Startseite Universitätsklinikum Heidelberg
Startseite Universitätsklinikum Heidelberg Gynäkologische Endokrinologie und Fertilitätsstörungen Teil der Frauenklinik (Zentrum)
Gynäkologische Endokrinologie und Fertilitätsstörungen Teil der Frauenklinik (Zentrum)
Kliniken &… Kliniken Frauenklinik Gynäkologische… Über uns Publikationen

Literaturhinweise

Sektion Reproduktionsgenetik

PubMed gelistet:

  1. Gonadoblastoma Y locus genes expressed in germ cells of individuals with dysgenetic gonads and a Y chromosome in their karyotypes include DDX3Y and TSPY.  Vogt PH, Besikoglu B, Bettendorf M, Frank-Herrmann P, Zimmer J, Bender U, Knauer-Fischer S, Choukair D, Sinn P, Lau YC, Heidemann PH, Strowitzki T. Hum Reprod. 2019 Apr 1;34(4):770-779. doi: 10.1093/humrep/dez004.
  2. FMR1 expression in human granulosa cells increases with exon 1 CGG repeat length depending on ovarian reserve. Rehnitz J, Alcoba DD, Brum IS, Dietrich JE, Youness B, Hinderhofer K, Messmer B, Freis A, Strowitzki T, Germeyer A. Reprod Biol Endocrinol. 2018 Jul 7;16(1):65. doi: 10.1186/s12958-018-0383-5.
  3. 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. Reprod Biomed Online. 2017 Nov;35(5):485-493. doi: 10.1016/j.rbmo.2017.07.016.
  4. Detection of cross-sex chimerism in the common marmoset monkey (Callithrix jacchus) in interphase cells using fluorescence in situ hybridisation probes specific for the marmoset X and Y chromosomes. Wedi E, Müller S, Neusser M, Vogt PH, Tkachenko OY, Zimmer J, Smeets D, Michelmann HW, Nayudu PL. Reprod Fertil Dev. 2016 Feb 15. doi: 10.1071/RD15321.
  5. 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. Exp Clin Endocrinol Diabetes. 2015 Jan;123(1):61-5. doi: 10.1055/s-0034-1387734.
  6. DDX3X, the X homologue of AZFa gene DDX3Y, expresses a complex pattern of transcript variants only in the male germ line. Rauschendorf MA, Zimmer J, Ohnmacht C, Vogt PH.
    Mol Hum Reprod. 2014 Dec;20(12):1208-22. doi: 10.1093/molehr/gau081.
  7. 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. Mol Syndromol. 2014 Feb;5(2):65-75. doi: 10.1159/000357962.
  8. Single nucleotide polymorphism array analysis in men with idiopathic azoospermia or oligoasthenozoospermia syndrome. Frühmesser A, Vogt PH, Zimmer J, Witsch-Baumgartner M, Fauth C, Zschocke J, Pinggera GM, Kotzot D. Fertil Steril. 2013 Jul;100(1):81-7. doi: 10.1016/j.fertnstert.2013.03.016.
  9. Human Y chromosome microdeletion analysis by PCR multiplex protocols identifying only clinically relevant AZF microdeletions. Vogt PH, Bender U. Methods Mol Biol. 2013;927:187-204.
  10. AZFa protein DDX3Y is differentially expressed in human male germ cells during development and in testicular tumours: new evidence for phenotypic plasticity of germ cells. Gueler B, Sonne SB, Zimmer J, Hilscher B, Hilscher W, Græm N, Rajpert-De Meyts E, Vogt PH. Hum Reprod. 2012 Jun;27(6):1547-55. doi: 10.1093/humrep/des047.
  11. 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. Hum Reprod. 2011 May;26(5):1241-51. doi: 10.1093/humrep/der018.
  12. Translational control of the AZFa gene DDX3Y by 5'UTR exon-T extension. Jaroszynski L, Zimmer J, Fietz D, Bergmann M, Kliesch S, Vogt PH. Int J Androl. 2011 Aug;34(4):313-26. doi: 10.1111/j.1365-2605.2010.01079.x.
  13. Complex transcriptional control of the AZFa gene DDX3Y in human testis. Rauschendorf MA, Zimmer J, Hanstein R, Dickemann C, Vogt PH. Int J Androl. 2011 Feb;34(1):84-96. doi: 10.1111/j.1365-2605.2010.01053.x.
  14. A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure. Corre T, Schuettler J, Bione S, Marozzi A, Persani L, Rossetti R, Torricelli F, Giotti I, Vogt P, Toniolo D; Italian Network for the study of Ovarian Dysfunctions. Hum Reprod. 2009 Aug;24(8):2023-8. doi: 10.1093/humrep/dep090. Epub 2009 Apr 10.
  15. The AZF proteins. Vogt PH, Falcao CL, Hanstein R, Zimmer J. Int J Androl. 2008 Aug;31(4):383-94. doi: 10.1111/j.1365-2605.2008.00890.x. Review.
