Genetic studies: look no further than your own backyard

Scaling up self-assembly: bottom-up approaches to macroscopic particle organization.

Soft matter·2015

Ambient hypoxia enhances the loss of muscle mass after extensive injury.

Pflugers Archiv : European journal of physiology·2013

Granular mixing and segregation in zigzag chute flow.

Physical review. E, Statistical, nonlinear, and soft matter physics·2013

Serum apolipoprotein C-III is independently associated with chronic hepatitis C infection and advanced fibrosis.

Hepatology international·2011

Sex and age differences in lipid response to chronic infection with the hepatitis C virus in the United States National Health and Nutrition Examination Surveys.

Journal of viral hepatitis·2010

Thermal expansion effects and heat conduction in granular materials.

Physical review. E, Statistical, nonlinear, and soft matter physics·2007

In situ programming of unconventional T cells.

Trends in biotechnology·2026

Empowering microbes with natural armor: encapsulation strategies for agri-food and biotech innovations.

Trends in biotechnology·2026

Pilot-scale production of leucine from CO2.

Trends in biotechnology·2026

Precision-fermented milk proteins as a model for industrial food biotechnology.

Trends in biotechnology·2026

Toward a 4D genome annotation of CHO cells for biomanufacturing.

Trends in biotechnology·2026

Scalable 4D biofabrication process for the manufacture of scaffold-free bone-forming callus implants.

Trends in biotechnology·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Genetic studies: look no further than your own backyard

Related Concept Videos

Scaling up self-assembly: bottom-up approaches to macroscopic particle organization.

Ambient hypoxia enhances the loss of muscle mass after extensive injury.

Granular mixing and segregation in zigzag chute flow.

Serum apolipoprotein C-III is independently associated with chronic hepatitis C infection and advanced fibrosis.

Sex and age differences in lipid response to chronic infection with the hepatitis C virus in the United States National Health and Nutrition Examination Surveys.

Thermal expansion effects and heat conduction in granular materials.

In situ programming of unconventional T cells.

Empowering microbes with natural armor: encapsulation strategies for agri-food and biotech innovations.

Pilot-scale production of leucine from CO2.

Precision-fermented milk proteins as a model for industrial food biotechnology.

Toward a 4D genome annotation of CHO cells for biomanufacturing.

Scalable 4D biofabrication process for the manufacture of scaffold-free bone-forming callus implants.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

Genetic studies: look no further than your own backyard

Related Concept Videos

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