Isolation and mapping of a polymorphic DNA sequence (pCMM63) on chromosome 2 [D2S51]

Growth and morphogenesis in Streptomyces.

FEMS microbiology letters·1992

Malignant lymphoma in a patient with relapsing bronchiolitis obliterans organizing pneumonia.

Chest·1992

Pharmacokinetics and tissue penetration of a single dose of ceftriaxone (1,000 milligrams intravenously) for antibiotic prophylaxis in thoracic surgery.

Antimicrobial agents and chemotherapy·1992

Safety of interventional rigid bronchoscopy using intravenous anesthesia and spontaneous assisted ventilation. A prospective study.

Chest·1992

Relatedness of penicillin-binding protein 1a genes from different clones of penicillin-resistant Streptococcus pneumoniae isolated in South Africa and Spain.

The EMBO journal·1992

Nucleotide sequence of the nfaA gene encoding the antigen 8786 adhesive factor of enterotoxigenic Escherichia coli.

FEMS microbiology letters·1992

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

Nucleic acids research·2026

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

Nucleic acids research·2026

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

Nucleic acids research·2026

The leading region of many plasmids is adapted for translational efficiency.

Nucleic acids research·2026

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

Nucleic acids research·2026

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Nucleic acids research·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (pCMM63) on chromosome 2 [D2S51]

Related Concept Videos

Growth and morphogenesis in Streptomyces.

Malignant lymphoma in a patient with relapsing bronchiolitis obliterans organizing pneumonia.

Pharmacokinetics and tissue penetration of a single dose of ceftriaxone (1,000 milligrams intravenously) for antibiotic prophylaxis in thoracic surgery.

Safety of interventional rigid bronchoscopy using intravenous anesthesia and spontaneous assisted ventilation. A prospective study.

Relatedness of penicillin-binding protein 1a genes from different clones of penicillin-resistant Streptococcus pneumoniae isolated in South Africa and Spain.

Nucleotide sequence of the nfaA gene encoding the antigen 8786 adhesive factor of enterotoxigenic Escherichia coli.

Nuclear receptor Nur77 resolves the inflammatory response of macrophages primarily by regulating expression of AP-1 transcription factors and their target genes.

When circular RNAs meet the genome: CiR-loops as chromatin regulators and disease drivers.

SpliceImpactR maps alternative RNA processing events driving protein functional diversity.

The leading region of many plasmids is adapted for translational efficiency.

Binary-SPA: a reference-free method for cell annotation in high-resolution spatial transcriptomics.

DeepPNI: a language- and graph-based model for mutation-driven protein-nucleic acid binding energetics.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

Isolation and mapping of a polymorphic DNA sequence (pCMM63) on chromosome 2 [D2S51]

Related Concept Videos

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