TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1)

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

Large-scale mutational analysis uncovers molecular mechanisms governing dual RNA functions in transposons.

Nucleic acids research·2026

Temporal dynamics of intragenic enhancer RNAs regulate Lin28a expression in response to external stimuli in embryonic stem cells.

Nucleic acids research·2026

PCNA-RECQL5-RPRD1B recruit repair components to stressed replication forks to promote survival of BRCA1-deficient cancer cells.

Nucleic acids research·2026

Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis.

Nucleic acids research·2026

PCRD-seq: proximity crosslinking-induced RNA depletion sequencing for low-input chromatin-associated transcriptome profiling.

Nucleic acids research·2026

Modeling conformational transitions in DNA, RNA, and protein-nucleic acid complexes.

Nucleic acids research·2026

Debating the Delphi View of Dyslexia: A Response to Metsala, Morsanyi and Colleagues.

Dyslexia (Chichester, England)·2026

Practice Patterns of Speech-Language Pathologists for Vocal Fold Paresis.

Journal of voice : official journal of the Voice Foundation·2026

Lipoid Proteinosis with Homozygous ECM1 c.507del Variant and Functionally Significant Eyelid Involvement: A Case Report.

Clinical, cosmetic and investigational dermatology·2026

The burden of Lipoprotein(a) [Lp(a)] in Africa: A systematic review.

PloS one·2026

'If You Don't Speak Up, It Will Eat You Up': A Critical Discourse Analysis of Voice and Silence in a Multicultural Clinical Healthcare System.

Nursing inquiry·2026

Quality Evaluation Using the Mobile App Rating Scale for Speech Therapy in Parkinson Disease: Systematic Search and Evaluation.

JMIR formative research·2026

Related Experiment Videos

TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1)

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.

Large-scale mutational analysis uncovers molecular mechanisms governing dual RNA functions in transposons.

Temporal dynamics of intragenic enhancer RNAs regulate Lin28a expression in response to external stimuli in embryonic stem cells.

PCNA-RECQL5-RPRD1B recruit repair components to stressed replication forks to promote survival of BRCA1-deficient cancer cells.

Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis.

PCRD-seq: proximity crosslinking-induced RNA depletion sequencing for low-input chromatin-associated transcriptome profiling.

Modeling conformational transitions in DNA, RNA, and protein-nucleic acid complexes.

Debating the Delphi View of Dyslexia: A Response to Metsala, Morsanyi and Colleagues.

Practice Patterns of Speech-Language Pathologists for Vocal Fold Paresis.

Lipoid Proteinosis with Homozygous ECM1 c.507del Variant and Functionally Significant Eyelid Involvement: A Case Report.

The burden of Lipoprotein(a) [Lp(a)] in Africa: A systematic review.

'If You Don't Speak Up, It Will Eat You Up': A Critical Discourse Analysis of Voice and Silence in a Multicultural Clinical Healthcare System.

Quality Evaluation Using the Mobile App Rating Scale for Speech Therapy in Parkinson Disease: Systematic Search and Evaluation.

Related Experiment Videos

TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1)

Related Concept Videos

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