|
|
|
|
A-Z Articles Index by First Author's Last Name |
| Padiath QS et al. Lamin B1 duplications cause autosomal dominant leukodystrophy. Nat Genet. 2006 Sep 3; [Epub ahead of print] |
| Paez JG et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science. 2004 Jun 4; 304(5676): 1497-500. Epub 2004 Apr 29. |
| Panov AV et al. Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines. Nat Neurosci. 2002;5:731-6. |
| Pao W et al. EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib.Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13306-11. Epub 2004 Aug 25. |
| Parrini A et al. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. Brain. 2006 Jul;129(Pt 7):1892-906. Epub 2006 May 9. |
| Parry DA et al. Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. Am J Hum Genet. 2009 Feb;84(2):266-73. Epub 2009 Feb 5. |
| Pask A et al. The human sex-reversing ATRX gene has a homologue on the marsupial Y chromosome, ATRY: Implications for the evolution of mammalian sex determination. PNAS 97(24), 2000. |
| Patil, N., et al. (2001) Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 294:1719-1723. |
| Pendas AM et al. Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice. Nat Genet. 2002 May;31(1):94-9. Epub 2002 Apr 01. |
Peng Y et al. A critical role of Pax6 in alcohol-induced fetal microcephaly. Neurobiol Dis. 2004 Jul;16(2):370-6. |
| Perry GH et al. Diet and the evolution of human amylase gene copy number variation. 2007 Nature Genetics; 39:1256-1260 |
| Peterson P et al. APECED: a monogenic autoimmune disease providing new clues to self-tolerance. Immunol Today 1998;19(9):384-6. |
| Pfeifer, A et al. Delivery of the Cre recombinaase by a self-deleting lentiviral vector: Efficient gene targeting in vivo. PNAS 98, 11450 -11455 (2001). |
| Pokholok DK et al. Genome-wide Map of Nucleosome Acetylation and Methylation in Yeast. Cell. 2005 Aug 26;122(4):517-27. |
| Polok B et al. Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta. Am J Hum Genet. 2009 Feb;84(2):259-65. Epub 2009 Feb 5. |
| Pontes O et al. The Arabidopsis chromatin-modifying nuclear siRNA pathway involves a nucleolar RNA processing center. Cell. 2006 Jul 14;126(1):79-92. |
| Price AL et al. Discerning the ancestry of European Americans in genetic association studies. PLoS Genet. 2008 Jan;4(1):e236. Epub 2007 Nov 19. |
| Pujana, M.A., et al. (2001) Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26. Genome Res 11(1):98-111. |
| Pujana, M.A., et al. (2002) Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons. Eur J Hum Genet 10(1):26-35. |
| Purandare SM et al. A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice. Development. 2002 May;129(9): 2293-302. |