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EMBO Molecular Medicine
|
October 15, 2019
Targeting TGFβR2-mutant tumors exposes vulnerabilities to stromal TGFβ blockade in pancreatic cancer
Huocong Huang, Yuqing Zhang, Valerie Gallegos, et al.
BMC Medical Genetics
|
February 23, 2020
Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene
Nida S Iqbal, Thomas A Jascur, Steven M Harrison, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 21, 2021
A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy
Min Ni, Bushra Afroze, Chao Xing, et al.
Human Genetics
|
April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes
Lane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 10, 2019
A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud
Caixia Xu, Xiaoming Yang, Hang Zhou, et al.
Diabetes
|
September 8, 2017
Hepatic GALE Regulates Whole-Body Glucose Homeostasis by Modulating <i>Tff3</i> Expression
Yi Zhu, Shangang Zhao, Yingfeng Deng, et al.
Cell Reports
|
June 25, 2013
An iPSC line from human pancreatic ductal adenocarcinoma undergoes early to invasive stages of pancreatic cancer progression
Jungsun Kim, John P Hoffman, R Katherine Alpaugh, et al.
Cell Research
|
September 3, 2025
Targeting necrotic lipid release in tumors enhances immunosurveillance and cancer immunotherapy of glioblastoma
Yapeng Ji, Junyao Jiang, Lei Hu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 28, 2020
Forward genetic analysis using OCT screening identifies <i>Sfxn3</i> mutations leading to progressive outer retinal degeneration in mice
Bo Chen, Bogale Aredo, Yi Ding, et al.
Human Mutation
|
June 4, 2021
Biallelic variants in RNU12 cause CDAGS syndrome
Chao Xing, Mohammed Kanchwala, Jonathan J Rios, et al.
Page
of 54
Search research articles
Search
Showing results (461-470 of 535) with videos related to
Sort By:
Page
of 54
EMBO Molecular Medicine
|
October 15, 2019
Targeting TGFβR2-mutant tumors exposes vulnerabilities to stromal TGFβ blockade in pancreatic cancer
Huocong Huang, Yuqing Zhang, Valerie Gallegos, et al.
BMC Medical Genetics
|
February 23, 2020
Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene
Nida S Iqbal, Thomas A Jascur, Steven M Harrison, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 21, 2021
A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy
Min Ni, Bushra Afroze, Chao Xing, et al.
Human Genetics
|
April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes
Lane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 10, 2019
A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud
Caixia Xu, Xiaoming Yang, Hang Zhou, et al.
Diabetes
|
September 8, 2017
Hepatic GALE Regulates Whole-Body Glucose Homeostasis by Modulating <i>Tff3</i> Expression
Yi Zhu, Shangang Zhao, Yingfeng Deng, et al.
Cell Reports
|
June 25, 2013
An iPSC line from human pancreatic ductal adenocarcinoma undergoes early to invasive stages of pancreatic cancer progression
Jungsun Kim, John P Hoffman, R Katherine Alpaugh, et al.
Cell Research
|
September 3, 2025
Targeting necrotic lipid release in tumors enhances immunosurveillance and cancer immunotherapy of glioblastoma
Yapeng Ji, Junyao Jiang, Lei Hu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 28, 2020
Forward genetic analysis using OCT screening identifies <i>Sfxn3</i> mutations leading to progressive outer retinal degeneration in mice
Bo Chen, Bogale Aredo, Yi Ding, et al.
Human Mutation
|
June 4, 2021
Biallelic variants in RNU12 cause CDAGS syndrome
Chao Xing, Mohammed Kanchwala, Jonathan J Rios, et al.
Page
of 54