Mills PL - Search Results

1

Effect of family history on disclosure patterns of cystic fibrosis carrier status.

Ormond KE, Mills PL, Lester LA, Ross LF. Ormond KE, et al. Among authors: mills pl. Am J Med Genet C Semin Med Genet. 2003 May 15;119C(1):70-7. doi: 10.1002/ajmg.c.10008. Am J Med Genet C Semin Med Genet. 2003. PMID: 12704640

2

Urorectal septal defects in a female and her offspring.

Mills PL, Pergament E. Mills PL, et al. Am J Med Genet. 1997 Jun 13;70(3):250-2. doi: 10.1002/(sici)1096-8628(19970613)70:3<250::aid-ajmg7>3.0.co;2-#. Am J Med Genet. 1997. PMID: 9188661

3

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

Matsumoto N, Leventer RJ, Kuc JA, Mewborn SK, Dudlicek LL, Ramocki MB, Pilz DT, Mills PL, Das S, Ross ME, Ledbetter DH, Dobyns WB. Matsumoto N, et al. Among authors: mills pl. Eur J Hum Genet. 2001 Jan;9(1):5-12. doi: 10.1038/sj.ejhg.5200548. Eur J Hum Genet. 2001. PMID: 11175293

4

The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene.

Cardoso C, Leventer RJ, Matsumoto N, Kuc JA, Ramocki MB, Mewborn SK, Dudlicek LL, May LF, Mills PL, Das S, Pilz DT, Dobyns WB, Ledbetter DH. Cardoso C, et al. Among authors: mills pl. Hum Mol Genet. 2000 Dec 12;9(20):3019-28. doi: 10.1093/hmg/9.20.3019. Hum Mol Genet. 2000. PMID: 11115846

5

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME. Pilz DT, et al. Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029. Hum Mol Genet. 1998. PMID: 9817918

6

X-linked malformations of cortical development.

Leventer RJ, Mills PL, Dobyns WB. Leventer RJ, et al. Among authors: mills pl. Am J Med Genet. 2000 Fall;97(3):213-20. doi: 10.1002/1096-8628(200023)97:3<213::AID-AJMG1039>3.0.CO;2-W. Am J Med Genet. 2000. PMID: 11449490 Review.

7

Characterization of mutations in fifty North American patients with X-linked myotubular myopathy.

Herman GE, Kopacz K, Zhao W, Mills PL, Metzenberg A, Das S. Herman GE, et al. Among authors: mills pl. Hum Mutat. 2002 Feb;19(2):114-21. doi: 10.1002/humu.10033. Hum Mutat. 2002. PMID: 11793470

8

Kinetics and thermodynamics of thermal inactivation for recombinant Escherichia coli cellulases, cel12B, cel8C, and polygalacturonase, peh28; biocatalysts for biofuel precursor production.

Ibrahim E, Mahmoud A, Jones KD, Taylor KE, Hosseney EN, Mills PL, Escudero JM. Ibrahim E, et al. Among authors: mills pl. J Biochem. 2021 Feb 6;169(1):109-117. doi: 10.1093/jb/mvaa097. J Biochem. 2021. PMID: 32810224

9

Molecular and biochemical characterization of recombinant cel12B, cel8C, and peh28 overexpressed in Escherichia coli and their potential in biofuel production.

Ibrahim E, Jones KD, Taylor KE, Hosseney EN, Mills PL, Escudero JM. Ibrahim E, et al. Among authors: mills pl. Biotechnol Biofuels. 2017 Feb 27;10:52. doi: 10.1186/s13068-017-0732-1. eCollection 2017. Biotechnol Biofuels. 2017. PMID: 28413443 Free PMC article.

10

A citrus waste-based biorefinery as a source of renewable energy: technical advances and analysis of engineering challenges.

Rivas-Cantu RC, Jones KD, Mills PL. Rivas-Cantu RC, et al. Among authors: mills pl. Waste Manag Res. 2013 Apr;31(4):413-20. doi: 10.1177/0734242X13479432. Epub 2013 Feb 25. Waste Manag Res. 2013. PMID: 23439875

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