  16. Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea. Gallardo TD, John GB, Bradshaw K, Welt C, Reijo-Pera R, Vogt PH, Touraine P, Bione S, Toniolo D, Nelson LM, Zinn AR, Castrillon DH. Hum Reprod. 2008 Jan;23(1):216-21. Epub 2007 Oct 23.
  17. Premature ovarian failure (POF) syndrome: towards the molecular clinical analysis of its genetic complexity.Fassnacht W, Mempel A, Strowitzki T, Vogt PH. Curr Med Chem. 2006;13(12):1397-410. Review.
  18. Polymorphisms associated with the DAZ genes on the human Y chromosome. Lin YW, Thi DA, Kuo PL, Hsu CC, Huang BD, Yu YH, Vogt PH, Krause W, Ferlin A, Foresta C, Bienvenu T, Schempp W, Yen PH. Genomics. 2005 Oct;86(4):431-8.
  19. AZF deletions and Y chromosomal haplogroups: history and update based on sequence.Vogt PH. Hum Reprod Update. 2005 Jul-Aug;11(4):319-36. Epub 2005 May 12. Review.
  20. Three new 46,XX male patients: a clinical, cytogenetic and molecular analysis. Grigorescu-Sido A, Heinrich U, Grigorescu-Sido P, Jauch A, Hager HD, Vogt PH, Duncea I, Bettendorf M.J Pediatr Endocrinol Metab. 2005 Feb;18(2):197-203.
  21. Azoospermia factor (AZF) in Yq11: towards a molecular understanding of its function for human male fertility and spermatogenesis.Vogt PH. Reprod Biomed Online. 2005 Jan;10(1):81-93.
  22. Introduction: basic science meets the clinic.Vogt PH. Reprod Biomed Online. 2005 Jan;10(1):11-3.
  23. Genomic heterogeneity and instability of the AZF locus on the human Y chromosome. Vogt PH. Mol Cell Endocrinol. 2004 Sep 30;224(1-2):1-9. Review.
  24. 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. Hum Mol Genet. 2004 Oct 1;13(19):2333-41. Epub 2004 Aug 4.
  25. Developmental expression of POU5F1 (OCT-3/4) in normal and dysgenetic human gonads. Rajpert-De Meyts E, Hanstein R, Jørgensen N, Graem N, Vogt PH, Skakkebaek NE. Hum Reprod. 2004 Jun;19(6):1338-44. Epub 2004 Apr 22.
  26. Cytogenetic and molecular analysis of a family with three brothers afflicted with germ-cell cancer. Ottesen AM, Rajpert-De Meyts E, Holm M, Andersen IL, Vogt PH, Lundsteen C, Skakkebaek NE.  Clin Genet. 2004 Jan;65(1):32-9.
  27. Molecular genetics of human male infertility: from genes to new therapeutic perspectives. Vogt PH. Curr Pharm Des. 2004;10(5):471-500. Review.
  28. A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N.
    Fernandes S, Paracchini S, Meyer LH, Floridia G, Tyler-Smith C, Vogt PH. Am J Hum Genet. 2004 Jan;74(1):180-7. Epub 2003 Nov 21.
  29. No AZF deletion in 160 patients with testicular germ cell neoplasia. Frydelund-Larsen L, Vogt PH, Leffers H, Schadwinkel A, Daugaard G, Skakkebaek NE, Rajpert-De Meyts E. Mol Hum Reprod. 2003 Sep;9(9):517-21.
  30. Polymorphic DAZ gene family in polymorphic structure of AZFc locus: Artwork or functional for human spermatogenesis? Vogt PH, Fernandes S. APMIS. 2003 Jan;111(1):115-26; discussion 126-7. Review.
  31. High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia. Fernandes S, Huellen K, Goncalves J, Dukal H, Zeisler J, Rajpert De Meyts E, Skakkebaek NE, Habermann B, Krause W, Sousa M, Barros A, Vogt PH. Mol Hum Reprod. 2002 Mar;8(3):286-98.
  32. The shorter zinc finger protein ZNF230 gene message is transcribed in fertile male testes and may be related to human spermatogenesis. Zhang S, Qiu W, Wu H, Zhang G, Huang M, Xiao C, Yang J, Kamp C, Huang X, Huellen K, Yue Y, Pan A, Lebo R, Milunsky A, Vogt PH. Biochem J. 2001 Nov 1;359(Pt 3):721-7.
  33. High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome. Kamp C, Huellen K, Fernandes S, Sousa M, Schlegel PN, Mielnik A, Kleiman S, Yavetz H, Krause W, Küpker W, Johannisson R, Schulze W, Weidner W, Barros A, Vogt PH. Mol Hum Reprod. 2001 Oct;7(10):987-94.
  34. Arylsulfatase D gene in Xp22.3 encodes two protein isoforms. Urbitsch P, Salzer MJ, Hirschmann P, Vogt PH. DNA Cell Biol. 2000 Dec;19(12):765-73.
  35. Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. Paracchini S, Stuppia L, Gatta V, Palka G, Moro E, Foresta C, Mengua L, Oliva R, Ballescà JL, Kremer JA, van Golde RJ, Tuerlings JH, Hargreave T, Ross A, Cooke H, Huellen K, Vogt PH, Tyler-Smith C. J Endocrinol Invest. 2000 Nov;23(10):671-6.
