E. E. Baschal : rechercher sur Z-Library

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1

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

Année:

2006

Langue:

english

Fichier:

PDF, 3.55 MB

english, 2006

2

TheHLA-B*3906allele imparts a high risk of diabetes only on specificHLA-DR/DQhaplotypes

E. E. Baschal, P. R. Baker, K. R. Eyring, J. C. Siebert, J. M. Jasinski, G. S. Eisenbarth

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 357 KB

english, 2011

3

The frequent and conserved DR3-B8-A1 extended haplotype confers less diabetes risk than other DR3 haplotypes

E. E. Baschal, T. A. Aly, J. M. Jasinski, A. K. Steck, K. N. Johnson, J. A. Noble, H. A. Erlich, G. S. Eisenbarth, Diabetes Genetics Consortium

Journal:

Diabetes, Obesity and Metabolism

Année:

2009

Langue:

english

Fichier:

PDF, 185 KB

english, 2009

4

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

Année:

2011

Langue:

english

Fichier:

PDF, 1.14 MB

english, 2011

5

rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype

Steck, A K, Baschal, E E, Jasinski, J M, Boehm, B O, Bottini, N, Concannon, P, Julier, C, Morahan, G, Noble, J A, Polychronakos, C

Journal:

Genes and Immunity

Année:

2009

Langue:

english

Fichier:

PDF, 376 KB

english, 2009

6

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

Année:

2007

Langue:

english

Fichier:

PDF, 45 KB

english, 2007

7

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

Kelly Johnson, Erin Baschal, Jean Jasinski, George Eisenbarth

Journal:

Clinical Immunology

Année:

2008

Langue:

english

Fichier:

PDF, 57 KB

english, 2008

8

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

Année:

2008

Langue:

english

Fichier:

PDF, 66 KB

english, 2008

9

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

Année:

2009

Langue:

english

Fichier:

PDF, 4.21 MB

english, 2009

10

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

Année:

2012

Langue:

english

Fichier:

PDF, 1.26 MB

english, 2012

11

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

Erin E. Baschal, George S. Eisenbarth

Journal:

Journal of Autoimmunity

Année:

2008

Langue:

english

Fichier:

PDF, 334 KB

english, 2008

12

Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis

Baschal, E. E., Wethey, C. I., Swindle, K., Baschal, R. M., Gowan, K., Tang, N. L. S., Alvarado, D. M., Haller, G. E., Dobbs, M. B., Taylor, M. R. G., Gurnett, C. A., Jones, K. L., Miller, N. H.

Journal:

G3 Genes|Genome|Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 863 KB

english, 2015

13

Analysis of Single Nucleotide Polymorphisms Identifies Major Type 1A Diabetes Locus Telomeric of the Major Histocompatibility Complex

Aly, T. A., Baschal, E. E., Jahromi, M. M., Fernando, M. S., Babu, S. R., Fingerlin, T. E., Kretowski, A., Erlich, H. A., Fain, P. R., Rewers, M. J., Eisenbarth, G. S.

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 303 KB

english, 2008

14

HLA-DPB10402 Protects Against Type 1A Diabetes Autoimmunity in the Highest Risk DR3-DQB10201/DR4-DQB1*0302 DAISY Population

Baschal, E. E., Aly, T. A., Babu, S. R., Fernando, M. S., Yu, L., Miao, D., Barriga, K. J., Norris, J. M., Noble, J. A., Erlich, H. A., Rewers, M. J., Eisenbarth, G. S.

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 155 KB

english, 2007

15

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

Année:

2015

Langue:

english

Fichier:

PDF, 1.39 MB

english, 2015

16

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

Année:

2009

Langue:

english

Fichier:

PDF, 95 KB

english, 2009

17

Two Single Nucleotide Polymorphisms Identify the Highest-Risk Diabetes HLA Genotype: Potential for Rapid Screening

Barker, J. M., Triolo, T. M., Aly, T. A., Baschal, E. E., Babu, S. R., Kretowski, A., Rewers, M. J., Eisenbarth, G. S.

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 137 KB

english, 2008

18

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

Année:

2010

Langue:

english

Fichier:

PDF, 281 KB

english, 2010

19

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

Année:

2011

Langue:

english

Fichier:

PDF, 2.02 MB

english, 2011

20

A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis

Haller, G., Alvarado, D., McCall, K., Yang, P., Cruchaga, C., Harms, M., Goate, A., Willing, M., Morcuende, J. A., Baschal, E., Miller, N. H., Wise, C., Dobbs, M. B., Gurnett, C. A.

Journal:

Human Molecular Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 890 KB

english, 2015

21

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

Année:

2018

Langue:

english

Fichier:

PDF, 1.05 MB

english, 2018

22

A comparison of fixation methods in adolescent patients with diaphyseal forearm fractures

Freese, Krister P., Faulk, L. Wade, Palmer, Claire, Baschal, Robin M., Sibbel, Sarah E.

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 458 KB

english, 2018

23

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

Année:

2018

Langue:

english

Fichier:

PDF, 839 KB

english, 2018

24

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

Année:

2020

Fichier:

PDF, 1.23 MB

2020