Draft:Peter Michael Lansdorp

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  • Comment: As before. Drmies (talk) 01:48, 27 March 2024 (UTC)
  • Comment: This draft is better, but there are still too many peacock terms. In addition, currently this lists his research but really does not prove that he is notable. That needs recognition by others. For instance senior fellow of major societies, major awards (not grants). Please read WP:NPROF carefully.
    Also, the long list of his research ares is not useful unless they are quoted in a major awards. This is not the place for a CV. Ldm1954 (talk) 14:00, 5 January 2024 (UTC)
  • Comment: Uses WP:PEACOCK terms on multiple instances, especially to describe the subject of the submission. Eternal Shadow Talk 22:51, 31 December 2023 (UTC)

Peter Michael Lansdorp (born December 16, 1952) is recognized for his contributions in the fields of hematology, medical genetics and cancer research. He has made significant contributions to the understanding of genome instability, particularly in relation to aging and cancer. His research has focused on the biology of blood-forming stem cells, telomeres and genome analysis. He is also known for the development of techniques including single cell Strand-seq and fluorescence in situ hybridization (FISH) techniques such as Q-FISH and flow FISH.[1]

Early Life & Career[edit]

Peter Lansdorp grew up in the Netherlands (Den Haag and Wassenaar). He obtained a Medical Degree from the Erasmus University in Rotterdam in 1976.[1] His early career included work on monoclonal antibodies at Sanquin and he obtained a PhD from the University of Amsterdam in 1985.[citation needed] Between 2011 and 2017, he was the Founding Scientific Director of the European Research Institute for the Biology of Aging at the University of Groningen, the Netherlands. He returned to Vancouver in 2017, resuming his role as a Distinguished Scientist at the Terry Fox Laboratory and a Professor in Hematology and Medical Genetics at the University of British Columbia.[2][3]

Research[edit]

In 1984, Lansdorp made a significant contribution to the field of monoclonal antibodies with the discovery of a method to efficiently form bifunctional tetrameric antibody complexes.[citation needed] This method was patented and later licensed to StemCell Technologies in Vancouver.[4] Lansdorp's early work in Vancouver predominantly focused on experimental hematology. He first demonstrated that the functional properties of purified "candidate" blood forming stem cells, including their self-renewal properties, change dramatically during development.[citation needed] He subsequently showed that telomere repeats are lost in purified hematopoietic stem cells supporting the concept that blood stem cells do not truly "self-renew" but are mortal like most other somatic cells.[citation needed]

Lansdorp also developed a novel fluorescent in situ hybridization (FISH) method to measure the length of telomere repeats using peptide nucleic acid (PNA) probes.[citation needed] He subsequently showed that flow cytometry can be used to measure the average telomere length in individual nucleated blood cells.[citation needed]

In 2002 Lansdorp provided compelling evidence for the formation of guanine quadruplex (G4) DNA structures in C. elegans.[citation needed] He proposed that the dog-1 helicase gene is required to unwind G4 DNA structures that occasionally form during DNA synthesis.[citation needed]

External Links[edit]

References[edit]

  1. ^ a b "» Peter Lansdorp". neuroscience.umcg.nl. Retrieved 2023-12-31.
  2. ^ "macgenome.org" (PDF).
  3. ^ "open.library.ubc.ca".
  4. ^ US4868109A, Lansdorp, Peter M., "Immunological antibody complex, its preparation and its use", issued 1989-09-19