoospermia (NOA). In contrast, copy number variants (CNVs)…”
Get full text

O-089 A Genome Wide Association Study in men with unexplained infertility identifies nine SNPs at the FSHB locus to be associated with Follicle Stimulating Hormone level by Schubert, M, Pérez Lanuza, L, Wöste, M, Dugas, M, Rassam, Y, Heilmann-Heimbach, S, Tüttelmann, F, Kliesch, S, Gromoll, J

“…Abstract Study question Which single nucleotide polymorphisms (SNPs) are associated with Follicle stimulating hormone (FSH) levels in men with unexplained…”
Get full text

Identifying a genomic region at Chromosome 11p.14.1 that is associated to FSH serum level in men with unexplained male infertility by Schubert, M., Pérez Lanuza, L., Wöste, M., Dugas, M., Rassam, Y., Heilmann-Heimbach, S., Tüttelmann, F., Kliesch, S., Gromoll, J.

Get full text

P–529 Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes by Persio, S D, Leitão, E, Wöste, M, Tekath, T, Cremers, J F, Dugas, M, Xiaolin, L, Meye. z. Hörste, G, Kliesch, S, Laurentino, S, Horsthemke, B, Neuhaus, N

“…Abstract Study question Do DNA methylation changes occur in testicular germ cells (TGCs) from patients with impaired spermatogenesis? Summary answer TGCs from…”
Get full text