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Literature citations Results

X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.

Yatsenko A.N., Georgiadis A.P., Roepke A., Berman A.J., Jaffe T., Olszewska M., Westernstroeer B., Sanfilippo J., Kurpisz M., Rajkovic A. et al.

N. Engl. J. Med. 372:2097-2107(2015) · UniProtKB (1)

The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men.

Borgmann J., Tuettelmann F., Dworniczak B., Roepke A., Song H.W., Kliesch S., Wilkinson M.F., Laurentino S., Gromoll J.

Hum. Mol. Genet. 25:4898-4910(2016) · UniProtKB (3)

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.

Rauch A., Wieczorek D., Graf E., Wieland T., Endele S., Schwarzmayr T., Albrecht B., Bartholdi D., Beygo J., Di Donato N. et al.

Lancet 380:1674-1682(2012) · UniProtKB (2)

Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer.

Roepke A., Buhtz P., Boehm M., Seger J., Wieland I., Allhoff E.P., Wieacker P.F.

Oncogene 24:6667-6675(2005) · UniProtKB (1)

Oligophrenin-1 (Ophn1) is expressed in mouse retinal vessels.

Sel S., Kaiser M., Nass N., Trau S., Roepke A., Storsberg J., Hampel U., Paulsen F., Kalinski T.

Gene Expr. Patterns 12:63-67(2012) · Mapped (8)

Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cells.

Wieland I., Roepke A., Stumm M., Sell C., Weidle U.H., Wieacker P.F.

Oncol. Res. 12:491-500(2001) · UniProtKB (1) · Mapped (6)

Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome.

Roepke A., Kujat A., Graeber M., Giannakudis J., Hansmann I.

Hum. Mutat. 21:100-100(2003) · UniProtKB (1) · Mapped (6)

A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.

Wieland I., Sabathil J., Ostendorf A., Rittinger O., Roepke A., Winnepenninckx B., Kooy F., Holinski-Feder E., Wieacker P.

Neurogenetics 6:45-47(2005) · UniProtKB (1)

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