Sylvia Lawler

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Sylvia Dorothy Lawler
Born
Sylvia Dorothy Corben

(1922-01-15)January 15, 1922
Bournemouth, England
DiedJanuary 17, 1996(1996-01-17) (aged 74)
NationalityEnglish
Other namesSylvia Dorothy Bagshawe
Known forGenetics, Research into leukaemia and trophoblastic disease

Sylvia Dorothy Lawler (née Corben; 1922–1996) and later remarried as Sylvia Dorothy Bagshawe, was an English geneticist who worked in the field of human genetics.

Lawler was born and raised in Bournemouth, England, the only child of a furniture salesman and a schoolteacher.[1] She went on the study medicine at the University College London in 1939, distinguishing herself and graduating as the gold medalist of her year in 1945. She married Lawrence John Lawler who was captain in the Royal Electrical and Mechanical Engineers (REME); he later became a schoolteacher. They had one son, Anthony John born in 1955.[1]

Lawler's first marriage was dissolved in 1976, and on 28 January 1977 she married Kenneth Dawson Bagshawe, professor of medical oncology in the University of London, and son of Harry Bagshawe. Lawler died on 17 January 1996.[1]

Career[edit]

She began her work on the newly discovered rhesus blood-group system, and in 1949 she was invited to join the world's first department for the study of human genetics at Galton Laboratory at University College, London.[1] She went on to publish a book entitled Human Blood Groups and Inheritance in 1963.[2][3] Other publications during this period included A Genetical Study of the Gm Groups in Human Serum in 1960[4] and A pedigree showing some rare Rh genotypes[5]

Lawler was appointed as research scientist at the Institute of Cancer Research in London in 1960 and became the institute's first female professor in 1980. There she developed a broad interest in the genetics of malignancy. she made major contributions to the development of these tissue-typing techniques. Lawler laid the scientific foundation for work in bone-marrow transplantation and became chairman of the transplantation immunology subcommittee of the National Organ-Matching Service. She was a founder member of the International Workshops on Chromosomes in Leukaemia, and also established the first national fetal tissue bank in the UK, with support from the Medical Research Council.[1]

Publications[edit]

During Lawler's career she published a wide variety of journal articles, including Leukaemia;[6] The relation of parental sex and age to recombination in the HL-A system;[7] Cost of bone-marrow transplants in acute myeloid leukaemia;[8] Fetal tissue typing;[9] Genetic studies of complete and partial hydatidiform moles;[10] Histocompatibility antigens in asthma: population and family studies,[11] and Chromosomal damage and hair dyes.[12]

Scientific interests[edit]

A principal interest was in the genetic basis of trophoblastic disease, which encompasses molar pregnancies (hydatidiform moles) and choriocarcinoma, and in efforts to improve the diagnosis and treatment of this disease.[13][14] Lawler's work on histocompatibility leukocyte antigens (HLA antibodies) provided evidence that choriocarcinomas may arise from an earlier rather than simply the antecedent pregnancy. She went on to use genetic polymorphisms to determine the origins of complete and partial hydatidiform moles.[15] Lawler was also a pioneer in the analysis of the human genome. She was a foundation member and fellow of the Royal College of Pathologists and an honorary fellow of the Royal College of Physicians.[1]

Awards[edit]

Lawler's lifetime work was recognised in the form of the Royal Society of Medicine Syliver Lawler prize, each year two prizes are offered for the best scientific paper and the best clinical paper. Abstracts from scientists and clinicians in training on a clinical or basic scientific research project, and a panel of judges determine the best oral presentation.[16] It is highly competitive and well recognised award in the field of oncology.

References[edit]

  1. ^ a b c d e f Edwards, J. H.; Buckle, Veronica J. (23 September 2004). "Lawler [née Corben; other married name Bagshawe], Sylvia Dorothy (1922–1996), human geneticist". Oxford Dictionary of National Biography. Oxford University Press. 1. doi:10.1093/ref:odnb/60757.
  2. ^ Amazon entry for Human Blood Groups and Inheritance. ASIN 043561536X.
  3. ^ Lawler, Sylvia D.; Lawler, Lawrence J. (1966). Google Books copy of Human Blood Groups and Inheritance.
  4. ^ Lawler, Sylvia (January 1960). "A Genetical Study of the Gm Groups in Human Serum". Immunology. 1. 3: 90–94. PMC 1423994. PMID 14414701.
  5. ^ LAWLER, SD; BERTINSHAW, D (June 1949). "A pedigree showing some rare Rh genotypes". Annals of Eugenics. 14 (4): 285. PMID 18132301.
  6. ^ Lawler, SD (November 1972). "Leukaemia". Journal of Clinical Pathology. 25 (11): 1008. doi:10.1136/jcp.25.11.1008-a. PMC 477602. PMID 4265193.
  7. ^ Weitkamp, LR; Van Rood, JJ; Thorsby, E; Bias, W; Fotino, M; Lawler, SD; Dausset, J; Mayr, WR; Bodmer, J; Ward, FE; Seignalet, J; Payne, R; Kissmeyer-Nielsen, F; Gatti, RA; Sachs, JA; Lamm, LU (1973). "The relation of parental sex and age to recombination in the HL-A system". Human Heredity. 23 (3): 197–205. doi:10.1159/000152574. PMID 4760577.
  8. ^ Kay, HE; Powles, RL; Lawler, SD; Clink, HM (May 17, 1980). "Cost of bone-marrow transplants in acute myeloid leukaemia". Lancet. 1 (8177): 1067–9. doi:10.1016/s0140-6736(80)91508-1. PMID 6103400.
  9. ^ Singh, SP; Vyramuthu, N; Margoles, C; Lawler, SD (March 1980). "Fetal tissue typing". Indian Journal of Experimental Biology. 18 (3): 285–6. PMID 7390562.
  10. ^ Lawler, SD; Pickthall, VJ; Fisher, RA; Povey, S; Evans, MW; Szulman, AE (Sep 15, 1979). "Genetic studies of complete and partial hydatidiform moles". Lancet. 2 (8142): 580. doi:10.1016/s0140-6736(79)91632-5. PMID 89576.
  11. ^ Turton, CW; Morris, L; Buckingham, JA; Lawler, SD; Turner-Warwick, M (October 1979). "Histocompatibility antigens in asthma: population and family studies". Thorax. 34 (5): 670–6. doi:10.1136/thx.34.5.670. PMC 471146. PMID 515989.
  12. ^ Kirkland, DJ; Lawler, SD; Venitt, S (Jul 15, 1978). "Chromosomal damage and hair dyes". Lancet. 2 (8081): 124–7. doi:10.1016/s0140-6736(78)91508-8. PMID 78325.
  13. ^ Lawler, SD; Fisher, RA; Pickthall, VJ; Povey, S; Evans, MW (April 1982). "Genetic studies on hydatidiform moles. I. The origin of partial moles". Cancer Genetics and Cytogenetics. 5 (4): 309–20. doi:10.1016/0165-4608(82)90096-6. PMID 6284349.
  14. ^ Bagshawe, KD; Lawler, SD (April 1982). "Unmasking moles". British Journal of Obstetrics and Gynaecology. 89 (4): 255–7. doi:10.1111/j.1471-0528.1982.tb04692.x. PMID 6280746.
  15. ^ Fisher, RA; Johnson, PH; Povey, S; Hopkinson, DA; Lawler, SD (November 1993). "ABO genotyping of complete hydatidiform moles". Disease Markers. 11 (4): 179–85. doi:10.1155/1993/750349. PMID 8112022.
  16. ^ "Royal Society of Medicine Sylvia Lawler prize".