P H Vogt

Summary

Affiliation: University of Heidelberg
Country: Germany

Publications

  1. ncbi request reprint Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997
    P H Vogt
    Institut fur Humangenetik, Universitat Heidelberg, Germany
    Cytogenet Cell Genet 79:1-20. 1997
  2. ncbi request reprint Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
    P H Vogt
    Section Molecular Human Genetics, University of Heidelberg, Germany
    Hum Mol Genet 5:933-43. 1996
  3. pmc A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N
    S Fernandes
    Section of Molecular Genetics and Infertility, Department of Gynecological Endocrinology and Reproductive Medicine, University of Heidelberg, Heidelberg, Germany
    Am J Hum Genet 74:180-7. 2004
  4. doi request reprint The AZF proteins
    P H Vogt
    Molecular Genetics and Infertility Unit, Department of Gynecology, Endocrinology and Infertility, University Women Hospital, Heidelberg, Germany
    Int J Androl 31:383-94. 2008
  5. ncbi request reprint Arylsulfatase D gene in Xp22.3 encodes two protein isoforms
    P Urbitsch
    Institute of Human Genetics, University of Heidelberg, INF 328, D 69120 Heidelberg, Germany
    DNA Cell Biol 19:765-73. 2000
  6. ncbi request reprint DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails
    B Habermann
    Department of Andrology, Centre of Dermatology, University of Marburg, Germany
    Hum Reprod 13:363-9. 1998
  7. pmc The shorter zinc finger protein ZNF230 gene message is transcribed in fertile male testes and may be related to human spermatogenesis
    S Zhang
    Department of Medical Genetics, West China Hospital and Key Laboratory of Morbid Genomics and Forensic Medicine of Sichuan, Sichuan University, Chengdu, Sichuan 610041, People s Republic of China
    Biochem J 359:721-7. 2001
  8. ncbi request reprint High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
    S Fernandes
    Reproduction Genetics, Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany
    Mol Hum Reprod 8:286-98. 2002
  9. ncbi request reprint A SPGY copy homologous to the mouse gene Dazla and the Drosophila gene boule is autosomal and expressed only in the human male gonad
    Z Shan
    Institute of Human Genetics, University of Heidelberg, Germany
    Hum Mol Genet 5:2005-11. 1996
  10. ncbi request reprint High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome
    C Kamp
    Reproduction Genetics, Institute of Human Genetics, University of Heidelberg, Im Neuenheimer Feld 328, D-69120 Heidelberg, Germany
    Mol Hum Reprod 7:987-94. 2001

Collaborators

  • M A Jobling
  • A Jung
  • Eberhard Nieschlag
  • F M Kohn
  • Walter Krause
  • Mario Sousa
  • Peter N Schlegel
  • Y Lau
  • S Fernandes
  • K Huellen
  • C Kamp
  • B Habermann
  • P Urbitsch
  • A Barros
  • S Zhang
  • P Hirschmann
  • S Paracchini
  • L H Meyer
  • C Tyler-Smith
  • G Floridia
  • A Edelmann
  • Z Shan
  • J Zeisler
  • H Dukal
  • J Goncalves
  • E Rajpert De Meyts
  • N E Skakkebaek
  • X Huang
  • A Milunsky
  • R Johannisson
  • A Pan
  • C Xiao
  • M Huang
  • H Yavetz
  • S Kleiman
  • W Schulze
  • G Zhang
  • R Lebo
  • W Weidner
  • J Yang
  • Y Yue
  • W Qiu
  • H Wu
  • A Mielnik
  • M J Salzer
  • G Aumuller
  • H F Mi
  • I T B├Ąckert
  • C Bohring
  • F Kiesewetter
  • T Seebacher
  • J Morell
  • A Jauch

Detail Information

Publications10

  1. ncbi request reprint Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997
    P H Vogt
    Institut fur Humangenetik, Universitat Heidelberg, Germany
    Cytogenet Cell Genet 79:1-20. 1997
  2. ncbi request reprint Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
    P H Vogt
    Section Molecular Human Genetics, University of Heidelberg, Germany
    Hum Mol Genet 5:933-43. 1996
    ..As the most severe phenotype after deletion of each locus is azoospermia, we designated them as: AZFa, AZFb and AZFc. Their probable phase of function in human spermatogenesis and candidate genes involved will be discussed...
  3. pmc A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N
    S Fernandes
    Section of Molecular Genetics and Infertility, Department of Gynecological Endocrinology and Reproductive Medicine, University of Heidelberg, Heidelberg, Germany
    Am J Hum Genet 74:180-7. 2004
    ..These data confirm the expectation that the human Y chromosome sequence and gene complement may differ substantially between individuals and more variations are to be expected in different Y chromosomal haplogroups...
  4. doi request reprint The AZF proteins
    P H Vogt
    Molecular Genetics and Infertility Unit, Department of Gynecology, Endocrinology and Infertility, University Women Hospital, Heidelberg, Germany
    Int J Androl 31:383-94. 2008
    ....
  5. ncbi request reprint Arylsulfatase D gene in Xp22.3 encodes two protein isoforms
    P Urbitsch
    Institute of Human Genetics, University of Heidelberg, INF 328, D 69120 Heidelberg, Germany
    DNA Cell Biol 19:765-73. 2000
    ....
  6. ncbi request reprint DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails
    B Habermann
    Department of Andrology, Centre of Dermatology, University of Marburg, Germany
    Hum Reprod 13:363-9. 1998
    ..Deletion of DAZ genes is supposed not to interfere with human sperm maturation but to result in a gradual reduction of mature spermatozoa...
  7. pmc The shorter zinc finger protein ZNF230 gene message is transcribed in fertile male testes and may be related to human spermatogenesis
    S Zhang
    Department of Medical Genetics, West China Hospital and Key Laboratory of Morbid Genomics and Forensic Medicine of Sichuan, Sichuan University, Chengdu, Sichuan 610041, People s Republic of China
    Biochem J 359:721-7. 2001
    ..The lack of detectable ZNF230 expression in azoospermic patients by reverse transcriptase-mediated PCR analysis is interpreted to mean that this gene is involved in maintaining normal human male fertility...
  8. ncbi request reprint High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
    S Fernandes
    Reproduction Genetics, Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany
    Mol Hum Reprod 8:286-98. 2002
    ..It is most likely caused by intrachromosomal recombination events between two long repetitive sequence blocks (AZFc-Rep1) flanking the DAZ gene structures...
  9. ncbi request reprint A SPGY copy homologous to the mouse gene Dazla and the Drosophila gene boule is autosomal and expressed only in the human male gonad
    Z Shan
    Institute of Human Genetics, University of Heidelberg, Germany
    Hum Mol Genet 5:2005-11. 1996
    ..SPGYLA encodes an RNA binding protein expressed only in the human male gonad. The data presented give strong evidence that not DAZ but SPGYLA is the functional human homologue of Dazla and boule...
  10. ncbi request reprint High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome
    C Kamp
    Reproduction Genetics, Institute of Human Genetics, University of Heidelberg, Im Neuenheimer Feld 328, D-69120 Heidelberg, Germany
    Mol Hum Reprod 7:987-94. 2001
    ..This may provide a valuable prognostic tool for infertility clinics performing testicular sperm extraction, as it would enable the exclusion of AZFa patients with a complete SCO syndrome...