Northern blot normalization with a 28S rRNA oligonucleotide probe

Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B.

European journal of endocrinology·2009

Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?

Clinical endocrinology·2008

Simultaneous regression of Philadelphia chromosome and multiple nonrecurrent clonal chromosomal abnormalities with imatinib mesylate in a patient autografted 22 years before for chronic myelogenous leukemia.

Leukemia & lymphoma·2007

GW body disassembly triggered by siRNAs independently of their silencing activity.

Nucleic acids research·2007

The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules.

Journal of cell science·2005

Low levels of lymphocyte MDR1 gene expression during early renal transplantation in patients treated with tacrolimus.

Fundamental & clinical pharmacology·2004

The extra-terminal domain drives the role of BET proteins in transcription.

Nucleic acids research·2026

The Lomb-Scargle periodogram-based differentially expressed gene detection along pseudotime.

Nucleic acids research·2026

Programmed repair of disease-causing UGA premature termination codons in mammalian brain.

Nucleic acids research·2026

Effects of single and double mutations on the MYC promoter G-quadruplex using a custom G4 DNA microarray: conformational landscape and nearby guanine compensation.

Nucleic acids research·2026

Single-residue engineering of Klenow fragment enables broad acceptance of chemically modified nucleotides.

Nucleic acids research·2026

Recognition of multimolecular G-quadruplex regulates phase separation of cockayne syndrome B.

Nucleic acids research·2026

The Genetics of Coronary Artery Disease: Insights from Genome-wide Association Studies.

Current cardiology reviews·2026

Establishment of the endocrine variant extractor and its clinical application in identifying a novel GATA3 mutation in HDR syndrome.

Frontiers in endocrinology·2026

Sex- and Population-Specific Formulas for Glenoid Height-Based Assessment of Glenoid Bone Loss: A Systematic Review and Meta-analysis.

Orthopaedic journal of sports medicine·2026

Root cause discovery via permutations and Cholesky decomposition.

Journal of the Royal Statistical Society. Series B, Statistical methodology·2026

In-silico analysis of Bifidobacterium bifidum strain 900791 genome in the context of the B. bifidum pangenome.

Frontiers in cellular and infection microbiology·2026

Sex Differences in Behavioral Responses to Chronic Unpredictable Mild Stress in Swiss Mice.

The European journal of neuroscience·2026

Related Experiment Videos

Northern blot normalization with a 28S rRNA oligonucleotide probe

Related Concept Videos

Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B.

Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?

Simultaneous regression of Philadelphia chromosome and multiple nonrecurrent clonal chromosomal abnormalities with imatinib mesylate in a patient autografted 22 years before for chronic myelogenous leukemia.

GW body disassembly triggered by siRNAs independently of their silencing activity.

The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules.

Low levels of lymphocyte MDR1 gene expression during early renal transplantation in patients treated with tacrolimus.

The extra-terminal domain drives the role of BET proteins in transcription.

The Lomb-Scargle periodogram-based differentially expressed gene detection along pseudotime.

Programmed repair of disease-causing UGA premature termination codons in mammalian brain.

Effects of single and double mutations on the MYC promoter G-quadruplex using a custom G4 DNA microarray: conformational landscape and nearby guanine compensation.

Single-residue engineering of Klenow fragment enables broad acceptance of chemically modified nucleotides.

Recognition of multimolecular G-quadruplex regulates phase separation of cockayne syndrome B.

The Genetics of Coronary Artery Disease: Insights from Genome-wide Association Studies.

Establishment of the endocrine variant extractor and its clinical application in identifying a novel <i>GATA3</i> mutation in HDR syndrome.

Sex- and Population-Specific Formulas for Glenoid Height-Based Assessment of Glenoid Bone Loss: A Systematic Review and Meta-analysis.

Root cause discovery via permutations and Cholesky decomposition.

<i>In-silico</i> analysis of <i>Bifidobacterium bifidum</i> strain 900791 genome in the context of the <i>B. bifidum</i> pangenome.

Sex Differences in Behavioral Responses to Chronic Unpredictable Mild Stress in Swiss Mice.

Related Experiment Videos

Northern blot normalization with a 28S rRNA oligonucleotide probe

Related Concept Videos

Related Articles