Author Engel, Wolfgang

1 to 20 of 151 Items
  • 1978 Journal Article
    ​ ​Main Aspects of Geosynclinal Sedimentation in the Rhenohercynian Zone​
    Franke, W.; Eder, W.; Engel, W. & Langenstrassen, F. ​ (1978) 
    Zeitschrift der Deutschen Geologischen Gesellschaft129(1) pp. 201​-216​.​ DOI: https://doi.org/10.1127/zdgg/129/1978/201 
    Details  DOI 
  • 2000 Conference Abstract
    ​ ​Molecular approaches to the analysis of male infertility​
    Nayernia, K.; Shamsadin, R.; Adham, I. M. & Engel, W.​ (2000)
    Human Reproduction15 pp. 184​-185. 
    Oxford​: Oxford Univ Press.
    Details  WoS 
  • 2000 Journal Article
    ​ ​The relevance of chromosomal aberrations in male infertility​
    Pauer, H. U. & Engel, W.​ (2000) 
    GYNAKOLOGE33(2) pp. 88​-93​.​ DOI: https://doi.org/10.1007/s001290050016 
    Details  DOI  WoS 
  • 2000 Journal Article
    ​ ​Immortalization of murine male germ cells at a discrete stage of differentiation by a novel directed promoter-based selection strategy​
    Tascou, S.; Nayernia, K.; Samani, A.; Schmidtke, J.; Vogel, T.; Engel, W. & Burfeind, P.​ (2000) 
    Biology of Reproduction63(5) pp. 1555​-1561​.​ DOI: https://doi.org/10.1095/biolreprod63.5.1555 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Meiotic nondisjunction of chromosomes 1, 17, 18, X, and Y in men more than 80 years of age​
    Guttenbach, M.; Kohn, F. M.; Engel, W. & Schmid, M.​ (2000) 
    Biology of Reproduction63(6) pp. 1727​-1729​.​ DOI: https://doi.org/10.1095/biolreprod63.6.1727 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​The role of the testicular factor INSL3 in establishing the gonadal position​
    Adham, I. M.; Emmen, J. & Engel, W.​ (2000) 
    Molecular and Cellular Endocrinology160(1-2) pp. 11​-16​.​ DOI: https://doi.org/10.1016/S0303-7207(99)00188-4 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Genomic cloning, chromosomal mapping, and expression analysis Msal-2​
    Kohlhase, J.; Altmann, M.; Archangelo, L.; Dixkens, C. & Engel, W.​ (2000) 
    Mammalian Genome11(1) pp. 64​-68​.​ DOI: https://doi.org/10.1007/s003350010012 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Molecular cloning, expression and chromosome location of the human pelota gene PELO​
    Shamsadin, R.; Adham, I. M.; von Beust, G. & Engel, W.​ (2000) 
    CYTOGENETICS AND CELL GENETICS90(1-2) pp. 75​-78​.​ DOI: https://doi.org/10.1159/000015667 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article | Letter Note
    ​ ​Three novel SALL1 mutations extend the mutational spectrum in Townes-Brocks syndrome​
    Blanck, C.; Kohlhase, J.; Engels, P.; Burfeind, P.; Engel, W.; Bottani, A. & Patel, M. S. et al.​ (2000) 
    Journal of Medical Genetics37(4) pp. 303​-307​.​ DOI: https://doi.org/10.1136/jmg.37.4.303 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Hormonal control of gubernaculum development during testis descent: Gubernaculum outgrowth in vitro requires both insulin-like factor and androgen​
    Emmen, J.; McLuskey, A.; Adham, I. M.; Engel, W.; Grootegoed, J. A. & Brinkmann, A. O.​ (2000) 
    Endocrinology141(12) pp. 4720​-4727​.​ DOI: https://doi.org/10.1210/en.141.12.4720 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients​
