Dinucleotide repeat polymorphism at the human poly (ADP-ribose) polymerase gene (PPOL)

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

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

The tumor suppressor menin is a key scaffold mediator for homologous recombination repair.

Nucleic acids research·2026

Duplication of specialized cis-acting elements SLI and SLIII in the viral RNA 3'UTR enables mosquito-borne orthoflavivirus adaptation to avian hosts.

Nucleic acids research·2026

Discovery and biosynthesis of a novel diaminopropane-modified thymine in phage DNA.

Nucleic acids research·2026

Ctf18-dependent localization of interstitial telomeric sequence to nuclear pore complexes prevents chromosome fragility.

Nucleic acids research·2026

Nuclear compartmentalization at the G1/S transition plays a key role in DNA replication control.

Nature communications·2026

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Animal genetics·2026

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

Kidney360·2026

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

The Journal of cell biology·2026

Related Experiment Videos

Dinucleotide repeat polymorphism at the human poly (ADP-ribose) polymerase gene (PPOL)

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.

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.

The tumor suppressor menin is a key scaffold mediator for homologous recombination repair.

Duplication of specialized cis-acting elements SLI and SLIII in the viral RNA 3'UTR enables mosquito-borne orthoflavivirus adaptation to avian hosts.

Discovery and biosynthesis of a novel diaminopropane-modified thymine in phage DNA.

Ctf18-dependent localization of interstitial telomeric sequence to nuclear pore complexes prevents chromosome fragility.

Nuclear compartmentalization at the G1/S transition plays a key role in DNA replication control.

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

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Dinucleotide repeat polymorphism at the human poly (ADP-ribose) polymerase gene (PPOL)

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