Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Peter H Vogt"'
Publikováno v:
Reproduction and Fertility, Vol 2, Iss 2, Pp 151-160 (2021)
The Ubiquitous Transcribed Y (UTY a.k.a. KDM6C) AZFa candidate gene on the human Y chromosome and its paralog on the X chromosome, UTX (a.k.a. KDM6A), encode a histone lysine demethylase removing chromatin H3K27 methylation marks at genes transcripti
Externí odkaz:
https://doaj.org/article/e7d7d4441e9b4365b38cc179ffb0ab9c
Publikováno v:
Scientific Reports. 12
Translational control is a major level of gene expression regulation in the male germ line. DDX3Y located in the AZFa region of the human Y chromosome encodes a conserved RNA helicase important for translational control at the G1-S phase of the cell
Autor:
Xuan Phuoc Nguyen, Edison Capp, Jens-Erik Dietrich, Ariane Germeyer, Alexander Freis, Peter H. Vogt, Thomas Strowitzki, Karin Hinderhofer, J. Rehnitz, Birgitta Messmer
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 17
Journal of Clinical Medicine, Vol 10, Iss 3892, p 3892 (2021)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Volume 10
Issue 17
Journal of Clinical Medicine, Vol 10, Iss 3892, p 3892 (2021)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
We aimed to determine whether a functional link with impact on female ovarian reserve exists between FMR1 expression and expression ratios of AKT/mTOR signaling genes in human granulosa cells in vivo, as suggested from prior in vitro data. Three hund
Publikováno v:
Cell & Bioscience, Vol 11, Iss 1, Pp 1-13 (2021)
Cell & Bioscience
Cell & Bioscience
Genomic AZFb deletions in Yq11 coined “classical” (i.e. length of Y DNA deletion: 6.23 Mb) are associated with meiotic arrest (MA) of patient spermatogenesis, i.e., absence of any postmeiotic germ cells. These AZFb deletions are caused by non-all
Autor:
Xuan Phuoc Nguyen, Sabine Roesner, Peter H. Vogt, Berthe Youness, JE Dietrich, J. Rehnitz, Thomas Strowitzki, Birgitta Messmer
Publikováno v:
Molecular Human Reproduction. 27
In humans, FMR1 (fragile X mental retardation 1) is strongly expressed in granulosa cells (GCs) of the female germline and apparently controls efficiency of folliculogenesis. Major control mechanism(s) of the gene transcription rate seem to be based
Autor:
T. Strowitzki, Edison Capp, Birgitta Messmer, Ariane Germeyer, Peter H. Vogt, J. Rehnitz, JE Dietrich
Publikováno v:
Geburtshilfe und Frauenheilkunde.
Publikováno v:
Gynäkologische Endokrinologie. 16:230-239
Genetische Ursachen bei pramaturer Ovarialinsuffizienz („premature ovarian insufficiency“ [POI]) sind in ihrer Inzidenz und klinischen Relevanz sehr unterschiedlich. Teilweise handelt es sich bei den in der Literatur dokumentierten genetischen Ur
Autor:
Peter H. Vogt, Markus Bettendorf, J. Zimmer, B Besikoglu, U. Bender, Peter Sinn, S Knauer-Fischer, T. Strowitzki, Petra Frank-Herrmann, P H Heidemann, Daniela Choukair, Y-F C Lau
Study question Which Y genes mapped to the 'Gonadoblastoma Y (GBY)' locus on human Y chromosome are expressed in germ cells of individuals with some Differences of Sexual Development (DSD) and a Y chromosome in their karyotype (DSD-XY groups)? Summar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7be9d1dfbf58c663cba5af21a3d4de10
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/80287
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/80287
Publikováno v:
Der Gynäkologe. 49:94-100
Bei angeborenen genitalen Fehlbildungen ist haufig entweder die Gonade fehl angelegt (Storung der sexuellen Determinierung) oder es liegt eine endokrinologische Ursache vor, die in Form einer Storung der Androgenproduktion oder -wirkung zu einer gest