Cloning and characterization of the termination site tI for the gene int transcript in phage lambda

Unraveling the intersection of aging and Parkinson's disease: a collaborative roadmap for advancing research models.

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Predator-labeling effect on byssus production in marine mussels Perna viridis (L.) and Brachidontes variabilis (Krauss).

Journal of chemical ecology·2006

Netrin receptor deficient mice exhibit functional reorganization of dopaminergic systems and do not sensitize to amphetamine.

Molecular psychiatry·2004

Naturally occurring sequence polymorphisms within HIV type 1 group O protease.

AIDS research and human retroviruses·2001

[Human clone or a delayed twin?].

Medycyna wieku rozwojowego·2001

The MLK family mediates c-Jun N-terminal kinase activation in neuronal apoptosis.

Molecular and cellular biology·2001

ZmMYC7 negatively regulates salt tolerance in maize through ZmMAPK3-mediated phosphorylation-dependent proteasomal degradation.

Gene·2026

Neuronal Prps is required for synaptic development and motor function in Drosophila melanogaster.

Gene·2026

RPA3 regulates NSCLC malignant phenotypes through epistatic functional association between GPR87 and p53.

Gene·2026

CLIC3 promotes lung cancer cell proliferation by regulating intracellular chloride and ROS levels.

Gene·2026

Detection and structural characterization of bat-associated dengue virus serotype 2: A country-level first detection in Pakistan.

Gene·2026

Progress on gibberellin-mediated regulatory networks in apple anthocyanin biosynthesis.

Gene·2026

Father-Son Comparison of Reproductive Traits.

Andrology·2026

Pediatric Gastric GIST With SDHA Truncation Despite Retained SDHB Staining: A Case Report.

Journal of pediatric hematology/oncology·2026

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Frontiers in genetics·2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Frontiers in genetics·2026

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Developmental biology·2026

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Journal of neural transmission (Vienna, Austria : 1996)·2026

Related Experiment Videos

Cloning and characterization of the termination site tI for the gene int transcript in phage lambda

Related Concept Videos

Unraveling the intersection of aging and Parkinson's disease: a collaborative roadmap for advancing research models.

Predator-labeling effect on byssus production in marine mussels Perna viridis (L.) and Brachidontes variabilis (Krauss).

Netrin receptor deficient mice exhibit functional reorganization of dopaminergic systems and do not sensitize to amphetamine.

Naturally occurring sequence polymorphisms within HIV type 1 group O protease.

[Human clone or a delayed twin?].

The MLK family mediates c-Jun N-terminal kinase activation in neuronal apoptosis.

ZmMYC7 negatively regulates salt tolerance in maize through ZmMAPK3-mediated phosphorylation-dependent proteasomal degradation.

Neuronal Prps is required for synaptic development and motor function in Drosophila melanogaster.

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CLIC3 promotes lung cancer cell proliferation by regulating intracellular chloride and ROS levels.

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Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

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Cloning and characterization of the termination site tI for the gene int transcript in phage lambda

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