Ken-Shiung Chen: search on Z-Library

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1

Advanced Topics in Neurological Disorders || Real-Time Analysis of Intracranial Pressure Waveform Morphology

Chen, Ken-Shiung

Year:

2012

Language:

english

File:

PDF, 1.04 MB

english, 2012

2

10.1038/71743

Lupski, James R., Potocki, Lorraine, Chen, Ken-Shiung, Park, Sung-Sup, Osterholm, Doreen E., Withers, Marjorie A., Kimonis, Virginia, Summers, Anne M., Meschino, Wendy S., Anyane-Yeboa, Kwame, Kashork

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 284 KB

english, 2000

3

Genetic Studies of Prader–Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q

Aihua Hou, Shuan-Pei Lin, Shi Yun Ho, Chi-Fung Jennifer Chen, Hsiang-Yu Lin, Yen-Juin Chen, Chi-Yu Huang, Huei-Ching Chiu, Chih-Kuang Chuang, Ken-Shiung Chen

Journal:

Annals of Human Genetics

Year:

2011

Language:

english

File:

PDF, 663 KB

english, 2011

4

Subunit 3 of the COP9 Signal Transduction Complex Is Conserved from Plants to Humans and Maps within the Smith–Magenis Syndrome Critical Region in 17p11.2

Lorraine Potocki, Ken-Shiung Chen, James R. Lupski

Journal:

Year:

1999

Language:

english

File:

PDF, 90 KB

english, 1999

5

Cloning, Genomic Structure, and Expression of Mouse Ring Finger Protein GeneZnf179

Qi Zhao, Ken-Shiung Chen, Bassem A. Bejjani, James R. Lupski

Journal:

Year:

1998

Language:

english

File:

PDF, 312 KB

english, 1998

6

Genomic Structure, Evolution, and Expression of HumanFLII,a Gelsolin and Leucine-Rich-Repeat Family Member: Overlap withLLGL

Hugh D. Campbell, Shelley Fountain, Ian G. Young, Charles Claudianos, Jörg D. Hoheisel, Ken-Shiung Chen, James R. Lupski

Journal:

Year:

1997

Language:

english

File:

PDF, 801 KB

english, 1997

7

Mouse imprinting defect mutations that model Angelman syndrome

Mei-Yi Wu, Ken-Shiung Chen, Jan Bressler, Aihua Hou, Ting-Fen Tsai, Arthur L. Beaudet

Journal:

Year:

2006

Language:

english

File:

PDF, 598 KB

english, 2006

8

A Physical Map of the Mouseshaker-2Region Contains Many of the Genes Commonly Deleted in Smith–Magenis Syndrome (del17p11.2p11.2)

Frank J. Probst, Ken-Shiung Chen, Qi Zhao, Aihui Wang, Thomas B. Friedman, James R. Lupski, Sally A. Camper

Journal:

Year:

1999

Language:

english

File:

PDF, 155 KB

english, 1999

9

Localization of the Human Nuclear Receptor Corepressor (hN-CoR) Gene between the CMT1A and the SMS Critical Regions of Chromosome 17p11.2

Takashi Nagaya, Ken-Shiung Chen, Miyuki Fujieda, Sachiko Ohmori, Jennifer K. Richer, Kathryn B. Horwitz, James R. Lupski, Hisao Seo

Journal:

Year:

1999

Language:

english

File:

PDF, 139 KB

english, 1999

10

Advanced Topics in Neurological Disorders || Image Analysis for Automatically-Driven Bionic Eye

Chen, Ken-Shiung

Year:

2012

Language:

english

File:

PDF, 1.30 MB

english, 2012

11

Genetic Mapping Refines DFNB3 to 17p11.2, Suggests Multiple Alleles of DFNB3, and Supports Homology to the Mouse Model shaker-2

Yong Liang, Aihui Wang, Frank J. Probst, I. Nyoman Arhya, Thomas D. Barber, Ken-Shiung Chen, Dilip Deshmukh, David F. Dolan, John T. Hinnant, Lynn E. Carter, Pawan K. Jain, Anil K. Lalwani, Xiaoyan C.

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 989 KB

english, 1998

12

Smith-Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization

Ramesh C. Juyal, Frank Greenberg, Gregory A. Mengden, James R. Lupski, Barbara J. Trask, Ger van den Engh, Elizabeth A. Lindsay, Heather Christy, Ken-Shiung Chen, Antonio Baldini, Lisa G. Shaffer, Pra

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 725 KB

english, 1995

13

Novel mutations ofMYO15Aassociated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

Nikki Liburd, Manju Ghosh, Saima Riazuddin, Sadaf Naz, Shaheen Khan, Zubair Ahmed, Sheikh Riazuddin, Yong Liang, Puthezhath S. Menon, Tenesha Smith, Ann C. Smith, Ken-Shiung Chen, James R. Lupski, Edw

Journal:

Year:

2001

Language:

english

File:

PDF, 172 KB

english, 2001

14

The Smith-Magenis syndrome [del(17)p11.2]: Clinical review and molecular advances

Ken-Shiung Chen, Lorraine Potocki, James R. Lupski

Journal:

Development Diabilities Research Reviews

Year:

1996

Language:

english

File:

PDF, 1.05 MB

english, 1996

15

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

Chen, Ken-Shiung, Manian, Prasad, Koeuth, Thearith, Potocki, Lorraine, Zhao, Qi, Chinault, A. Craig, Lee, Cheng Chi, Lupski, James R.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.29 MB

1997

16

DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome

Lorraine Potocki, Ken-Shiung Chen, Thearith Koeuth, James Killian, Susan T. Iannaccone, Stuart K. Shapira, Catherine D. Kashork, Aimee S. Spikes, Lisa G. Shaffer, James R. Lupski

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 281 KB

english, 1999

17

Rasd1 interacts with Ear2 (Nr2f6) to regulate renin transcription

Jen Jen Tan, Shufen Angeline Ong, Ken-Shiung Chen

Journal:

BMC Molecular Biology

Year:

2011

Language:

english

File:

PDF, 1.68 MB

english, 2011

18

UBE3A regulates MC1R expression: a link to hypopigmentation in Angelman syndrome

Daren Low, Ken-Shiung Chen

Journal:

Pigment Cell & Melanoma Research

Year:

2011

Language:

english

File:

PDF, 7.39 MB

english, 2011

19

Advanced Topics in Neurological Disorders || Angelman Syndrome: Proteomics Analysis of an UBE3A Knockout Mouse and Its Implications

Chen, Ken-Shiung

Year:

2012

File:

PDF, 730 KB

2012

20

Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation

Low, Daren, Chen, Ken-Shiung

Journal:

European Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 584 KB

english, 2010

21

Prenatal Diagnosis of Charcot-Marie-Tooth Disease Type 1A

CATHERINE D. KASHORK, KEN-SHIUNG CHEN, JAMES R. LUPSKI, LISA G. SHAFFER

Journal:

Annals of the New York Academy of Sciences

Year:

1999

File:

PDF, 1.05 MB

1999

22

Rasd1 Modulates the Coactivator Function of NonO in the Cyclic AMP Pathway

Ong, Shufen Angeline, Tan, Jen Jen, Tew, Wai Loon, Chen, Ken-Shiung, Partridge, Janet F.

Journal:

Year:

2011

Language:

english

File:

PDF, 1.43 MB

english, 2011

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