Publications Jutta Wirth 2009 (30 Articles)
Wirth J. (2009). Beruflicher Erfolg mit langfristiger Perspektive: Gewusst wie in der Zellkulturtechnik. MTA-Dialog 5 (10), 24-25. URL: http://www.mta-dialog.de/suche.htm?phrase=Jutta%20Wirth
Wirth J. (2007). Zellkulturtechniken: Die verschiedenen Techniken für Zell- und Gewebekulturen als wichtigste Prüfmethoden in der Gesundheits- und Umweltmedizin. Newsletter Quartal IV.
Wirth J. (2007). Die Polymerase-Ketten-Reaktion (PCR). Isolierung, Amplifizierung und Detektion von Nukleinsäuren. Newsletter der Technischen Assistenten in der Medizin. Newsletter Quartal II.
Daniela Ehling, Ingo Kennerknecht, Annelore Junge, Bettina Prager, Rita Exeler, Beate Lemcke, Juergen Horst, Thomas Schmitt-John, Oliver Bartsch, J Wirth (2004). Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies. Am J Med Genet: 15;131(3):265-72.
Glaeser B, Shirneshan K, Bink K, Wirth J, Kehrer-Sawatzki H, Bartz U, Zoll B, Bohlander SK (2004). Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations. Am J Med Genet; 30;126(3):229-36.
Hertz JM, Sivertsen B, Silahtaroglu A, Bugge M, Kalscheuer V, Weber A, Wirth J, Ropers HH, Tommerup N, Tumer Z. (2004). Early onset, non-progressive, mild cerebellar ataxia co-segregating with a familial balanced translocation t(8;20)(p22;q13). J Med Genet; 41(3):e25.
2002-2001
Barbi G, Rossier E, Vossbeck S, Hummler H, Lang D, Flock F, Terinde R, Wirth J, Vogel W, Kehrer-Sawatzki H (2002). Constitutional de novo interstitial deletion of 8 Mb on chromosome 22q12.1-12.3 encompassing the neurofibromatosis type 2 (NF2) locus in a dysmorphic girl with severe malformations. J Med Genet; 39(2):E6.
Stankiewicz P, Brozek I, Helias-Rodzewicz Z, Wierzba J, Pilch J, Bocian E, Balcerska A, Wozniak A, Kardas I, Wirth J, Mazurczak T, Limon J. (2001). Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18. Am J Med Genet; 101(3) 226-39.
Naguib M, Hammerschmidt K, Wirth J. (2001). Microgeographic variation, habitat effects and individual signature cues in calls of chiffchaffs Phylloscopus collybita canarensis. Ethology; 107 (4): 341-355.
Nothwang HG, Kim HG, Aoki J, Geisterfer M, Kubart S, Wegner RD, van Moers A, Ashworth LK, Haaf T, Bell J, Arai H, Tommerup N, Ropers HH, Wirth J. (2001). Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain. Hum Mol Genet; 10(8):797-806.
Borck G, Wirth J, Hardt T, Tonnies H, Brondum-Nielsen K, Bugge M, Tommerup N, Nothwang HG, Ropers HH, Haaf T. (2001). Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome. J Med Genet; 38(2):117-21.
Zhu G, Gillessen-Kaesbach G, Wirth J, Passarge E, Bartsch O. (2001). Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2). Am J Med Genet; 98(4):317-9.
Wirth J, Back E, Huttenhofer A, Nothwang HG, Lich C, Gross S, Menzel C, Schinzel A, Kioschis P, Tommerup N, Ropers HH, Horsthemke B, Buiting K. (2001). A translocation breakpoint cluster disrupts the newly defined 3′ end of the SNURF-SNRPN transcription unit on chromosome 15. Hum Mol Genet; 10(3):201-10.
2000
Nothwang HG, Schroer A, van der Maarel S, Kubart S, Schneider S, Riesselmann L, Menzel C, Hinzmann B, Vogt D, Rosenthal A, Fryns J, Tommerup N, Haaf T, Ropers HH, Wirth J. (2000) Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations. Cytogenet Cell Genet; 90(1-2):126-33.
Kirchhoff M, Rose H, Maahr J, Gerdes T, Bugge M, Tommerup N, Tumer Z, Lespinasse J, Jensen PK, Wirth J, Lundsteen C. (2000). High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. Eur J Hum Genet; 8(9):661-8.
