Letter: Satellite-stalk staining of human chromosomes

Delineation of clinical features in Wiedemann-Steiner syndrome caused by KMT2A mutations.

Clinical genetics·2015

Down-regulation of ABCC11 protein (MRP8) in human breast cancer.

Experimental oncology·2011

BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.

Oncogene·2009

A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.

Journal of dental research·2006

Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome.

Journal of clinical pathology·2006

Growth hormone therapy and scoliosis in patients with Prader-Willi syndrome.

American journal of medical genetics. Part A·2006

Safety and lipoprotein(a)-lowering effects of Kylo-11, a non-canonical, long-duration small interfering RNA targeting lipoprotein(a): a first-in-human, randomised, double-blind, placebo-controlled, phase 1 trial.

Lancet (London, England)·2026

Generalised eruptive histiocytosis mimicking lymphoma relapse in a patient with previous diffuse large B-cell lymphoma.

Lancet (London, England)·2026

Physiotherapist-led care for musculoskeletal conditions in the emergency department (RESHAP-ED): a randomised controlled trial with economic evaluation.

Lancet (London, England)·2026

Systematic reviews and the needs of the adolescent transgender health care field.

Lancet (London, England)·2026

Pre-eclampsia.

Lancet (London, England)·2026

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Frontiers in cell and developmental biology·2026

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

Planta·2026

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

The FEBS journal·2026

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Stem cell reports·2026

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo·2026

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Medicina (Kaunas, Lithuania)·2026

Related Experiment Videos

Letter: Satellite-stalk staining of human chromosomes

Related Concept Videos

Delineation of clinical features in Wiedemann-Steiner syndrome caused by KMT2A mutations.

Down-regulation of ABCC11 protein (MRP8) in human breast cancer.

BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.

A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.

Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome.

Growth hormone therapy and scoliosis in patients with Prader-Willi syndrome.

Safety and lipoprotein(a)-lowering effects of Kylo-11, a non-canonical, long-duration small interfering RNA targeting lipoprotein(a): a first-in-human, randomised, double-blind, placebo-controlled, phase 1 trial.

Generalised eruptive histiocytosis mimicking lymphoma relapse in a patient with previous diffuse large B-cell lymphoma.

Physiotherapist-led care for musculoskeletal conditions in the emergency department (RESHAP-ED): a randomised controlled trial with economic evaluation.

Systematic reviews and the needs of the adolescent transgender health care field.

Pre-eclampsia.

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Related Experiment Videos

Letter: Satellite-stalk staining of human chromosomes

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