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Biochimica Et Biophysica Acta
|
February 14, 1992
Identification of several cyclosporine binding proteins in lymphoid and non-lymphoid cells in vivo
B M Foxwell, G Woerly, H Husi, et al.
Plos Genetics
|
September 7, 2013
The enhancer landscape during early neocortical development reveals patterns of dense regulation and co-option
Aaron M Wenger, Shoa L Clarke, James H Notwell, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2018
An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease
Heidi I Chen, Karthik A Jagadeesh, Johannes Birgmeier, et al.
Nature Biotechnology
|
May 4, 2010
GREAT improves functional interpretation of cis-regulatory regions
Cory Y McLean, Dave Bristor, Michael Hiller, et al.
Microorganisms
|
November 11, 2022
Efficacy of a Probiotic and Herbal Supplement in Models of Lung Inflammation
Nancy M Wenger, Luhua Qiao, Teodora Nicola, et al.
Schweizer Archiv Fur Tierheilkunde
|
October 7, 2016
Unexplained bleeding as primary clinical complaint in dogs infected with Angiostrongylus vasorum
T Glaus, N Sigrist, N Hofer-Inteeworn, et al.
Nature Genetics
|
November 8, 2016
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
Karthik A Jagadeesh, Aaron M Wenger, Mark J Berger, et al.
Human Mutation
|
April 13, 2012
A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb
Tobias Laurell, Julia E Vandermeer, Aaron M Wenger, et al.
Clinical Drug Investigation
|
August 18, 2023
Avacopan, a Novel Competitive C5a Receptor Antagonist, for Severe Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Ivan D Nguyen, Evan S Sinnathamby, Joseph Mason, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2018
Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome
Johannes Birgmeier, Edward D Esplin, Karthik A Jagadeesh, et al.
Page
of 17
Search research articles
Search
Showing results (101-110 of 166) with videos related to
Sort By:
Page
of 17
Biochimica Et Biophysica Acta
|
February 14, 1992
Identification of several cyclosporine binding proteins in lymphoid and non-lymphoid cells in vivo
B M Foxwell, G Woerly, H Husi, et al.
Plos Genetics
|
September 7, 2013
The enhancer landscape during early neocortical development reveals patterns of dense regulation and co-option
Aaron M Wenger, Shoa L Clarke, James H Notwell, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2018
An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease
Heidi I Chen, Karthik A Jagadeesh, Johannes Birgmeier, et al.
Nature Biotechnology
|
May 4, 2010
GREAT improves functional interpretation of cis-regulatory regions
Cory Y McLean, Dave Bristor, Michael Hiller, et al.
Microorganisms
|
November 11, 2022
Efficacy of a Probiotic and Herbal Supplement in Models of Lung Inflammation
Nancy M Wenger, Luhua Qiao, Teodora Nicola, et al.
Schweizer Archiv Fur Tierheilkunde
|
October 7, 2016
Unexplained bleeding as primary clinical complaint in dogs infected with Angiostrongylus vasorum
T Glaus, N Sigrist, N Hofer-Inteeworn, et al.
Nature Genetics
|
November 8, 2016
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
Karthik A Jagadeesh, Aaron M Wenger, Mark J Berger, et al.
Human Mutation
|
April 13, 2012
A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb
Tobias Laurell, Julia E Vandermeer, Aaron M Wenger, et al.
Clinical Drug Investigation
|
August 18, 2023
Avacopan, a Novel Competitive C5a Receptor Antagonist, for Severe Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Ivan D Nguyen, Evan S Sinnathamby, Joseph Mason, et al.
American Journal of Medical Genetics. Part A
|
March 26, 2018
Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome
Johannes Birgmeier, Edward D Esplin, Karthik A Jagadeesh, et al.
Page
of 17