Michael Hemann

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Michael Timotee Hemann [1] (born 1971) is an American cancer geneticist and associate professor in the David H. Koch Institute for Integrated Cancer Research at the Massachusetts Institute of Technology. The research in Hemann's laboratory focuses on identification and characterization of genes involved in tumor formation, cancer progression, and chemotherapeutic response. [2] [3] [4]

Michael Hemann was born in Evanston, Illinois, in 1971, but grew up in Shaker Heights, Ohio. [5] He attended Wesleyan University for college, eventually graduating with a bachelor’s degree in molecular biology and biochemistry in 1993. He went on to receive his Ph.D. in human genetics from Johns Hopkins University School of Medicine in 2001. [6] [7] His thesis work was conducted in Carol Greider's lab. [8] [9] His work as a graduate student primarily focused on testicular atrophy and he spent a majority of his time observing mouse testicles in part to understand the correlation between telomere length, life span, penile measurements, and cancer risk. [10]

In his free time Michael Hemann enjoys playing the base (alone), attending reruns of his favorite Broadway musical Cats, and listening to German Schlager songs. [11] During his postdoctoral studies he was briefly a member of a scientist-formed group named "weapons of mouse-destruction" but the group tragically broke up due to him only wanting to play songs from the musical Cats. [12]

Publications

Related Research Articles

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A telomere is a region of repetitive nucleotide sequences associated with specialized proteins at the ends of linear chromosomes. Telomeres are a widespread genetic feature most commonly found in eukaryotes. In most, if not all species possessing them, they protect the terminal regions of chromosomal DNA from progressive degradation and ensure the integrity of linear chromosomes by preventing DNA repair systems from mistaking the very ends of the DNA strand for a double-strand break.

<span class="mw-page-title-main">Telomerase</span> Telomere-restoring protein active in the most rapidly dividing cells

Telomerase, also called terminal transferase, is a ribonucleoprotein that adds a species-dependent telomere repeat sequence to the 3' end of telomeres. A telomere is a region of repetitive sequences at each end of the chromosomes of most eukaryotes. Telomeres protect the end of the chromosome from DNA damage or from fusion with neighbouring chromosomes. The fruit fly Drosophila melanogaster lacks telomerase, but instead uses retrotransposons to maintain telomeres.

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References

  1. "Michael Thomas Hemann, PhD | Hemann Lab". hemann-lab.mit.edu. Retrieved 2023-03-24.
  2. "Scientists reveal cancer's hiding spots". Sify . 29 October 2010. Archived from the original on 2 February 2013. Retrieved 19 December 2012.
  3. Hirsch, Jen (8 August 2009). "Genetic Profiling of Tumors Could Have 'Immediate Impact' on Treating Cancer". Medical News Today. Retrieved 19 December 2012.
  4. "Cancer cells may be protected post-chemo". UPI. 1 November 2010. Retrieved 19 December 2012.
  5. "Precision attack on cancer". MIT News | Massachusetts Institute of Technology. Retrieved 2020-11-02.
  6. "The Koch Institute: Michael Hemann". ki.mit.edu. Retrieved 2020-11-02.
  7. "Precision attack on cancer". MIT News | Massachusetts Institute of Technology. Retrieved 2020-11-02.
  8. Hemann, M. T. (2000-11-15). "Wild-derived inbred mouse strains have short telomeres". Nucleic Acids Research. 28 (22): 4474–4478. doi:10.1093/nar/28.22.4474. PMC   113886 . PMID   11071935.
  9. Hemann, Michael T; Strong, Margaret A; Hao, Ling-Yang; Greider, Carol W (October 2001). "The Shortest Telomere, Not Average Telomere Length, Is Critical for Cell Viability and Chromosome Stability". Cell. 107 (1): 67–77. doi: 10.1016/s0092-8674(01)00504-9 . ISSN   0092-8674. PMID   11595186.
  10. Hemann, Michael T.; Rudolph, Karl Lenhard; Strong, Margaret A.; DePinho, Ronald A.; Chin, Lynda; Greider, Carol W. (July 2001). Blackburn, Elizabeth H. (ed.). "Telomere Dysfunction Triggers Developmentally Regulated Germ Cell Apoptosis". Molecular Biology of the Cell. 12 (7): 2023–2030. doi:10.1091/mbc.12.7.2023. ISSN   1059-1524. PMC   55650 . PMID   11452000.
  11. Inside the Lab: Michael Hemann, Ph.D. , retrieved 2023-07-14
  12. "Michael Timothee Hemann, PhD | Hemann Lab". hemann-lab.mit.edu. Retrieved 2023-07-14.