Shiang, Rita: search on Z-Library

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1

Chromosomal Syndromes

Journal:

Atlas of the Oral and Maxillofacial Surgery Clinics

Year:

2014

Language:

english

File:

PDF, 1.83 MB

english, 2014

2

The CEPH Consortium Linkage Map of Human Chromosome 13

Anne M. Bowcock, Steven C. Gerken, Robert I. Barnes, Rita Shiang, Ethylin Wang Jabs, Andrew C. Warren, Stylianos Antonarakis, Andries E. Retief, Gilles Vergnaud, Mark Leppert, Jean-Marc Lalouel, Raymo

Journal:

Year:

1993

File:

PDF, 638 KB

1993

3

Genomewide analysis of gene expression associated with Tcof1 in mouse neuroblastoma

Michael Mogass, Timothy P. York, Lin Li, Sinitdhorn Rujirabanjerd, Rita Shiang

Journal:

Biochemical and Biophysical Research Communications

Year:

2004

Language:

english

File:

PDF, 630 KB

english, 2004

4

Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

Shiang, Rita, Ryan, Stephen G., Zhu, Ya-Zhen, Hahn, Angelika F., O'Connell, Peter, Wasmuth, John Jacob

Journal:

Nature Genetics

Year:

1993

File:

PDF, 868 KB

1993

5

Mutations in ANKH Cause Chondrocalcinosis

Adrian Pendleton, Michelle D. Johnson, Anne Hughes, Kyle A. Gurley, Andrew M. Ho, Michael Doherty, Josh Dixey, Pierre Gillet, Damien Loeuille, Rodney McGrath, Antonio Reginato, Rita Shiang, Gary Wrigh

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 753 KB

english, 2002

6

GrantSlam 4.0.4

Journal:

Biotech Software & Internet Report

Year:

2001

Language:

english

File:

PDF, 526 KB

english, 2001

7

GrantSlam 5.0.1

Journal:

Biotech Software & Internet Report

Year:

2002

Language:

english

File:

PDF, 598 KB

english, 2002

8

A Homozygous Mutation in a Novel Zinc-Finger Protein, ERIS, Is Responsible for Wolfram Syndrome 2

Sami Amr, Cindy Heisey, Min Zhang, Xia-Juan Xia, Kathryn H. Shows, Kamel Ajlouni, Arti Pandya, Leslie S. Satin, Hatem El-Shanti, Rita Shiang

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 3.63 MB

english, 2007

9

Vector NTI Suite 2.0 v5.5.1

Journal:

Biotech Software & Internet Report

Year:

2000

Language:

english

File:

PDF, 617 KB

english, 2000

10

Mutational analysis of familial and sporadic hyperekplexia

Dr Rita Shiang, Stephen G. Ryan, Ya-Zhen Zhu, Thomas J. Fielder, Richard J. Allen, Alan Fryer, Sumimasa Yamashita, Peter O'Connell, John J. Wasmuth

Journal:

Annals of Neurology

Year:

1995

Language:

english

File:

PDF, 679 KB

english, 1995

11

Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3

Tavormina, Patricia L., Shiang, Rita, Thompson, Leslie M., Zhu, Ya-Zhen, Wilkin, Douglas J., Lachman, Ralph S., Wilcox, William R., Rimoin, David L., Cohn, Daniel H., Wasmuth, John J.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 951 KB

1995

12

A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse

Handford, Cheryl A., Segura, Lillian, Shiang, Rita, Wasmuth, John J., Camper, Sally A., Schofield, Peter, O'Connell, Peter, Ryan, Stephen G., Buckwalter, Marion S., Lynch, Joseph W.

