GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region

Identification of the Novel Tooth-Specific Transcription Factor AmeloD.

Journal of dental research·2018

SU-E-T-600: Utilizing Collimator Rotation to Increase Maximum Treatable Target Dimensions Using an Elekta Synergy-S with Beam Modulator Multileaf Collimator.

Medical physics·2017

IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.

Clinical genetics·2015

Functional Significance of MMP3 and TIMP2 Polymorphisms in Cleft Lip/Palate.

Journal of dental research·2014

Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot.

American journal of medical genetics. Part A·2012

Association of AXIN2 with non-syndromic oral clefts in multiple populations.

Journal of dental research·2012

CpG content contributes to tissue-resident macrophage enhancer selection.

Nucleic acids research·2026

L Antigen Family Member 3 stabilizes stalled replication forks by reducing MRE11 resection to maintain genome stability.

Nucleic acids research·2026

A single-cell transcriptome atlas reveals paradoxical monoallelic expression of RNA editing and heterozygous SNPs.

Nucleic acids research·2026

Assembly of exon junction complexes on spliceosomes begins before spliceosome activation.

Nucleic acids research·2026

CompBio and MIRaS-a multi-omic analysis platform built on a memory-based intelligence engine.

Nucleic acids research·2026

Distinguishing self from non-self RNA by editing-specific inosine patterns.

Nucleic acids research·2026

Primary glioblastoma with spontaneous transdural invasion and contiguous calvarial/mastoid osteolysis: a case report and literature review.

Frontiers in surgery·2026

Integrating deep learning and pangenomics to recover missing heritability from wild structural variations.

BMC genomics·2026

Genomic analysis of an Arctic marine Tenacibaculum sp. SM2510 reveals its genetic potential for glutathione utilization.

Marine genomics·2026

Lactiplantibacillus plantarum: Systems Biology of a Versatile Microbe.

Probiotics and antimicrobial proteins·2026

Proteogenomics in human populations.

Nature reviews. Genetics·2026

Whole Exome Sequencing Unveils Novel Pathogenic Variants in an Iranian Cohort with Retinal Dystrophies: Implications for Genetic Diagnosis and Counseling.

Molecular and cellular probes·2026

Related Experiment Videos

GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region

Related Concept Videos

Identification of the Novel Tooth-Specific Transcription Factor AmeloD.

SU-E-T-600: Utilizing Collimator Rotation to Increase Maximum Treatable Target Dimensions Using an Elekta Synergy-S with Beam Modulator Multileaf Collimator.

IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 families.

Functional Significance of MMP3 and TIMP2 Polymorphisms in Cleft Lip/Palate.

Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot.

Association of AXIN2 with non-syndromic oral clefts in multiple populations.

CpG content contributes to tissue-resident macrophage enhancer selection.

L Antigen Family Member 3 stabilizes stalled replication forks by reducing MRE11 resection to maintain genome stability.

A single-cell transcriptome atlas reveals paradoxical monoallelic expression of RNA editing and heterozygous SNPs.

Assembly of exon junction complexes on spliceosomes begins before spliceosome activation.

CompBio and MIRaS-a multi-omic analysis platform built on a memory-based intelligence engine.

Distinguishing self from non-self RNA by editing-specific inosine patterns.

Primary glioblastoma with spontaneous transdural invasion and contiguous calvarial/mastoid osteolysis: a case report and literature review.

Integrating deep learning and pangenomics to recover missing heritability from wild structural variations.

Genomic analysis of an Arctic marine Tenacibaculum sp. SM2510 reveals its genetic potential for glutathione utilization.

Lactiplantibacillus plantarum: Systems Biology of a Versatile Microbe.

Proteogenomics in human populations.

Whole Exome Sequencing Unveils Novel Pathogenic Variants in an Iranian Cohort with Retinal Dystrophies: Implications for Genetic Diagnosis and Counseling.

Related Experiment Videos

GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region

Related Concept Videos

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