Ruth Mikelsaar

Summary

Affiliation: Institute of General and molecular Pathology, University of Tartu
Location: Tartu, Estonia
Publications:
Alpha-1 antitrypsin phenotypes in patients with Klinefelters syndrome. 2010,89(4),485-488. Journal of Genetics

Publications

  1. pmc Epitope of titin A-band-specific monoclonal antibody Tit1 5 H1.1 is highly conserved in several Fn3 domains of the titin molecule. Centriole staining in human, mouse and zebrafish cells
    Aavo Valdur Mikelsaar
    Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Cell Div 7:21. 2012
  2. doi request reprint Titin A-band-specific monoclonal antibody Tit1 5H1.1. Cellular Titin as a centriolar protein in non-muscle cells
    Aavo Valdur Mikelsaar
    Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Hybridoma (Larchmt) 29:391-401. 2010
  3. ncbi request reprint Reciprocal translocation t(7;16)(q21.2;p13.3) in an infertile man
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Fertil Steril 86:719.e9-11. 2006
  4. ncbi request reprint Chromosome variant 1qh- and its influence on the 3D organization of chromosome 1 heterochromatin in interphase nucleus of patients with endometriosis.
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila Street 19, Tartu 50411, Estonia
    J Genet 93:219-23. 2014
  5. ncbi request reprint Two novel deletions (array CGH findings) in pigment dispersion syndrome
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Ophthalmic Genet 28:216-9. 2007
  6. doi request reprint Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    J Appl Genet 52:331-4. 2011
  7. doi request reprint Balanced reciprocal translocation t(5;13)(q33;q12) and 9q31.1 microduplication in a man suffering from infertility and pollinosis
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Ravila 19, Tartu, Estonia
    J Appl Genet 53:93-7. 2012

Collaborators

  • O Bartsch
  • Aavo Valdur Mikelsaar
  • Anu Kõiveer
  • Peeter Toomik
  • Alar Sünter
  • Erkki Juronen
  • Imre Mikelsaar
  • Ingrid Kalev
  • Kalmer Karpson
  • Andres Piirsoo

Detail Information

Publications7

  1. pmc Epitope of titin A-band-specific monoclonal antibody Tit1 5 H1.1 is highly conserved in several Fn3 domains of the titin molecule. Centriole staining in human, mouse and zebrafish cells
    Aavo Valdur Mikelsaar
    Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Cell Div 7:21. 2012
    ..In this report we have studied the evolutionary aspects of the binding of MAb Tit1 5 H1.1 with its target antigen (titin)...
  2. doi request reprint Titin A-band-specific monoclonal antibody Tit1 5H1.1. Cellular Titin as a centriolar protein in non-muscle cells
    Aavo Valdur Mikelsaar
    Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Hybridoma (Larchmt) 29:391-401. 2010
    ..We suggest this anti-titin monoclonal antibody could be a valuable tool in the study of titin function and its subcellular location, both in muscle and non-muscle cells...
  3. ncbi request reprint Reciprocal translocation t(7;16)(q21.2;p13.3) in an infertile man
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Fertil Steril 86:719.e9-11. 2006
    ..To report the first case of reciprocal translocation t(7;16)(q21.2;p13.3) associated with male factor infertility...
  4. ncbi request reprint Chromosome variant 1qh- and its influence on the 3D organization of chromosome 1 heterochromatin in interphase nucleus of patients with endometriosis.
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of Biomedicine and Translational Medicine, University of Tartu, Ravila Street 19, Tartu 50411, Estonia
    J Genet 93:219-23. 2014
  5. ncbi request reprint Two novel deletions (array CGH findings) in pigment dispersion syndrome
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    Ophthalmic Genet 28:216-9. 2007
    ..We report the first male with pigment dispersion syndrome and a balanced translocation t(10;15)(p11.1;q11.1)...
  6. doi request reprint Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia
    J Appl Genet 52:331-4. 2011
    ..1 and/or fourfold dosage of centromeric/pericentromeric sequences of the chromosome 22 may be the cause of hypogonadotropic hypogonadism resulting in impaired spermatogenesis and infertility in our patient...
  7. doi request reprint Balanced reciprocal translocation t(5;13)(q33;q12) and 9q31.1 microduplication in a man suffering from infertility and pollinosis
    Ruth Mikelsaar
    Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Ravila 19, Tartu, Estonia
    J Appl Genet 53:93-7. 2012
    ..Single-nucleotide polymorphism (SNP) array analysis revealed a novel 9q31.1 microduplication inherited from both parents, which contributes to the genomic instability...