Journal:

Nature Genetics

Year:

1994

File:

PDF, 699 KB

1994

13

Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK

Ernst Reichenberger, Valdenize Tiziani, Shoji Watanabe, Lucy Park, Yasuyoshi Ueki, Carla Santanna, Scott T. Baur, Rita Shiang, Dorothy K. Grange, Peter Beighton, Jessica Gardner, Herman Hamersma, Sean

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 793 KB

english, 2001

14

ReducedTCOF1mRNA level in a rhesus macaque with Treacher Collins-like syndrome: further evidence for haploinsufficiency of treacle as the cause of disease

Kathryn H. Shows, Christy Ward, Laura Summers, Lin Li, Gregory R. Ziegler, Andrew G. Hendrickx, Rita Shiang

Journal:

Mammalian Genome

Year:

2006

Language:

english

File:

PDF, 764 KB

english, 2006

15

Why Do Faculty Leave? Reasons for Attrition of Women and Minority Faculty from a Medical School: Four-Year Results

Cropsey, Karen L., Masho, Saba W., Shiang, Rita, Sikka, Veronica, Kornstein, Susan G., Hampton, Carol L.

Journal:

Journal of Women's Health

Year:

2008

Language:

english

File:

PDF, 192 KB

english, 2008

16

Regulation of the Mouse Treacher Collins Syndrome Homolog ( Tcof1 ) Promoter Through Differential Repression of Constitutive Expression

Shows, Kathryn H., Shiang, Rita

Journal:

DNA and Cell Biology

Year:

2008

Language:

english

File:

PDF, 441 KB

english, 2008

17

Mapping of the human complement factor I gene to 4q25

Shiang, Rita, Murray, Jeffrey C., Morton, Cynthia C., Buetow, Kenneth H., Wasmuth, John J., Olney, Ann Haskins, Sanger, Warren G., Goldberger, Gabriel

Journal:

Year:

1989

Language:

english

File:

PDF, 853 KB

english, 1989

18

Conventional versus pigtail chest tube—are they similar for treatment of malignant pleural effusions?

Mendes, Maria Aurora, China Pereira, Nuno, Ribeiro, Carla, Vanzeller, Manuela, Shiang, Teresa, Gaio, Rita, Campainha, Sérgio

Journal:

Supportive Care in Cancer

Year:

2018

Language:

english

File:

PDF, 366 KB

english, 2018

19

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease

Rees, Mark I, Harvey, Kirsten, Pearce, Brian R, Chung, Seo-Kyung, Duguid, Ian C, Thomas, Philip, Beatty, Sarah, Graham, Gail E, Armstrong, Linlea, Shiang, Rita

Journal:

Nature Genetics

Year:

2006

Language:

english

File:

PDF, 940 KB

english, 2006

20

Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci

Jeffrey C. Murray, Rita Shiang, Leon R. Carlock, Moyra Smith, Kenneth H. Buetow

Journal:

Year:

1987

Language:

english

File:

PDF, 612 KB

english, 1987

21

Reference Manager 10

Journal:

Biotech Software & Internet Report

Year:

2002

Language:

english

File:

PDF, 1.04 MB

english, 2002

22

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Rita Shiang, Leslie M. Thompson, Ya-Zhen Zhu, Deanna M. Church, Thomas J. Fielder, Maureen Bocian, Sara T. Winokur, John J. Wasmuth

Journal:

Year:

1994

Language:

english

File:

PDF, 1.27 MB

english, 1994

23

Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3 : Beyond crouzon syndrome and acanthosis nigricans

Rymer, Karen, Shiang, Rita, Hsiung, Anting, Pandya, Arti, Bigdeli, Tim, Webb, Bradley T., Rhodes, Jennifer

Journal:

Molecular Genetics & Genomic Medicine

Year:

2019

Language:

english

File:

PDF, 486 KB

english, 2019

24

Studies of the Candidate Genes TGFB2, MSX1, TGFA, and TGFB3 in the Etiology of Cleft Lip and Palate in the Philippines

Lidral, Andrew C., Murray, Jeffrey C., Buetow, Kenneth H., Basart, Ann M., Schearer, Heidi, Shiang, Rita, Naval, Avelina, Layda, Eriberto, Magee, Kathy, Magee, William

Journal:

The Cleft Palate-Craniofacial Journal

Year:

1997

File:

PDF, 353 KB

1997

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