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Human Mutation
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April 30, 2014
A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form
Julia E VanderMeer, Reymundo Lozano, Miao Sun, et al.
Blood Advances
|
June 17, 2020
Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders
Vanessa Gadoury-Levesque, Lei Dong, Rui Su, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
February 8, 2005
[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family]
Xiu-li Zhao, Jin-ping Meng, Miao Sun, et al.
Parasites & Vectors
|
February 24, 2017
Fasciolopsis buski (Digenea: Fasciolidae) from China and India may represent distinct taxa based on mitochondrial and nuclear ribosomal DNA sequences
Jun Ma, Miao-Miao Sun, Jun-Jun He, et al.
Nature Communications
|
July 5, 2020
Recent accelerated diversification in rosids occurred outside the tropics
Miao Sun, Ryan A Folk, Matthew A Gitzendanner, et al.
Horticulture Research
|
July 9, 2020
Germplasm resources and genetic breeding of <i>Paeonia</i>: a systematic review
Yong Yang, Miao Sun, Shanshan Li, et al.
Iscience
|
July 24, 2024
Loss of the polarity protein Par3 promotes dendritic spine neoteny and enhances learning and memory
Mikayla M Voglewede, Elif Naz Ozsen, Noah Ivak, et al.
American Journal of Botany
|
June 11, 2020
Estimating rates and patterns of diversification with incomplete sampling: a case study in the rosids
Miao Sun, Ryan A Folk, Matthew A Gitzendanner, et al.
Horticulture Research
|
April 16, 2025
Advances in the study of senescence mechanisms in the genus <i>Paeonia</i>
Yuxuan Wang, Miao Sun, Wei Zhu, et al.
The Journal of Clinical Investigation
|
December 21, 2013
Huntingtin-associated protein 1 regulates postnatal neurogenesis and neurotrophin receptor sorting
Jianxing Xiang, Hao Yang, Ting Zhao, et al.
Page
of 66
Search research articles
Search
Showing results (361-370 of 652) with videos related to
Sort By:
Page
of 66
Human Mutation
|
April 30, 2014
A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form
Julia E VanderMeer, Reymundo Lozano, Miao Sun, et al.
Blood Advances
|
June 17, 2020
Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders
Vanessa Gadoury-Levesque, Lei Dong, Rui Su, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
February 8, 2005
[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family]
Xiu-li Zhao, Jin-ping Meng, Miao Sun, et al.
Parasites & Vectors
|
February 24, 2017
Fasciolopsis buski (Digenea: Fasciolidae) from China and India may represent distinct taxa based on mitochondrial and nuclear ribosomal DNA sequences
Jun Ma, Miao-Miao Sun, Jun-Jun He, et al.
Nature Communications
|
July 5, 2020
Recent accelerated diversification in rosids occurred outside the tropics
Miao Sun, Ryan A Folk, Matthew A Gitzendanner, et al.
Horticulture Research
|
July 9, 2020
Germplasm resources and genetic breeding of <i>Paeonia</i>: a systematic review
Yong Yang, Miao Sun, Shanshan Li, et al.
Iscience
|
July 24, 2024
Loss of the polarity protein Par3 promotes dendritic spine neoteny and enhances learning and memory
Mikayla M Voglewede, Elif Naz Ozsen, Noah Ivak, et al.
American Journal of Botany
|
June 11, 2020
Estimating rates and patterns of diversification with incomplete sampling: a case study in the rosids
Miao Sun, Ryan A Folk, Matthew A Gitzendanner, et al.
Horticulture Research
|
April 16, 2025
Advances in the study of senescence mechanisms in the genus <i>Paeonia</i>
Yuxuan Wang, Miao Sun, Wei Zhu, et al.
The Journal of Clinical Investigation
|
December 21, 2013
Huntingtin-associated protein 1 regulates postnatal neurogenesis and neurotrophin receptor sorting
Jianxing Xiang, Hao Yang, Ting Zhao, et al.
Page
of 66