Another example of the beta-thalassemia mutation, IVS-I (-2) or codon 30 (A-->G), found in a Chinese family

[Establishment and validation of prognosis predictive model using m6A RNA methylation regulators in children acute myeloid leukemia].

Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]·2021

Current status of thalassemia in minority populations in Guangxi, China.

Clinical genetics·2007

[Antimutagenic substances in the Armeniacae semen and Persicae semen].

Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan·1992

Investigation of peroxisomal lipid beta-oxidation enzymes in guinea pig liver peroxisomes by immunoblotting and immunocytochemistry.

The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society·1992

Phenotypic and genotypic characterization of 14 leukemia and lymphoma cell lines with 11q23 translocations.

Leukemia research·1992

Fire death and hypoxic death.

Nihon hoigaku zasshi = The Japanese journal of legal medicine·1992

Precision Medicine in Sickle Cell Disease: From Molecular Pathways to Curative Strategies.

Hemoglobin·2026

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Hemoglobin·2026

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Hemoglobin·2026

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Hemoglobin·2026

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Hemoglobin·2026

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Hemoglobin·2026

Sequence diversity and forensic efficiency of Y-STRs in the Han population of Yunnan Province, Southwest China.

International journal of legal medicine·2026

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

American journal of medical genetics. Part A·2026

Repeat-length variation generates stable TTGGG-family G-quadruplex motifs in plant mitochondrial genomes.

Planta·2026

A KIAA0586 c.1815G>A Founder Allele Associated with Short-Rib Polydactyly Syndrome Type IV in Romani Families.

medRxiv : the preprint server for health sciences·2026

A Microfluidics-Based Assay for the Discovery of Gametogenic Rejuvenation Factors in Saccharomyces cerevisiae.

Journal of visualized experiments : JoVE·2026

Beyond two alleles: multiallelic genotypic selection and its estimation from time-series data.

BMC genomics·2026

Related Experiment Videos

Another example of the beta-thalassemia mutation, IVS-I (-2) or codon 30 (A-->G), found in a Chinese family

Related Concept Videos

[Establishment and validation of prognosis predictive model using m6A RNA methylation regulators in children acute myeloid leukemia].

Current status of thalassemia in minority populations in Guangxi, China.

[Antimutagenic substances in the Armeniacae semen and Persicae semen].

Investigation of peroxisomal lipid beta-oxidation enzymes in guinea pig liver peroxisomes by immunoblotting and immunocytochemistry.

Phenotypic and genotypic characterization of 14 leukemia and lymphoma cell lines with 11q23 translocations.

Fire death and hypoxic death.

Precision Medicine in Sickle Cell Disease: From Molecular Pathways to Curative Strategies.

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Sequence diversity and forensic efficiency of Y-STRs in the Han population of Yunnan Province, Southwest China.

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

Repeat-length variation generates stable TTGGG-family G-quadruplex motifs in plant mitochondrial genomes.

A KIAA0586 c.1815G>A Founder Allele Associated with Short-Rib Polydactyly Syndrome Type IV in Romani Families.

A Microfluidics-Based Assay for the Discovery of Gametogenic Rejuvenation Factors in Saccharomyces cerevisiae.

Beyond two alleles: multiallelic genotypic selection and its estimation from time-series data.

Related Experiment Videos

Another example of the beta-thalassemia mutation, IVS-I (-2) or codon 30 (A-->G), found in a Chinese family

Related Concept Videos

Related Articles