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Bone
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August 21, 2018
Osteoblast derived-neurotrophin‑3 induces cartilage removal proteases and osteoclast-mediated function at injured growth plate in rats
Yu-Wen Su, Shek Man Chim, Lin Zhou, et al.
Elife
|
December 13, 2024
Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings
Shek Man Chim, Kristen Howell, John Dronzek, et al.
Human Molecular Genetics
|
October 26, 2020
NMIHBA results from hypomorphic PRUNE1 variants that lack short-chain exopolyphosphatase activity
Harikiran Nistala, John Dronzek, Claudia Gonzaga-Jauregui, et al.
Nature Genetics
|
June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2020
Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide
Claudia Gonzaga-Jauregui, Gozde Yesil, Harikiran Nistala, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Bone
|
August 21, 2018
Osteoblast derived-neurotrophin‑3 induces cartilage removal proteases and osteoclast-mediated function at injured growth plate in rats
Yu-Wen Su, Shek Man Chim, Lin Zhou, et al.
Elife
|
December 13, 2024
Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings
Shek Man Chim, Kristen Howell, John Dronzek, et al.
Human Molecular Genetics
|
October 26, 2020
NMIHBA results from hypomorphic PRUNE1 variants that lack short-chain exopolyphosphatase activity
Harikiran Nistala, John Dronzek, Claudia Gonzaga-Jauregui, et al.
Nature Genetics
|
June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.
European Journal of Human Genetics : EJHG
|
May 8, 2020
Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide
Claudia Gonzaga-Jauregui, Gozde Yesil, Harikiran Nistala, et al.
Page
of 3