Vollmer M, Kremer M, Ruf R, Miot S, Nothwang HG, Wirth J, Otto E, Krapf R, Hildebrandt F. 2000 Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes. Genomics 2000; 68(2):127-35.
Heller A, Seidel J, Hubler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. (2000). Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review. J Med Genet; 37(7):529-32.
Scheer MP, van der Maarel S, Kubart S, Schulz A, Wirth J, Schweiger S, Ropers H, Nothwang HG. (2000). DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner. Genomics;63(1):123-32.
1994-1999
Stumm M, Koch A, Wieacker PF, Phillip C, Steinbach F, Allhoff EP, Buhtz P, Walter H, Tonnies H, Wirth J. (1999). Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma. Cancer Genet Cytogenet; 115(1):82-5.
Wirth J, Nothwang HG, van der Maarel S, Menzel C, Borck G, Lopez-Pajares I, Brondum-Nielsen K, Tommerup N, Bugge M, Ropers HH, Haaf T. (1999). Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes. J Med Genet; 36(4):271-8.
Silahtaroglu A, Hol FA, Jensen PK, Erdel M, Duba HC, Geurds MP, Knoers NV, Mariman EC, Tumer Z, Utermann G, Wirth J, Bugge M, Tommerup N. (1999). Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. Eur J Hum Genet; 7(1):68-76.
Caubit X, Thangarajah R, Theil T, Wirth J, Nothwang HG, Ruther U, Krauss S. (1999). Mouse Dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud. Dev Dyn;214(1):66-80.
Duba HC, Erdel M, Loffler J, Wirth J, Utermann B, Utermann G. (1998). Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier. Eur J Hum Genet; 6(1):75-9.
Silahtaroglu AN, Hacihanefioglu S, Guven GS, Cenani A, Wirth J, Tommerup N, Tumer Z. (1998). Not para-, not peri-, but centric inversion of chromosome 12. J Med Genet;35(8):682-4.
Nothwang HG, Wirth J, Brandl B, Haaf T, Nielsen KB, Tommerup N, Ropers HH. (1997). Identification of positional candidates for neurological disorders on chromsome 13q14–>q22. Cytogenet Cell Genet; 79(3-4):293-7.
Kingsley K, Wirth J, van der Maarel S, Freier S, Ropers HH, Haaf T. (1997). Complex FISH probes for the subtelomeric regions of all human chromosomes: comparative hybridization of CEPH YACs to chromosomes of the Old World monkey Presbytis cristata and great apes. Cytogenet Cell Genet; 78(1):12-9.
Wagner T, Tommerup N, Wirth J, Leffers H, Zimmer J, Back E, Weissenbach J, Scherer G. (1997). A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3. Cytogenet Cell Genet; 76(3-4):172-5.
Wirth J, Wagner T, Meyer J, Pfeiffer RA, Tietze HU, Schempp W, Scherer G. (1996). Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9. Hum Genet; 97(2):186-93.
Meyer J, Wirth J, Held M, Schempp W, Scherer G. (1996). SOX20, a new member of the SOX gene family, is located on chromosome 17p13. Cytogenet Cell Genet; 72(2-3):246-9.
Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, et al. (1994). Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell; 79(6):1111-20.
Professional articles
Wirth, J. (2008). Was juckt denn da? Allergien – steckt unser Abwehrsystem in der Krise? Volkshochschule Lemgo, VHS.
Wirth, J. (2008). Gentechnologie „ Ganz obanan auf der Speiskarte. Volkshochschule Lemgo, VHS 2008.
Wirth, J. (2008). Was juckt denn da? Allergien – steckt unser Abwehrsystem in der Krise? Volkshochschule Lemgo, VHS 2008.
Wirth, J. (20087. Im Mittelpunkt „Gentechnik für den Menschen „Volkshochschule Lemgo, VHS 2007.
Wirth, J. (2007). Vogelgrippe- oder Geflügelpest – eine Tierseuche und ihre Infektionswege. Volkshochschule Lemgo, VHS 2007.
Wirth, J. (2006). Gentechnik – Segen oder Plage. Volkshochschule Lemgo, VHS 2006.
Wirth, J. (2006). Fit durch den Winter? Abwehrkräfte des Körpers besiegen eine Grippe und andere herkömmliche Erkältungen. Was bewirken Impfstoffe dabei. Volkshochschule Lemgo, VHS.
Publications 2010-2015, read here…
