Nucleotide sequence of human rho cDNA clone 12

Suppression and restoration of v-SRC expression in rsv transformed-cells after transfection with N-ras and its antagonist.

International journal of oncology·2011

Modulation of RhoA-Rho kinase-mediated Ca2+ sensitization of rabbit myometrium during pregnancy - role of Rnd3.

The Journal of physiology·2003

Rho-dependent transfer of Citron-kinase to the cleavage furrow of dividing cells.

Journal of cell science·2001

A novel group IIA phospholipase A2 interacts with v-Src oncoprotein from RSV-transformed hamster cells.

The Journal of biological chemistry·2001

Membrane targeting: what a difference a G makes.

Current biology : CB·2000

Induced expression of Rnd3 is associated with transformation of polarized epithelial cells by the Raf-MEK-extracellular signal-regulated kinase pathway.

Molecular and cellular biology·2000

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

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

Nucleotide sequence of human rho cDNA clone 12

Related Concept Videos

Suppression and restoration of v-SRC expression in rsv transformed-cells after transfection with N-ras and its antagonist.

Modulation of RhoA-Rho kinase-mediated Ca2+ sensitization of rabbit myometrium during pregnancy - role of Rnd3.

Rho-dependent transfer of Citron-kinase to the cleavage furrow of dividing cells.

A novel group IIA phospholipase A2 interacts with v-Src oncoprotein from RSV-transformed hamster cells.

Membrane targeting: what a difference a G makes.

Induced expression of Rnd3 is associated with transformation of polarized epithelial cells by the Raf-MEK-extracellular signal-regulated kinase pathway.

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.

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

Nucleotide sequence of human rho cDNA clone 12

Related Concept Videos

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