lyonlab.labsites.cshl.edu

Lyon Lab |

Most recently, we have just published the discovery of an entirely new intellectual disability and neurologic syndrome involving mutations in the gene TAF1, involved in the initiation of transcription. This discovery also has implications for the pathogenesis of a more common disease in the Phillipines, called X-linked dystonia parkinsonism. Link to work by Gholson Lyon in CSHL Repository. And in Google Scholar. Gholson Lyon On Twitter. Gholson Lyon on Linkedin. Gholson Lyon on Youtube.

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Lyon Lab | | lyonlab.labsites.cshl.edu Reviews

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Most recently, we have just published the discovery of an entirely new intellectual disability and neurologic syndrome involving mutations in the gene TAF1, involved in the initiation of transcription. This discovery also has implications for the pathogenesis of a more common disease in the Phillipines, called X-linked dystonia parkinsonism. Link to work by Gholson Lyon in CSHL Repository. And in Google Scholar. Gholson Lyon On Twitter. Gholson Lyon on Linkedin. Gholson Lyon on Youtube.

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2 lab photos

3 publications

4 presentations

5 journal clubs

6 teaching lectures

7 media coverage

8 introduction

9 and in pubmed

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Lyon Lab | | lyonlab.labsites.cshl.edu Reviews

https://lyonlab.labsites.cshl.edu

Most recently, we have just published the discovery of an entirely new intellectual disability and neurologic syndrome involving mutations in the gene TAF1, involved in the initiation of transcription. This discovery also has implications for the pathogenesis of a more common disease in the Phillipines, called X-linked dystonia parkinsonism. Link to work by Gholson Lyon in CSHL Repository. And in Google Scholar. Gholson Lyon On Twitter. Gholson Lyon on Linkedin. Gholson Lyon on Youtube.

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lyonlab.labsites.cshl.edu

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Lyon Lab | People

http://lyonlab.labsites.cshl.edu/people

PhD student ( View Han Fang’s Github page. Han Fang received his M.S. in Applied Math & Statistics at Stony Brook University and B.S. in Optical Informatics at Sun Yat-sen University, China. He is currently a Ph.D. student supervised by Dr. Michael Schatz. And Dr. Gholson Lyon. At Cold Spring Harbor Laboratory. Since joining the Lyon Lab in 2013, Han has been focusing on the analysis of exome and whole genome data, especially for the detection of INDELs ( paper here. June 2014 - August 2016. Partners for...

2

Lyon Lab | Presentations

http://lyonlab.labsites.cshl.edu/presentations

Previous Invited Talks &. December 2016) Amino-terminal acetylation of proteins - why? Seminar, Cold Spring Harbor Laboratory In-House Seminar Series, Cold Spring Harbor, NY. November 2016) Human Genetics and Rare Diseases. Seminar, Cold Spring Harbor Laboratory In-House Seminar Series, Cold Spring Harbor, NY In-House Thanksgiving Symposium LYON Nov 2016. July 2016) The X-Linked Ogden Syndrome Involving NAA10 and the Amino-Terminal Acetylation of Proteins in Human Biology and Disease. January 2016) A rar...

3

Lyon Lab | Journal Clubs

http://lyonlab.labsites.cshl.edu/journal-clubs

Hyper)tension release by N-terminal acetylation / Control of mammalian G protein signaling by N-terminal acetylation and the N-end rule pathway. View journal club slides). Sporulation in the Budding Yeast. View journal club slides). Association of Protein Biogenesis Factors at the Yeast Ribosomal Tunnel Exit is Affected by the Translational Status and Nascent Polypeptide Sequence. View journal club slides). The principle of antagonism ensures protein targeting specificity at the endoplasmic reticulum.

4

Lyon Lab | Teaching Lectures

http://lyonlab.labsites.cshl.edu/teaching-mentoring-and-public-education-experience

Previous Teaching, Mentoring and Public Education Experience. Lecture to Stony Brook University Chemical Biology Graduate Students on “N-Terminal acetyltransferases and Translation”. Lecture to Stony Brook Genetics Graduate Students on “Human Genetic Variation and the Genotype-Phenotype Problem”. Lecture to Stony Brook University GE510: Graduate Genetics Students Human Genetics and the Genotype-Phenotype Problem. View Online Video 1). View Online Video 2). Lecture to Watson School Graduate Students on Hu...

5

Lyon Lab | Publications

http://lyonlab.labsites.cshl.edu/publications

Yang H, Chen G, Lima L, Fang H, Jimenez-Barron LT, Li M, Lyon GJ. 2015) PennCNV-Hadoop: Accurate Detection of Copy Number Variation from Whole Genome Sequencing Data. Publications (as a Principal Investigator). Fang H, Wu Y, Jiménez-Barrón LT, O’Rawe JA, Highnam G, Mittelman G, Lyon GJ. 2016) Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine. BMC Med Genomics. 2017 Feb 23;10(1):10. doi: 10.1186/s12920-017-0246-5. PMID: 28228131. (View PDF). Nucleic Acids Res&#46...

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Most recently, we have just published the discovery of an entirely new intellectual disability and neurologic syndrome involving mutations in the gene TAF1, involved in the initiation of transcription. This discovery also has implications for the pathogenesis of a more common disease in the Phillipines, called X-linked dystonia parkinsonism. Link to work by Gholson Lyon in CSHL Repository. And in Google Scholar. Gholson Lyon On Twitter. Gholson Lyon on Linkedin. Gholson Lyon on Youtube.

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