Kye-yoon Park

发表

Characterization of human embryonic stem cell lines by the International Stem Cell Initiative

G. Churchill, J. Rossant, R. McKay, 2007, Nature Biotechnology.

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

J. Nagle, M. Dalakas, S. Gorokhova, 1998, Nature Genetics.

Toward xeno-free culture of human embryonic stem cells.

R. McKay, B. Mallon, Kevin G. Chen, 2006, The international journal of biochemistry & cell biology.

Contribution of Hepatic Lineage Stage‐Specific Donor Memory to the Differential Potential of Induced Mouse Pluripotent Stem Cells

S. Thorgeirsson, V. Factor, Daekwan Seo, 2012, Stem cells.

Epigenetic interplay

K. Pfeifer, Kye-yoon Park, 2003, Nature Genetics.

Desmin splice variants causing cardiac and skeletal myopathy

V. Ferrans, M. Dalakas, H. Goebel, 2000, Journal of medical genetics.

Analysis of the H19ICR Insulator (cid:1)

J. Chung, K. Pfeifer, Kye-yoon Park, 2007 .

Long-term survival and differentiation of retinal neurons derived from human embryonic stem cell lines in un-immunosuppressed mouse retina

R. McKay, A. Swaroop, I. Nasonkin, 2012, Molecular vision.

Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations

J. Nagle, M. Dalakas, Kye-yoon Park, 2003, Neuromuscular Disorders.

The H19 Differentially Methylated Region Marks the Parental Origin of a Heterologous Locus without Gametic DNA Methylation

A. Grinberg, K. Pfeifer, Kye-yoon Park, 2004, Molecular and Cellular Biology.

Δ133p53 represses p53-inducible senescence genes and enhances the generation of human induced pluripotent stem cells

C. Harris, M. Serrano, A. Robles, 2017, Cell Death and Differentiation.

Large-scale time-lapse microscopy of Oct4 expression in human embryonic stem cell colonies

Peter Bajcsy, Anne L. Plant, Julien Amelot, 2016, Stem cell research.

A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin

I. Ferrer, M. Dalakas, H. Goebel, 2004, Journal of Neurology.

Analysis of the H19ICR Insulator

J. Chung, K. Pfeifer, Kye-yoon Park, 2007, Molecular and Cellular Biology.

Analysis of the H 19 ICR Insulator

J. Chung, K. Pfeifer, Kye-yoon Park, 2007 .

Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation

V. Ferrans, M. Dalakas, Kye-yoon Park, 2000, Clinical genetics.

Hepatic differentiation from human embryonic stem cells using stromal cells.

Sung‐Gyu Lee, Kye-yoon Park, C. Cho, 2011, The Journal of surgical research.

Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS)

Paul Brown, P. Brown, D. Gajdusek, 2000, Journal of the Neurological Sciences.

Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.

M. Dalakas, Kye-yoon Park, K. Sivakumar, 2000, The New England journal of medicine.

Identification of fifteen novel mutations and genotype–phenotype relationship in Fabry disease

R. Schiffmann, J. Nagle, L. Goldfarb, 2001, Clinical genetics.

Abstract 922: Delta133p53 represses p53-inducible senescence genes and enhances the generation of human induced pluripotent stem cells

C. Harris, M. Serrano, A. Robles, 2017 .