Erin E Baschal: search on Z-Library

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1

Sequencing of the TBX6 Gene in Families With Familial Idiopathic Scoliosis

Baschal, Erin E., Swindle, Kandice, Justice, Cristina M., Baschal, Robin M., Perera, Anoja, Wethey, Cambria I., Poole, Alex, Pourquié, Olivier, Tassy, Olivier, Miller, Nancy H.

Journal:

Spine Deformity

Year:

2015

Language:

english

File:

PDF, 1.39 MB

english, 2015

2

The fission yeast DNA structure checkpoint protein Rad26ATRIP/LCD1/UVSDaccumulates in the cytoplasm following microtubule destabilization

Erin E Baschal, Kuan J Chen, Lee G Elliott, Matthew J Herring, Shawn C Verde, Tom D Wolkow

Journal:

BMC Cell Biology

Year:

2006

Language:

english

File:

PDF, 3.55 MB

english, 2006

3

Replication and further characterization of a Type 1 diabetes-associated locus at the telomeric end of the major histocompatibility complex

Erin E. BASCHAL, Suparna A. SARKAR, Theresa A. BOYLE, Janet C. SIEBERT, Jean M. JASINSKI, Katharine R. GRABEK, Taylor K. ARMSTRONG, Sunanda R. BABU, Pamela R. FAIN, Andrea K. STECK, Marian J. REWERS,

Journal:

Journal of Diabetes

Year:

2011

Language:

english

File:

PDF, 1.14 MB

english, 2011

4

High Density SNP Analysis of the MHC Region Reveals Multiple Loci for Type 1A Diabetes

Theresa A. Aly, Erin E. Baschal, Mohamed M. Jahromi, Adam Kretowski, Sunanda R. Babu, Marian J. Rewers, George S. Eisenbarth

Journal:

Clinical Immunology

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

5

Congruence as a measurement of extended haplotype structure across the genome

Erin E Baschal, Jean M Jasinski, Theresa A Boyle, Pamela R Fain, George S Eisenbarth, Janet C Siebert

Journal:

Journal of Translational Medicine

Year:

2012

Language:

english

File:

PDF, 1.26 MB

english, 2012

6

Multi-omic studies on missense PLG variants in families with otitis media

Bootpetch, Tori C., HafrÃ©n, Lena, Elling, Christina L., Baschal, Erin E., Manichaikul, Ani W., Pine, Harold S., Szeremeta, Wasyl, Scholes, Melissa A., Cass, Stephen P., Larson, Eric D., Chan, Kenny H

Journal:

Scientific Reports

Year:

2020

File:

PDF, 1.23 MB

2020

7

Sa.62. High Frequency of Long-Range SNP Identity for Founder Chromosomes Across the MHC

Erin Baschal, Andrea Steck, Jean Jasinski, George Eisenbarth

Journal:

Clinical Immunology

Year:

2008

Language:

english

File:

PDF, 66 KB

english, 2008

8

Sa.63. Utilizing Long-range Genomic Identity to Assess Type 1A Diabetes Risk

Kelly Johnson, Erin Baschal, Jean Jasinski, George Eisenbarth

Journal:

Clinical Immunology

Year:

2008

Language:

english

File:

PDF, 57 KB

english, 2008

9

Homozygosity of the Polymorphism MICA5.1 Identifies Extreme Risk of Progression to Overt Adrenal Insufficiency among 21-Hydroxylase Antibody-Positive Patients with Type 1 Diabetes

Triolo, Taylor M., Baschal, Erin E., Armstrong, Taylor K., Toews, Carrie S., Fain, Pamela R., Rewers, Marian J., Yu, Liping, Miao, Dongmei, Eisenbarth, George S., Gottlieb, Peter A., Barker, Jennifer

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 95 KB

english, 2009

10

Extreme genetic risk for type 1A diabetes in the post-genome era

Erin E. Baschal, George S. Eisenbarth

Journal:

Journal of Autoimmunity

Year:

2008

Language:

english

File:

PDF, 334 KB

english, 2008

11

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

Haller, Gabe, McCall, Kevin, Jenkitkasemwong, Supak, Sadler, Brooke, Antunes, Lilian, Nikolov, Momchil, Whittle, Julia, Upshaw, Zachary, Shin, Jimann, Baschal, Erin, Cruchaga, Carlos, Harms, Matthew,

Journal:

Nature Communications

Year:

2018

Language:

english

File:

PDF, 839 KB

english, 2018

12

Dominant Suppression of Addison's Disease Associated with HLA-B15

Baker, Peter R., Baschal, Erin E., Fain, Pam R., Nanduri, Priyaanka, Triolo, Taylor M., Siebert, Janet C., Armstrong, Taylor K., Babu, Sunanda R., Rewers, Marian J., Gottlieb, Peter A., Barker, Jennif

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2011

Language:

english

File:

PDF, 2.02 MB

english, 2011

13

Haplotype Analysis Discriminates Genetic Risk for DR3-Associated Endocrine Autoimmunity and Helps Define Extreme Risk for Addison’s Disease

Baker, Peter R., Baschal, Erin E., Fain, Pam R., Triolo, Taylor M., Nanduri, Priyaanka, Siebert, Janet C., Armstrong, Taylor K., Babu, Sunanda R., Rewers, Marian J., Gottlieb, Peter A., Barker, Jennif

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2010

Language:

english

File:

PDF, 281 KB

english, 2010

14

Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology

Baschal, Erin E., Terhune, Elizabeth A., Wethey, Cambria I., Baschal, Robin M., Robinson, Kandice D., Cuevas, Melissa T., Pradhan, Shreyash, Sutphin, Brittan S., Taylor, Matthew R. G., Gowan, Katherin

Journal:

G3 Genes|Genome|Genetics

Year:

2018

Language:

english

File:

PDF, 1.05 MB

english, 2018

15

Defining multiple common “completely” conserved major histocompatibility complex SNP haplotypes

Erin E. Baschal, Theresa A. Aly, Jean M. Jasinski, Andrea K. Steck, Janelle A. Noble, Henry A. Erlich, George S. Eisenbarth

Journal:

Clinical Immunology

Year:

2009

Language:

english

File:

PDF, 4.21 MB

english, 2009

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