A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26]

Multimorbidity in adolescents in sub-Saharan Africa: a systematic review.

Communications medicine·2026

Growth performance, efficiency, and composition of Holstein heifers fed 2 levels of nutrient intake from 44 to 350 kilograms body weight.

Journal of dairy science·2026

Public health and military health.

Journal of public health (Oxford, England)·2022

Formulating diets for intestinal unavailable nitrogen using blood meal in high-producing dairy cattle.

Journal of dairy science·2022

The postpartum abdomen: psychology, surgery and quality of life.

Hernia : the journal of hernias and abdominal wall surgery·2021

Establishing communicable disease surveillance systems.

BMJ military health·2021

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

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26]

Related Concept Videos

Multimorbidity in adolescents in sub-Saharan Africa: a systematic review.

Growth performance, efficiency, and composition of Holstein heifers fed 2 levels of nutrient intake from 44 to 350 kilograms body weight.

Public health and military health.

Formulating diets for intestinal unavailable nitrogen using blood meal in high-producing dairy cattle.

The postpartum abdomen: psychology, surgery and quality of life.

Establishing communicable disease surveillance systems.

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.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26]

Related Concept Videos

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