  36. Conservation of the deleted-in-azoospermia-like-1 (DAZL1) gene structure in old world monkeys points to a homologous function of DAZL1 in this primate class.Grossmann B, Weinbauer G, Hirschmann P, Vogt PH. J Endocrinol Invest. 2000 Oct;23(9):616-22.
  37. Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events. Kamp C, Hirschmann P, Voss H, Huellen K, Vogt PH. Hum Mol Genet. 2000 Oct 12;9(17):2563-72.
  38. Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions. Simoni M, Bakker E, Eurlings MC, Matthijs G, Moro E, Müller CR, Vogt PH. Int J Androl. 1999 Oct;22(5):292-9.
  39. Neurodegenerative diseases in children conceived by intracytoplasmic sperm injection?  Vogt PH. Lancet. 1999 Aug 21;354(9179):611-2. No abstract available.
  40. Human chromosome deletions in Yq11, AZF candidate genes and male infertility: history and update. Vogt PH. Mol Hum Reprod. 1998 Aug;4(8):739-44. Review.
  41. Genetics of idiopathic male infertility: Y chromosomal azoospermia factors (AZFa, AZFb, AZFc). Vogt PH. Baillieres Clin Obstet Gynaecol. 1997 Dec;11(4):773-95. Review.
  42. DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails. Habermann B, Mi HF, Edelmann A, Bohring C, Bäckert IT, Kiesewetter F, Aumüller G, Vogt PH. Hum Reprod. 1998 Feb;13(2):363-9.
  43. Multiplex PCR: critical parameters and step-by-step protocol. Henegariu O, Heerema NA, Dlouhy SR, Vance GH, Vogt PH. Biotechniques. 1997 Sep;23(3):504-11.
  44. Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm. Elliott DJ, Millar MR, Oghene K, Ross A, Kiesewetter F, Pryor J, McIntyre M, Hargreave TB, Saunders PT, Vogt PH, Chandley AC, Cooke H. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):3848-53.
  45. Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997. Vogt PH, Affara N, Davey P, Hammer M, Jobling MA, Lau YF, Mitchell M, Schempp W, Tyler-Smith C, Williams G, Yen P, Rappold GA. Cytogenet Cell Genet. 1997;79(1-2):1-20.
  46. Molecular basis of male (in)fertility. Vogt PH. Int J Androl. 1997;20 Suppl 3:2-10. Review.
  47. Human Y chromosome deletions in Yq11 and male fertility. Vogt PH. Adv Exp Med Biol. 1997;424:17-30. Review.
  48. A SPGY copy homologous to the mouse gene Dazla and the Drosophila gene boule is autosomal and expressed only in the human male gonad. Shan Z, Hirschmann P, Seebacher T, Edelmann A, Jauch A, Morell J, Urbitsch P, Vogt PH. Hum Mol Genet. 1996 Dec;5(12):2005-11.
  49. 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. Hum Mol Genet. 1996 Jul;5(7):933-43.
  50. Molecular analysis of the genomic structure of the human Y chromosome in the euchromatic part of its long arm (Yq11). Kirsch S, Keil R, Edelmann A, Henegariu O, Hirschmann P, LePaslier D, Vogt PH. Cytogenet Cell Genet. 1996;75(2-3):197-206.
  51. Genetic aspects of human infertility. Vogt PH. Int J Androl. 1995 Dec;18 Suppl 2:3-6. Review.
  52. Genetic aspects of artificial fertilization. Vogt PH. Hum Reprod. 1995 Oct;10 Suppl 1:128-37. Review.
  53. The azoospermia factor (AZF) of the human Y chromosome in Yq11: function and analysis in spermatogenesis. Vogt PH, Edelmann A, Hirschmann P, Köhler MR. Reprod Fertil Dev. 1995;7(4):685-93. Review.
  54. Interstitial deletions of repetitive DNA blocks in dicentric human Y chromosomes. Köhler MR, Vogt PH. Chromosoma. 1994 Sep;103(5):324-30.

 

Nicht Pubmed gelistet:

  1. Genetik des Premature-ovarian-failure-syndroms. Strowitzki T, Vogt PH Gynäkol. Endokrinologie (2003)1: 128-134.
  2. Genetische Ursachen der prämaturen Ovarialinsuffizienz. Dr. J. Rehnitz, T. Strowitzki, P. H. Vogt. Gynäkologische Endokrinologie;  Ausgabe: 4 / 2018
  3. Labordiagnostik bei prämaturer Ovarialinsuffizienz (POI).  Dr. Julia Rehnitz, Prof. Dr. Dr. h.c. Thomas Strowitzki; Der Gynäkologe; Ausgabe: online /2019
  4. Fehlanlage der Gonaden und endokrinologische Ursachen genitaler Fehlbildungen bei Frauen. Dr. P. Frank-Herrmann, P. Vogt, T. Strowitzki; Der Gynäkologe; Ausgabe: 02 /2016