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A-Z Articles Index by First Author's Last Name |
| Lagouge M et al. Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1alpha. Cell 2006 Dec 15; 127:1-14. link to article PDF at cell.com homepage. |
| Lai CS et al. A forkhead-domain gene is mutated in severe speech and language disorder. Nature. 2001; 413 (6855):519-23. |
| Lam KW & Jeffreys AJ. Processes of de novo duplication of human alpha-globin genes. PNAS 2007 104 (26): 10950-5. Epub 2007 Jun 15. |
| Lamason RL et al. SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science. 2005 Dec 16;310(5755):1782-6. |
| Lamb J et al. A mechanism of cyclin D1 action encoded in the patterns of gene expression in human cancer. Cell. 2003 Aug 8;114(3):323-34. |
| Larsson M et al. Importance of genetic effects for characteristics of the human iris. Twin Res. 2003 Jun;6(3):192-200. |
| Laurikkala J et al. Regulation of hair follicle development by the TNF signal ectodysplasin and its receptor Edar. Development. 2002;129:2541-53. |
| Lee JS et al. Application of comparative functional genomics to identify best-fit mouse models to study human cancer. Nat Genet. 2004 Dec;36(12):1306-11. Epub 2004 Nov |
| Lee, JT Regulation of X-chromosome counting by Tsix and Xite sequences. Science. 2005 Jul 29;309(5735):768-71. |
| Lee SJ. Quadrupling muscle mass in mice by targeting TGF-beta signaling pathways.PLoS ONE. 2007 Aug 29;2(8):e789. |
| Leehey MA et al. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers. Neurology. 2007 Dec 5; [Epub ahead of print] |
| Leibiger IB & Berggren PO. Sirt1: a metabolic master switch that modulates lifespan. Nat Med. 2006 Jan;12(1):34-6; discussion 36. |
| Lerner-Ellis JP et al. Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type. Nat Genet. 2006 Jan;38(1):93-100. Epub 2005 Nov 27. |
| Lesnik Oberstein SA et al. Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase. Am J Hum Genet. 2006 Sep;79(3):562-6. |
| Ley TJ et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature. 2008 Nov 6;456(7218):66-72 |
| Li B & Leal SM. Discovery of rare variants via sequencing: implications for the design of complex trait association studies. PLoS Genet. 2009 May;5(5):e1000481. Epub 2009 May 15. |
| Li CF et al. An ARGONAUTE4-containing nuclear processing center colocalized with Cajal bodies in Arabidopsis thaliana. Cell. 2006 Jul 14;126(1):93-106. |
| Li JZ et al. Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation. Science. 2008 Feb 22;319(5866):1100-4. |
| Liao SM. Rescuing human embryonic stem cell research: the Blastocyst Transfer Method. Am J Bioeth. 2005 Nov-Dec;5(6):8-16. |
| Lieberman RL et al. Structure of acid beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease. Nat Chem Biol. 2007 Feb;3(2):101-7. |
| Lim U et al. Consumption of aspartame-containing beverages and incidence of hematopoietic and brain malignancies. Cancer Epidemiol Biomarkers Prev. 2006 Sep;15(9):1654-9. |
Limongelli A et al. Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genome. J Med Genet. 2004 May; 41 (5): 342-9. |
| Lin TK et al. Specific modification of mitochondrial protein thiols in response to oxidative stress. J Biol Chem. 2002;277:17048-17056. |
| Linardopoulou EV et al. Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication. Nature 437:94-100. Sep 1, 2005 |
Linglart A et al., A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS. Am J Hum Genet. 2005 May;76(5):804-14. Epub 2005 Mar 30. |
| Lipton L et al. Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway. Cancer Res. 2003 Nov 15;63(22):7595-9. |
| Liu F et al. A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population. Am J Hum Genet. 2007 Jul;81(1):17-31. Epub 2007 May 29. |
Liu J et al., Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit. Proc Natl Acad Sci U S A. 2005 Apr 12;102(15):5513-8. Epub 2005 Apr 5. |
| Liu KJ at al. Chemical rescue of cleft palate and midline defects in conditional GSK-3B mice. Nature. 2007 Mar 1;446(7131):79-82. Epub 2007 Feb 11. |
| Locke DP et al. Molecular evolution of the human chromosome 15 pericentromeric region. Cytogenet Genome Res. 2005;108(1-3):73-82. |
| Loeys et al. Aneurysm syndromes associated with mutations in the TGF-beta receptor genes. N Engl J Med. 2006 Aug 24;355(8):788-98. |
| Loonstra, A et al. Growth inhibition and DNA damage induced by Cre recombinase in mammalian cells. PNAS 98, 9202-9214 (2001) . |
| Lorenz-Depiereux B et al. Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3. Am J Hum Genet. 2006 Feb;78(2):193-201. Epub 2005 Dec 9. |
| Lu J et al. MicroRNA expression profiles classify human cancers. Nature. 2005 Jun 9;435(7043):834-8. |
| Lu XY et al. Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis. Pediatrics. 2008 Dec;122(6):1310-8. |
| Lupski JR. Abstract. Genomic rearrangements and sporadic disease. Nat Genet. 2007; 39 (7 Suppl): S43-7. Review. |
| Lynch TJ et al. Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib.N Engl J Med. 2004 May 20; 350 (21): 2129-39. Epub 2004 Apr 29. |