Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1)

Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome.

Nature medicine·2022

Thermodynamic and structural effect of urea and guanidine chloride on the helical and on a hairpin fragment of GB1 from molecular simulations.

Proteins·2017

New quality measure for SNP array based CNV detection.

Bioinformatics (Oxford, England)·2016

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.

Molecular psychiatry·2016

16p11.2 Locus modulates response to satiety before the onset of obesity.

International journal of obesity (2005)·2015

Individual differences in impulsive action and dopamine transporter function in rat orbitofrontal cortex.

Neuroscience·2015

Sparsomycin inhibits translation through a conserved mechanism across all domains of life.

Nucleic acids research·2026

Crystal structures of type T archaeal ribonuclease P Rpp30, Rpp30/Pop5, and L7Ae provide insights into a reduced RNase P.

Nucleic acids research·2026

Partitioning of parental histones between leading and lagging strands is modulated by DNA polymerase dosage.

Nucleic acids research·2026

RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases.

Nucleic acids research·2026

A CRISPR/Cas9-induced blunt-end telomere system in S. pombe reveals RNase H2-dependent RNA primer removal at the terminal Okazaki fragment of lagging telomeres.

Nucleic acids research·2026

ZNF512B associates with mitotic spindles, regulates metaphase exit, and is crucial for stem cell differentiation.

Nucleic acids research·2026

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

Related Experiment Videos

Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1)

Related Concept Videos

Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome.

Thermodynamic and structural effect of urea and guanidine chloride on the helical and on a hairpin fragment of GB1 from molecular simulations.

New quality measure for SNP array based CNV detection.

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.

16p11.2 Locus modulates response to satiety before the onset of obesity.

Individual differences in impulsive action and dopamine transporter function in rat orbitofrontal cortex.

Sparsomycin inhibits translation through a conserved mechanism across all domains of life.

Crystal structures of type T archaeal ribonuclease P Rpp30, Rpp30/Pop5, and L7Ae provide insights into a reduced RNase P.

Partitioning of parental histones between leading and lagging strands is modulated by DNA polymerase dosage.

RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases.

A CRISPR/Cas9-induced blunt-end telomere system in S. pombe reveals RNase H2-dependent RNA primer removal at the terminal Okazaki fragment of lagging telomeres.

ZNF512B associates with mitotic spindles, regulates metaphase exit, and is crucial for stem cell differentiation.

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Related Experiment Videos

Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1)

Related Concept Videos

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