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Human Genomics
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March 17, 2026
Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndromes
Chenyang Wang, Hengyuan Zhang, Meiying Wang, et al.
Human Genomics
|
May 20, 2026
The diabetes exposome: interplay of environmental and genetic determinants in diabetes
Bushra Zia, Juma AlKaabi, Adnan Agha, et al.
Human Genomics
|
June 4, 2026
Linking childhood interstitial lung disease to IARS-related disorder: clinical and preliminary functional studies in four new cases
Dan Dai, Weitao Zhou, Gaoli Jiang, et al.
Human Genomics
|
May 1, 2026
Inherited TBX4 frameshifting variants predicted to escape nonsense mediated decay in two families with variable phenotypes, including lethal lung developmental disorders
Shruti A Pande, Hiuling Chan Joiner, Przemyslaw Szafranski, et al.
Human Genomics
|
May 8, 2026
Characterizing MEFV gene variants in Jordanian patients with Familial Mediterranean Fever
Wissam A Alwazani, Nisreen A Fuqaha, Zekrayat Medras, et al.
Human Genomics
|
May 8, 2026
SLC26A2 as a key regulator and therapeutic target in hepatocellular carcinoma: evidence from pan-cancer and mechanistic studies
Rui Wang, Xijie Zhang, Bo Ren, et al.
Human Genomics
|
May 14, 2026
Differences in miRNAs profile in pregnant women with preeclampsia compared with healthy pregnant women
Vorapong Phupong, Natthaya Chuaypen, Supawadee Mingmongkol, et al.
Human Genomics
|
February 27, 2026
Genetic variations in AAK1 and ADAM17 associated with circulatory cytokines changes influence COVID-19 susceptibility and severity
Amal Bouzid, Noha M Elemam, Habiba Alsafar, et al.
Human Genomics
|
March 11, 2026
Leveraging proteomics and machine learning for mechanism and biomarker discovery on glioma progression and transformation: from LGG to GBM
Qinhong Huang, Hui Liang, Jie Liu, et al.
Human Genomics
|
February 25, 2026
Challenges in functional validation and mechanistic interpretation of a novel LACC1 variant in familial juvenile arthritis
Lin Yu, DuJiang Yang, Zhijun Ye, et al.
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of 125
Search research articles
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Showing results (181-190 of 1,250) with videos related to
Sort By:
Page
of 125
Human Genomics
|
March 17, 2026
Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndromes
Chenyang Wang, Hengyuan Zhang, Meiying Wang, et al.
Human Genomics
|
May 20, 2026
The diabetes exposome: interplay of environmental and genetic determinants in diabetes
Bushra Zia, Juma AlKaabi, Adnan Agha, et al.
Human Genomics
|
June 4, 2026
Linking childhood interstitial lung disease to IARS-related disorder: clinical and preliminary functional studies in four new cases
Dan Dai, Weitao Zhou, Gaoli Jiang, et al.
Human Genomics
|
May 1, 2026
Inherited TBX4 frameshifting variants predicted to escape nonsense mediated decay in two families with variable phenotypes, including lethal lung developmental disorders
Shruti A Pande, Hiuling Chan Joiner, Przemyslaw Szafranski, et al.
Human Genomics
|
May 8, 2026
Characterizing MEFV gene variants in Jordanian patients with Familial Mediterranean Fever
Wissam A Alwazani, Nisreen A Fuqaha, Zekrayat Medras, et al.
Human Genomics
|
May 8, 2026
SLC26A2 as a key regulator and therapeutic target in hepatocellular carcinoma: evidence from pan-cancer and mechanistic studies
Rui Wang, Xijie Zhang, Bo Ren, et al.
Human Genomics
|
May 14, 2026
Differences in miRNAs profile in pregnant women with preeclampsia compared with healthy pregnant women
Vorapong Phupong, Natthaya Chuaypen, Supawadee Mingmongkol, et al.
Human Genomics
|
February 27, 2026
Genetic variations in AAK1 and ADAM17 associated with circulatory cytokines changes influence COVID-19 susceptibility and severity
Amal Bouzid, Noha M Elemam, Habiba Alsafar, et al.
Human Genomics
|
March 11, 2026
Leveraging proteomics and machine learning for mechanism and biomarker discovery on glioma progression and transformation: from LGG to GBM
Qinhong Huang, Hui Liang, Jie Liu, et al.
Human Genomics
|
February 25, 2026
Challenges in functional validation and mechanistic interpretation of a novel LACC1 variant in familial juvenile arthritis
Lin Yu, DuJiang Yang, Zhijun Ye, et al.
Page
of 125