The fluorescence pattern of the human karyotype

Spectroscopic identification of r-process nucleosynthesis in a double neutron-star merger.

Nature·2017

Solvent control of intramolecular proton transfer: is 4-hydroxy-3-(piperidin-1-ylmethyl)-1-naphthaldehyde a proton crane?

Physical chemistry chemical physics : PCCP·2017

4-Hydroxy-1-naphthaldehydes: proton transfer or deprotonation.

Physical chemistry chemical physics : PCCP·2015

GRB 130427A: a nearby ordinary monster.

Science (New York, N.Y.)·2013

An optical supernova associated with the X-ray flash XRF 060218.

Nature·2006

A photometric redshift of z = 6.39 +/- 0.12 for GRB 050904.

Nature·2006

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

Hereditas·2026

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

Hereditas·2026

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Hereditas·2026

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

Hereditas·2026

miR-146b-5p serves as a novel biomarker for acute myocardial infarction and is involved in regulating oxidized low-density lipoprotein-induced endothelial injury through targeting PRKAR2A.

Hereditas·2026

Whole blood miRNA expression signatures as predictors of neoadjuvant chemotherapy response in triple-negative breast cancer.

Hereditas·2026

MAGIC populations: a next-generation framework for dissecting complex quantitative traits and accelerating molecular breeding in crops.

Frontiers in plant science·2026

Genome evolution and long-term demographic history in true crocodiles.

G3 (Bethesda, Md.)·2026

Cytoplasmic RBM20 granules modulate non-RBM20 target splicing through interactions with other splicing factors.

Nucleic acids research·2026

A Homozygous NUP210L Variant Is Associated With Severe Defects in Human Spermiogenesis.

Andrology·2026

Embryogenesis: Centering and decentering during cleavage.

Current biology : CB·2026

Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease.

Research square·2026

Related Experiment Videos

The fluorescence pattern of the human karyotype

Related Concept Videos

Spectroscopic identification of r-process nucleosynthesis in a double neutron-star merger.

Solvent control of intramolecular proton transfer: is 4-hydroxy-3-(piperidin-1-ylmethyl)-1-naphthaldehyde a proton crane?

4-Hydroxy-1-naphthaldehydes: proton transfer or deprotonation.

GRB 130427A: a nearby ordinary monster.

An optical supernova associated with the X-ray flash XRF 060218.

A photometric redshift of z = 6.39 +/- 0.12 for GRB 050904.

SNP rs7430456 mediated LINC00578 drives triple negative breast cancer through regulating miR-143-5p expression.

BFLF1 gene polymorphisms are associated with increased mortality in patients with EBV-associated diseases.

miR-1-3p, as a novel diagnostic and prognostic biomarker, aggravates pancreatic acinar cell injury in acute pancreatitis by targeting GNPTAB.

Identification of FOXK1 and SEMA7A as key genes associated with m6A-related programmed cell death in diabetic retinopathy.

miR-146b-5p serves as a novel biomarker for acute myocardial infarction and is involved in regulating oxidized low-density lipoprotein-induced endothelial injury through targeting PRKAR2A.

Whole blood miRNA expression signatures as predictors of neoadjuvant chemotherapy response in triple-negative breast cancer.

MAGIC populations: a next-generation framework for dissecting complex quantitative traits and accelerating molecular breeding in crops.

Genome evolution and long-term demographic history in true crocodiles.

Cytoplasmic RBM20 granules modulate non-RBM20 target splicing through interactions with other splicing factors.

A Homozygous NUP210L Variant Is Associated With Severe Defects in Human Spermiogenesis.

Embryogenesis: Centering and decentering during cleavage.

Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease.

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The fluorescence pattern of the human karyotype

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