Localization of the mouse gene encoding tyrosine kinase receptor type 10 on distal chromosome 1

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Journal of dental research·2019

Military assistance to the civil authority: medical liaison with the Manchester clinicians after the Arena bombing.

BMJ military health·2018

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.

Clinical genetics·2017

Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.

Clinical genetics·2016

Improving rehabilitation after critical illness through outpatient physiotherapy classes and essential amino acid supplement: A randomized controlled trial.

Journal of critical care·2015

Genome-wide methylation analysis in Silver-Russell syndrome patients.

Human genetics·2015

USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Genomic analysis of breed composition and population structure in Montana composite cattle.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Metabolic convergence of diabetes and prostate cancer: from dysglycemia to tumor microenvironment reprogramming.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Generation of miR-141/200c conditional knockout mice from knockout-first, reporter-tagged parent and functional validation of the floxed allele.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Machine learning identifies ac4C-related prognostic signature and TUBA1C as therapeutic target in COAD.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Delving into the clinical and genetic spectrum of NLSDM: A case study.

Journal of neuromuscular diseases·2026

Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy.

Molecular genetics & genomic medicine·2026

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Neurogenetics·2026

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Medicine·2026

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine·2026

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Medicine·2026

Related Experiment Videos

Localization of the mouse gene encoding tyrosine kinase receptor type 10 on distal chromosome 1

Related Concept Videos

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Military assistance to the civil authority: medical liaison with the Manchester clinicians after the Arena bombing.

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.

Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.

Improving rehabilitation after critical illness through outpatient physiotherapy classes and essential amino acid supplement: A randomized controlled trial.

Genome-wide methylation analysis in Silver-Russell syndrome patients.

USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Genomic analysis of breed composition and population structure in Montana composite cattle.

Metabolic convergence of diabetes and prostate cancer: from dysglycemia to tumor microenvironment reprogramming.

Generation of miR-141/200c conditional knockout mice from knockout-first, reporter-tagged parent and functional validation of the floxed allele.

Machine learning identifies ac4C-related prognostic signature and TUBA1C as therapeutic target in COAD.

Delving into the clinical and genetic spectrum of NLSDM: A case study.

Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy.

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Related Experiment Videos

Localization of the mouse gene encoding tyrosine kinase receptor type 10 on distal chromosome 1

Related Concept Videos

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