[What is the use of cryopreserved tissue and cell banks? A geneticist's view point]

A retinoid acid 'resistant' t(15;17) acute promyelocytic leukemia cell line: isolation, morphological, immunological, and molecular features.

Leukemia·1992

Relapse as acute monoblastic leukemia (AML-M5) of t(6;9) acute myeloblastic leukemia (AML-M2).

Leukemia·1992

A new gene, BCM, on chromosome 16 is fused to the interleukin 2 gene by a t(4;16)(q26;p13) translocation in a malignant T cell lymphoma.

The EMBO journal·1992

Tumor-associated karyotypic lesions coselected with in vitro macrophage differentiation.

Genes, chromosomes & cancer·1992

Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia.

Cancer genetics and cytogenetics·1992

A third tal-1 promoter is specifically used in human T cell leukemias.

The Journal of experimental medicine·1992

[Case #4: Bronchiolar adenoma].

Annales de pathologie·2026

[Imaging of pulmonary nodules: A diagnostic approach].

Annales de pathologie·2026

[Case 3. Sclerosing pneumocytoma: A diagnostic pitfall mimicking pulmonary adenocarcinoma].

Annales de pathologie·2026

[New developments in grading of astrocytomas, IDH-mutant: Study of the impact of update 12 of cIMPACT-NOW].

Annales de pathologie·2026

[Exogenous ochronosis: An underdiagnosed cause of acquired facial hyperpigmentation].

Annales de pathologie·2026

[Diagnostic approach to non-cutaneous T-cell lymphomas in 2025: What pitfalls and how should they be classified?]

Annales de pathologie·2026

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Diagnostics (Basel, Switzerland)·2026

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Drug delivery·2026

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

Frontiers in plant science·2026

Rapid and Sensitive Detection of USP26 Cluster Variants Based on CRISPR/Cas12a.

Human mutation·2026

Integrative long-read sequencing, RNA-seq and machine learning framework characterizes and predicts autosomal silencing in unbalanced X-autosome translocations.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Large intra-chromosome heterogeneity leads to emergent nonlinear mechanics.

Nature physics·2026

Related Experiment Videos

[What is the use of cryopreserved tissue and cell banks? A geneticist's view point]

Related Concept Videos

A retinoid acid 'resistant' t(15;17) acute promyelocytic leukemia cell line: isolation, morphological, immunological, and molecular features.

Relapse as acute monoblastic leukemia (AML-M5) of t(6;9) acute myeloblastic leukemia (AML-M2).

A new gene, BCM, on chromosome 16 is fused to the interleukin 2 gene by a t(4;16)(q26;p13) translocation in a malignant T cell lymphoma.

Tumor-associated karyotypic lesions coselected with in vitro macrophage differentiation.

Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia.

A third tal-1 promoter is specifically used in human T cell leukemias.

[Case #4: Bronchiolar adenoma].

[Imaging of pulmonary nodules: A diagnostic approach].

[Case 3. Sclerosing pneumocytoma: A diagnostic pitfall mimicking pulmonary adenocarcinoma].

[New developments in grading of astrocytomas, IDH-mutant: Study of the impact of update 12 of cIMPACT-NOW].

[Exogenous ochronosis: An underdiagnosed cause of acquired facial hyperpigmentation].

[Diagnostic approach to non-cutaneous T-cell lymphomas in 2025: What pitfalls and how should they be classified?]

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

Rapid and Sensitive Detection of USP26 Cluster Variants Based on CRISPR/Cas12a.

Integrative long-read sequencing, RNA-seq and machine learning framework characterizes and predicts autosomal silencing in unbalanced X-autosome translocations.

Large intra-chromosome heterogeneity leads to emergent nonlinear mechanics.

Related Experiment Videos

[What is the use of cryopreserved tissue and cell banks? A geneticist's view point]

Related Concept Videos

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