McKeown CM - Search Results

1

Adenine nucleotide tissue concentrations and liver allograft viability after cold preservation and warm ischemia.

Harvey PR, Iu S, McKeown CM, Petrunka CN, Ilson RG, Strasberg SM. Harvey PR, et al. Among authors: mckeown cm. Transplantation. 1988 Jun;45(6):1016-20. doi: 10.1097/00007890-198806000-00004. Transplantation. 1988. PMID: 3289145

2

Sinusoidal lining cell damage: the critical injury in cold preservation of liver allografts in the rat.

McKeown CM, Edwards V, Phillips MJ, Harvey PR, Petrunka CN, Strasberg SM. McKeown CM, et al. Transplantation. 1988 Aug;46(2):178-91. Transplantation. 1988. PMID: 3043774

3

The challenges of obesity for fertility: A FIGO literature review.

Gautam D, Purandare N, Maxwell CV, Rosser ML, O'Brien P, Mocanu E, McKeown C, Malhotra J, McAuliffe FM; FIGO Committee on Impact of Pregnancy on Long-term Health and the FIGO Committee on Reproductive Medicine, Endocrinology and Infertility. Gautam D, et al. Int J Gynaecol Obstet. 2023 Jan;160 Suppl 1(Suppl 1):50-55. doi: 10.1002/ijgo.14538. Int J Gynaecol Obstet. 2023. PMID: 36635080 Free PMC article. Review.

4

PMS2 mutations in childhood cancer.

De Vos M, Hayward BE, Charlton R, Taylor GR, Glaser AW, Picton S, Cole TR, Maher ER, McKeown CM, Mann JR, Yates JR, Baralle D, Rankin J, Bonthron DT, Sheridan E. De Vos M, et al. Among authors: mckeown cm. J Natl Cancer Inst. 2006 Mar 1;98(5):358-61. doi: 10.1093/jnci/djj073. J Natl Cancer Inst. 2006. PMID: 16507833

5

An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function.

Caronia G, Goodman FR, McKeown CM, Scambler PJ, Zappavigna V. Caronia G, et al. Among authors: mckeown cm. Development. 2003 Apr;130(8):1701-12. doi: 10.1242/dev.00396. Development. 2003. PMID: 12620993

6

Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition.

Wallis YL, Morton DG, McKeown CM, Macdonald F. Wallis YL, et al. Among authors: mckeown cm. J Med Genet. 1999 Jan;36(1):14-20. J Med Genet. 1999. PMID: 9950360 Free PMC article.

7

Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndrome.

Renwick PJ, Birley AJ, McKeown CM, Hultén M. Renwick PJ, et al. Among authors: mckeown cm. Clin Genet. 1995 Aug;48(2):80-4. doi: 10.1111/j.1399-0004.1995.tb04060.x. Clin Genet. 1995. PMID: 7586656

8

Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis.

Wallis YL, Macdonald F, Hultén M, Morton JE, McKeown CM, Neoptolemos JP, Keighley M, Morton DG. Wallis YL, et al. Among authors: mckeown cm. Hum Genet. 1994 Nov;94(5):543-8. doi: 10.1007/BF00211023. Hum Genet. 1994. PMID: 7959691

9

Exclusion of an elastin gene (ELN) mutation as the cause of pseudoxanthoma elasticum (PXE) in one family.

Raybould MC, Birley AJ, Moss C, Hultén M, McKeown CM. Raybould MC, et al. Among authors: mckeown cm. Clin Genet. 1994 Jan;45(1):48-51. doi: 10.1111/j.1399-0004.1994.tb03990.x. Clin Genet. 1994. PMID: 8149653

10

Rapid interphase FISH diagnosis of trisomy 18 on blood smears.

McKeown CM, Waters JJ, Stacey M, Newman BF, Cardy DL, Hultén M. McKeown CM, et al. Lancet. 1992 Aug 22;340(8817):495. doi: 10.1016/0140-6736(92)91823-q. Lancet. 1992. PMID: 1354828 No abstract available.

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