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FTO demethylase activity is essential for normal bone growth and bone mineralization in mice';

FTO demethylase activity is essential for normal bone growth and bone mineralization in mice

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Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis';

Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis

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An N-ethyl-N-nitrosourea (ENU)-induced Tyr265Stop mutation of the DNA polymerase accessory subunit gamma 2 (Polg2) is associated with renal calcification in mice';

An N-ethyl-N-nitrosourea (ENU)-induced Tyr265Stop mutation of the DNA polymerase accessory subunit gamma 2 (Polg2) is associated with renal calcification in mice

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ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling';

ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling

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Helios is a key transcriptional regulator of outer hair cell maturation';

Helios is a key transcriptional regulator of outer hair cell maturation

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High-resolution muCT of a mouse embryo using a compact laser-driven X-ray betatron source';

High-resolution muCT of a mouse embryo using a compact laser-driven X-ray betatron source

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A genetic modifier suggests that endurance exercise exacerbates Huntington’s Disease';

A genetic modifier suggests that endurance exercise exacerbates Huntington’s Disease

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Leukemia Inhibitory Factor-Receptor is Dispensable for Prenatal Testis Development but is Required in Sertoli cells for Normal Spermatogenesis in Mice';

Leukemia Inhibitory Factor-Receptor is Dispensable for Prenatal Testis Development but is Required in Sertoli cells for Normal Spermatogenesis in Mice

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Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function';

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function

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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features';

Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features

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