    Huppke, P.; Laccone, F. A.; Kramer, N.; Engel, W. & Hanefeld, F.​ (2000) 
    Human Molecular Genetics9(9) pp. 1369​-1375​.​ DOI: https://doi.org/10.1093/hmg/9.9.1369 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Involvement of insulin-like factor 3 (Insl3) in diethylstilbestrol-induced cryptorchidism​
    Emmen, J.; Mcluskey, A.; Adham, I. M.; Engel, W.; Verhoef-Post, M.; Themmen, A. & Grootegoed, J. A. et al.​ (2000) 
    Endocrinology141(2) pp. 846​-849​.​ DOI: https://doi.org/10.1210/en.141.2.846 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Isolation and characterization of a novel human gene, NIF3L1,and its mouse ortholog, Nif3/1, highly conserved from bacteria to mammals​
    Tascou, S.; Uedelhoven, J.; Dixkens, C.; Nayernia, K.; Engel, W. & Burfeind, P.​ (2000) 
    CYTOGENETICS AND CELL GENETICS90(3-4) pp. 330​-336​.​ DOI: https://doi.org/10.1159/000056799 
    Details  DOI  PMID  PMC  WoS 
  • 2000 Journal Article
    ​ ​Alternative splicing, chromosome assignment and subcellular localization of the testicular haploid expressed gene (THEG)​
    Mannan, A. U.; Lucke, K.; Dixkens, C.; Neesen, J.; Kamper, M.; Engel, W. & Burfeind, P.​ (2000) 
    CYTOGENETICS AND CELL GENETICS91(1-4) pp. 171​-179​.​ DOI: https://doi.org/10.1159/000056840 
    Details  DOI  PMID  PMC  WoS 
  • 2001 Journal Article
    ​ ​Interactions between mouse ZP2 glycoprotein and proacrosin; a mechanism for secondary binding of sperm to the zona pellucida during fertilization​
    Howes, E.; Pascall, J. C.; Engel, W. & Jones, R.​ (2001) 
    Journal of Cell Science114(22) pp. 4127​-4136​.​
    Details  PMID  PMC  WoS 
  • 2001 Journal Article
    ​ ​Isolation and characterization of differentially expressed genes in invasive and non-invasive immortalized murine male germ cells in vitro​
    Tascou, S.; Nayernia, K.; Uedelhoven, J.; Bohm, D.; Jalal, R.; Ahmed, M. & Engel, W. et al.​ (2001) 
    International Journal of Oncology18(3) pp. 567​-574​.​
    Details  PMID  PMC  WoS 
  • 2001 Conference Abstract
    ​ ​The role of acrosin in combined infertility​
    Nayernia, K.; Adham, I. M.; Shamsadin, R. & Engel, W.​ (2001)
    Human Reproduction16 
    Oxford​: Oxford Univ Press.
    Details  WoS 
  • 2001 Journal Article | 
    ​ ​Human cyritestin genes (CYRN1 and CYRN2) are non-functional Pawel GRZMIL ,​
    Grzmil, P.; Kim, Y.; Shamsadin, R.; Neesen, J.; Adham, I. M.; Heinlein, U. A. O. & Schwarzer, U. J. et al.​ (2001) 
    Biochemical Journal375 pp. 551​-556​.​
    Details 
  • 2001 Journal Article
    ​ ​Human cyritestin genes (CYRN1 and CYRN2) are non-functional​
    Grzmil, P.; Kim, Y.; Shamsadin, R.; Neesen, A.; Adham, I. M.; Heinlein, U. & Schwarzer, U. J. et al.​ (2001) 
    Biochemical Journal357 pp. 551​-556​.​ DOI: https://doi.org/10.1042/0264-6021:3570551 
    Details  DOI  PMID  PMC  WoS 
  • 2001 Journal Article
    ​ ​MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin​
    Trappe, R.; Laccone, F. A.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F. & Engel, W.​ (2001) 
    The American Journal of Human Genetics68(5) pp. 1093​-1101​.​ DOI: https://doi.org/10.1086/320109 
    Details  DOI  PMID  PMC  WoS 

Researcher

Sort

issue date

ASC DESC

Items per Page