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Plos Genetics
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March 12, 2016
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene
Kerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, et al.
Psychiatric Genetics
|
September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2
Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, et al.
Experimental Dermatology
|
June 17, 2016
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2
Johannes Fischer, Franziska Degenhardt, Andrea Hofmann, et al.
The Journal of Investigative Dermatology
|
October 30, 2017
Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata
Aylar Tafazzoli, Andreas J Forstner, David Broadley, et al.
Nature Immunology
|
March 8, 2016
Tumor-necrosis factor impairs CD4(+) T cell-mediated immunological control in chronic viral infection
Marc Beyer, Zeinab Abdullah, Jens M Chemnitz, et al.
Nature Immunology
|
July 5, 2020
Publisher Correction: Tumor-necrosis factor impairs CD4<sup>+</sup> T cell-mediated immunological control in chronic viral infection
Marc Beyer, Zeinab Abdullah, Jens M Chemnitz, et al.
International Journal of Cancer
|
September 16, 2014
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis
Sukanya Horpaopan, Isabel Spier, Alexander M Zink, et al.
American Journal of Human Genetics
|
March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
Elisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.
Nature Immunology
|
August 16, 2011
Repression of the genome organizer SATB1 in regulatory T cells is required for suppressive function and inhibition of effector differentiation
Marc Beyer, Yasser Thabet, Roman-Ulrich Müller, et al.
Nature Genetics
|
March 15, 2016
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci
David Ellinghaus, Luke Jostins, Sarah L Spain, et al.
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of 7
Search research articles
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Showing results (51-60 of 68) with videos related to
Sort By:
Page
of 7
Plos Genetics
|
March 12, 2016
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene
Kerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, et al.
Psychiatric Genetics
|
September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2
Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, et al.
Experimental Dermatology
|
June 17, 2016
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2
Johannes Fischer, Franziska Degenhardt, Andrea Hofmann, et al.
The Journal of Investigative Dermatology
|
October 30, 2017
Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata
Aylar Tafazzoli, Andreas J Forstner, David Broadley, et al.
Nature Immunology
|
March 8, 2016
Tumor-necrosis factor impairs CD4(+) T cell-mediated immunological control in chronic viral infection
Marc Beyer, Zeinab Abdullah, Jens M Chemnitz, et al.
Nature Immunology
|
July 5, 2020
Publisher Correction: Tumor-necrosis factor impairs CD4<sup>+</sup> T cell-mediated immunological control in chronic viral infection
Marc Beyer, Zeinab Abdullah, Jens M Chemnitz, et al.
International Journal of Cancer
|
September 16, 2014
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis
Sukanya Horpaopan, Isabel Spier, Alexander M Zink, et al.
American Journal of Human Genetics
|
March 29, 2016
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
Elisabeth Mangold, Anne C Böhmer, Nina Ishorst, et al.
Nature Immunology
|
August 16, 2011
Repression of the genome organizer SATB1 in regulatory T cells is required for suppressive function and inhibition of effector differentiation
Marc Beyer, Yasser Thabet, Roman-Ulrich Müller, et al.
Nature Genetics
|
March 15, 2016
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci
David Ellinghaus, Luke Jostins, Sarah L Spain, et al.
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of 7