Search Results - "Kye Yoon Park"

Contribution of Hepatic Lineage Stage-Specific Donor Memory to the Differential Potential of Induced Mouse Pluripotent Stem Cells by Lee, Seung Bum, Seo, Daekwan, Choi, Dongho, Park, Kye-Yoon, Holczbauer, Agnes, Marquardt, Jens U., Conner, Elizabeth A., Factor, Valentina M., Thorgeirsson, Snorri S.

“…Recent studies suggested that induced pluripotent stem cells (iPSCs) retain a residual donor cell gene expression, which may impact their capacity to…”
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Analysis of the H19ICR Insulator by Yoon, Young Soo, Jeong, Sangkyun, Rong, Qi, Park, Kye-Yoon, Chung, Jae Hoon, Pfeifer, Karl

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Toward xeno-free culture of human embryonic stem cells by Mallon, Barbara S., Park, Kye-Yoon, Chen, Kevin G., Hamilton, Rebecca S., McKay, Ronald D.G.

“…The culture of human embryonic stem cells (hESCs) is limited, both technically and with respect to clinical potential, by the use of mouse embryonic…”
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Large-scale time-lapse microscopy of Oct4 expression in human embryonic stem cell colonies by Bhadriraju, Kiran, Halter, Michael, Amelot, Julien, Bajcsy, Peter, Chalfoun, Joe, Vandecreme, Antoine, Mallon, Barbara S., Park, Kye-yoon, Sista, Subhash, Elliott, John T., Plant, Anne L.

“…Identification and quantification of the characteristics of stem cell preparations is critical for understanding stem cell biology and for the development and…”
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Δ133p53 represses p53-inducible senescence genes and enhances the generation of human induced pluripotent stem cells by Horikawa, Izumi, Park, Kye-yoon, Isogaya, Kazunobu, Hiyoshi, Yukiharu, Li, Han, Anami, Katsuhiro, Robles, Ana I, Mondal, Abdul M, Fujita, Kaori, Serrano, Manuel, Harris, Curtis C

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Hepatic Differentiation from Human Embryonic Stem Cells Using Stromal Cells by Yu, Young-Dong, M.D., Ph.D, Kim, Ki-Hun, M.D., Ph.D, Lee, Sung-Gyu, M.D., Ph.D, Choi, Sang-Yong, M.D., Ph.D, Kim, Young-Chul, M.D., Ph.D, Byun, Kwan-Su, M.D., Ph.D, Cha, In-Ho, M.D., Ph.D, Park, Kye-Yoon, Ph.D, Cho, Cheul-Hyung, Ph.D, Choi, Dong-Ho, M.D., Ph.D

“…Objective The derivation of hepatocytes from human embryonic stem (hES) cells is of value both in the study of early human liver organogenesis and in the…”
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Long-term survival and differentiation of retinal neurons derived from human embryonic stem cell lines in un-immunosuppressed mouse retina by Hambright, Dustin, Park, Kye-Yoon, Brooks, Matthew, McKay, Ron, Swaroop, Anand, Nasonkin, Igor O

“…To examine the potential of NIH-maintained human embryonic stem cell (hESC) lines TE03 and UC06 to differentiate into retinal progenitor cells (hESC-RPCs)…”
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The H19 Differentially Methylated Region Marks the Parental Origin of a Heterologous Locus without Gametic DNA Methylation by Park, Kye-Yoon, Sellars, Elizabeth A., Grinberg, Alexander, Huang, Sing-Ping, Pfeifer, Karl

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A series of west European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin by DAGVADORJ, Ayush, OLIVE, Montse, DALAKAS, Marinos C, GOLDFARB, Lev G, URTIZBEREA, Jean-Andoni, HALLE, Martin, SHATUNOV, Alexey, BÖNNEMANN, Carsten, PARK, Kye-Yoon, GOEBEL, Hans H, FERRER, Isidro, VICART, Patrick

“…Desminopathy is a familial or sporadic cardiac and skeletal muscular dystrophy associated with mutations in desmin. We have previously characterized a de novo…”
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Epigenetic interplay by Pfeifer, Karl, Park, Kye-Yoon

“…In a new study, the presence of a CpG island transgene protects neighboring sequence from DNA methylation during development leading to an open chromatin state…”
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene by Dalakas, Marinos C, Park, Kye-Yoon, Semino-Mora, Cristina, Lee, Hee Suk, Sivakumar, Kumaraswamy, Goldfarb, Lev G

