Vogt PH - Search Results

1

Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies.

Zink AM, Wohlleber E, Engels H, Rødningen OK, Ravn K, Heilmann S, Rehnitz J, Katzorke N, Kraus C, Blichfeldt S, Hoffmann P, Reutter H, Brockschmidt FF, Kreiß-Nachtsheim M, Vogt PH, Prescott TE, Tümer Z, Lee JA. Zink AM, et al. Among authors: vogt ph. Mol Syndromol. 2014 Feb;5(2):65-75. doi: 10.1159/000357962. Epub 2014 Jan 29. Mol Syndromol. 2014. PMID: 24715853 Free PMC article.

2

FMR1 expression in human granulosa cells and variable ovarian response: control by epigenetic mechanisms.

Rehnitz J, Youness B, Nguyen XP, Dietrich JE, Roesner S, Messmer B, Strowitzki T, Vogt PH. Rehnitz J, et al. Among authors: vogt ph. Mol Hum Reprod. 2021 Feb 5;27(2):gaab001. doi: 10.1093/molehr/gaab001. Mol Hum Reprod. 2021. PMID: 33493269

3

FMR1 and AKT/mTOR Signaling in Human Granulosa Cells: Functional Interaction and Impact on Ovarian Response.

Rehnitz J, Capp E, Messmer B, Nguyen XP, Germeyer A, Freis A, Dietrich JE, Hinderhofer K, Strowitzki T, Vogt PH. Rehnitz J, et al. Among authors: vogt ph. J Clin Med. 2021 Aug 30;10(17):3892. doi: 10.3390/jcm10173892. J Clin Med. 2021. PMID: 34501340 Free PMC article.

4

FMR1 and AKT/mTOR signalling pathways: potential functional interactions controlling folliculogenesis in human granulosa cells.

Rehnitz J, Alcoba DD, Brum IS, Hinderhofer K, Youness B, Strowitzki T, Vogt PH. Rehnitz J, et al. Among authors: vogt ph. Reprod Biomed Online. 2017 Nov;35(5):485-493. doi: 10.1016/j.rbmo.2017.07.016. Epub 2017 Aug 4. Reprod Biomed Online. 2017. PMID: 28826600

5

Variable expression of the Fragile X Mental Retardation 1 (FMR1) gene in patients with premature ovarian failure syndrome is not dependent on number of (CGG)n triplets in exon 1.

Schuettler J, Peng Z, Zimmer J, Sinn P, von Hagens C, Strowitzki T, Vogt PH. Schuettler J, et al. Among authors: vogt ph. Hum Reprod. 2011 May;26(5):1241-51. doi: 10.1093/humrep/der018. Epub 2011 Feb 18. Hum Reprod. 2011. PMID: 21335413

6

Human Y chromosome microdeletion analysis by PCR multiplex protocols identifying only clinically relevant AZF microdeletions.

Vogt PH, Bender U. Vogt PH, et al. Methods Mol Biol. 2013;927:187-204. doi: 10.1007/978-1-62703-038-0_17. Methods Mol Biol. 2013. PMID: 22992914

7

Analyses of Gonadoblastoma Y (GBY)-locus and of Y centromere in Turner syndrome patients.

Knauer-Fischer S, Besikoglu B, Inta I, Kneppo C, Vogt PH, Bettendorf M. Knauer-Fischer S, et al. Among authors: vogt ph. Exp Clin Endocrinol Diabetes. 2015 Jan;123(1):61-5. doi: 10.1055/s-0034-1387734. Epub 2014 Oct 14. Exp Clin Endocrinol Diabetes. 2015. PMID: 25314650 Clinical Trial.

8

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11.

Vogt PH, Edelmann A, Kirsch S, Henegariu O, Hirschmann P, Kiesewetter F, Köhn FM, Schill WB, Farah S, Ramos C, Hartmann M, Hartschuh W, Meschede D, Behre HM, Castel A, Nieschlag E, Weidner W, Gröne HJ, Jung A, Engel W, Haidl G. Vogt PH, et al. Hum Mol Genet. 1996 Jul;5(7):933-43. doi: 10.1093/hmg/5.7.933. Hum Mol Genet. 1996. PMID: 8817327

9

The AZFa gene DBY (DDX3Y) is widely transcribed but the protein is limited to the male germ cells by translation control.

Ditton HJ, Zimmer J, Kamp C, Rajpert-De Meyts E, Vogt PH. Ditton HJ, et al. Among authors: vogt ph. Hum Mol Genet. 2004 Oct 1;13(19):2333-41. doi: 10.1093/hmg/ddh240. Epub 2004 Aug 4. Hum Mol Genet. 2004. PMID: 15294876

10

Human Y chromosome deletions in Yq11 and male fertility.

Vogt PH. Vogt PH. Adv Exp Med Biol. 1997;424:17-30. doi: 10.1007/978-1-4615-5913-9_2. Adv Exp Med Biol. 1997. PMID: 9361758 Review.

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