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  • Bergman, AnnikaGothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology,Lundberg Laboratory for Cancer Research, Department of Pathology, The Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden (författare)

Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer

  • Artikel/kapitelEngelska2009

Förlag, utgivningsår, omfång ...

  • 2009-10-28
  • Taylor & Francis,2009
  • printrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:hj-39619
  • https://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-39619URI
  • https://doi.org/10.3109/02844310903247228DOI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-27712URI
  • https://gup.ub.gu.se/publication/132011URI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:119689831URI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:art swepub-publicationtype

Anmärkningar

  • Saethre-Chotzen syndrome is one of the most common craniosynostosis syndromes. It is an autosomal dominantly inherited disorder with variable expression that is caused by germline mutations in the TWIST1 gene or more rarely in the FGFR2 or FGFR3 genes. We have previously reported that patients with Saethre-Chotzen syndrome have an increased risk of developing breast cancer. Here we have analysed a cohort of 26 women with BRCA1/2-negative hereditary breast cancer to study whether a proportion of these families might have mutations in Saethre-Chotzen-associated genes. DNA sequence analysis of TWIST1 showed no pathogenic mutations in the coding sequence in any of the 26 patients. MLPA (multiplex ligation-dependent probe amplification)-analysis also showed no alterations in copy numbers in any of the craniofacial disorder genes MSX2, ALX4, RUNX2, EFNB1, TWIST1, FGFR1, FGFR2,FGFR3, or FGFR4. Taken together, our findings indicate that mutations in Saethre-Chotzen-associated genes are uncommon or absent in BRCA1/2-negative patients with hereditary breast cancer.

Ämnesord och genrebeteckningar

  • MEDICIN OCH HÄLSOVETENSKAP Klinisk medicin Kirurgi hsv//swe
  • MEDICAL AND HEALTH SCIENCES Clinical Medicine Surgery hsv//eng
  • MEDICIN OCH HÄLSOVETENSKAP Klinisk medicin Cancer och onkologi hsv//swe
  • MEDICAL AND HEALTH SCIENCES Clinical Medicine Cancer and Oncology hsv//eng
  • MEDICIN OCH HÄLSOVETENSKAP Medicinska och farmaceutiska grundvetenskaper Cell- och molekylärbiologi hsv//swe
  • MEDICAL AND HEALTH SCIENCES Basic Medicine Cell and Molecular Biology hsv//eng
  • BRCA1
  • BRCA2
  • FGFR2
  • FGFR3
  • Hereditary breast cancer
  • Saethre-Chotzen syndrome
  • TWIST1
  • ALX4 protein
  • human
  • DNA binding protein
  • EFNB1 protein
  • human
  • ephrin B1
  • FGFR1 protein
  • human
  • FGFR2 protein
  • human
  • FGFR3 protein
  • human
  • FGFR4 protein
  • human
  • fibroblast growth factor receptor 1
  • fibroblast growth factor receptor 2
  • fibroblast growth factor receptor 3
  • fibroblast growth factor receptor 4
  • homeodomain protein
  • nuclear protein
  • RUNX2 protein
  • human
  • transcription factor
  • transcription factor MSX2
  • transcription factor RUNX2
  • transcription factor Twist
  • TWIST1 protein
  • human
  • acrocephalosyndactyly
  • adult
  • article
  • breast tumor
  • DNA sequence
  • female
  • genetic screening
  • genetics
  • human
  • middle aged
  • mutation
  • polymerase chain reaction
  • tumor suppressor gene
  • Acrocephalosyndactylia
  • Breast Neoplasms
  • Core Binding Factor Alpha 1 Subunit
  • DNA-Binding Proteins
  • Ephrin-B1
  • Genes
  • BRCA1
  • Genes
  • BRCA2
  • Genetic Testing
  • Germ-Line Mutation
  • Homeodomain Proteins
  • Humans
  • Nuclear Proteins
  • Receptor
  • Fibroblast Growth Factor
  • Type 1
  • Receptor
  • Fibroblast Growth Factor
  • Type 2
  • Receptor
  • Fibroblast Growth Factor
  • Type 3
  • Receptor
  • Fibroblast Growth Factor
  • Type 4
  • Sequence Analysis
  • DNA
  • Transcription Factors
  • Twist Transcription Factor
  • Acrocephalosyndactylia
  • epidemiology
  • genetics
  • Adult
  • Breast Neoplasms
  • Core Binding Factor Alpha 1 Subunit
  • DNA-Binding Proteins
  • Ephrin-B1
  • Female
  • Genes
  • BRCA1
  • BRCA2
  • Genetic Testing
  • Germ-Line Mutation
  • Homeodomain Proteins
  • Humans
  • Middle Aged
  • Nuclear Proteins
  • Polymerase Chain Reaction
  • Receptor
  • Fibroblast Growth Factor
  • Type 1
  • Type 2
  • Type 3
  • Type 4
  • Sequence Analysis
  • DNA
  • Transcription Factors
  • Twist Transcription Factor

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Sahlin, PelleGothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,Department of Plastic Surgery, The Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden(Swepub:gu)xsahpe (författare)
  • Emanuelsson, MonicaUmeå universitet,Onkologi,Oncology Center, Umeå University Hospital, Umeå, Sweden(Swepub:umu)moem0001 (författare)
  • Carén, Helena,1979Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,Department of Clinical Genetics, The Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden(Swepub:gu)xcareh (författare)
  • Tarnow, Peter,1963Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institutionen för kliniska vetenskaper, Avdelningen för plastikkirurgi,Institute of Clinical Sciences,Institute of Clinical Sciences, Department of Plastic Surgery,Department of Plastic Surgery, The Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden(Swepub:gu)xtarpe (författare)
  • Martinsson, Tommy,1956Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics,Department of Clinical Genetics, The Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden(Swepub:gu)xmarto (författare)
  • Grönberg, HenrikKarolinska Institutet,Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden (författare)
  • Stenman, Göran,1953Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology,Lundberg Laboratory for Cancer Research, Department of Pathology, The Sahlgrenska Academy at the University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden(Swepub:gu)xsteng (författare)
  • Göteborgs universitetInstitutionen för biomedicin, avdelningen för patologi (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery: Taylor & Francis43:5, s. 251-2550284-43111651-2073

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