“…Myofibrillar or desmin-related myopathies are a heterogeneous group of severe, dominantly inherited, skeletal myopathies, often accompanied by cardiomyopathy,…”
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Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation by Park, Kye-Yoon, Dalakas, Marinos C, Semino-Mora, Christina, Lee, Hee-Suk, Litvak, Svetlana, Takeda, Kazuyo, Ferrans, Victor J, Goldfarb, Lev G

“…Desmin myopathy is a familial or sporadic disorder characterized by intracytoplasmic accumulation of desmin in the muscle cells. We and others have previously…”
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Missense mutations in desmin associated with familial cardiac and skeletal myopathy by Goldfarb, Lev G, Park, Kye-Yoon, Cervenáková, Larisa, Gorokhova, Svetlana, Lee, Hee-Suk, Vasconcelos, Olavo, Nagle, James W, Semino-Mora, Christina, Sivakumar, Kumaraswamy, Dalakas, Marinos C

“…Desmin-related myopathy (OMIM 601419) is a familial disorder characterized by skeletal muscle weakness associated with cardiac conduction blocks, arrhythmias…”
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Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS) by Cervenakova, Larisa, Protas, Iosif I, Hirano, Asao, Votiakov, Veniamin I, Nedzved, Mikhail K, Kolomiets, Natalia D, Taller, Inna, Park, Kye-Yoon, Sambuughin, Nyamkhishig, Gajdusek, D.Carleton, Brown, Paul, Goldfarb, Lev G

“…Twelve cases of adult-onset progressive muscular atrophy variant of amyotrophic lateral sclerosis (PMA/ALS) were studied in a small rural population of 1500 in…”
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총회구연 : 그랜드볼룸 ; 인간배아줄기세포와 인간역분화만능줄기세포의 간세포 분화능에 대한 비교연구 (초) by Dong Ho Choi, Kye Yoon Park, Jeon Hoon Heo, Cheul Hyung Cho, Marian Durkin, Agnes Holczbauer, Jens U. Marquardt, Valentina M. Factor, Karim Si Tayeb, Stephen A. Duncan, Snorri S. Thorgeirsson

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A transcriptional insulator at the imprinted H19/Igf2 locus by Kaffer, C R, Srivastava, M, Park, K Y, Ives, E, Hsieh, S, Batlle, J, Grinberg, A, Huang, S P, Pfeifer, K

“…Igf2 and H19 exhibit parent-of-origin-specific monoallelic expression. H19 is expressed from the maternal chromosome and Igf2 from the paternal. The two genes…”
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Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations by Dalakas, Marinos C., Dagvadorj, Ayush, Goudeau, Bertrand, Park, Kye-Yoon, Takeda, Kazuyo, Simon-Casteras, Monique, Vasconcelos, Olavo, Sambuughin, Nyamkhishig, Shatunov, Alexey, Nagle, James W., Sivakumar, Kumaraswamy, Vicart, Patrick, Goldfarb, Lev G.

“…Desmin myopathy is a familial or sporadic disorder characterized by the presence of desmin mutations that cause skeletal muscle weakness associated with…”
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Delta 133p53 represses p53-inducible senescence genes and enhances the generation of human induced pluripotent stem cells by Horikawa, Izumi, Park, Kye-yoon, Isogaya, Kazunobu, Hiyoshi, Yukiharu, Li, Han, Anami, Katsuhiro, Robles, Ana I, Mondal, Abdul M, Fujita, Kaori, Serrano, Manuel, Harris, Curtis C

“…p53 functions to induce cellular senescence, which is incompatible with self-renewal of pluripotent stem cells such as induced pluripotent stem cells (iPSC)…”
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Abstract 922: Delta133p53 represses p53-inducible senescence genes and enhances the generation of human induced pluripotent stem cells by Horikawa, Izumi, Park, Kye-yoon, Li, Han, Isogaya, Kazunobu, Hiyoshi, Yukiharu, Anami, Katsuhiro, Robles, Ana I., Mondal, Abdul M., Fujita, Kaori, Serrano, Manuel, Harris, Curtis C.

“…Abstract p53 functions to induce cellular senescence and apoptosis, which can be incompatible with self-renewal of pluripotent stem cells such as induced…”
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[Delta]133p53 represses p53-inducible senescence genes and enhances the generation of human induced pluripotent stem cells by Horikawa, Izumi, Park, Kye-yoon, Isogaya, Kazunobu, Hiyoshi, Yukiharu, Li, Han, Anami, Katsuhiro, Robles, Ana I, Mondal, Abdul M, Fujita, Kaori, Serrano, Manuel, Harris, Curtis C

“…p53 functions to induce cellular senescence, which is incompatible with self-renewal of pluripotent stem cells such as induced pluripotent stem cells (iPSC)…”
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