Molecular analysis of beta-thalassemia

Significance of alpha-1-antitrypsin mRNA expression in esophageal carcinoma.

International journal of oncology·2011

Comprehensive behavioural study of GluR4 knockout mice: implication in cognitive function.

Genes, brain, and behavior·2010

Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16.

Journal of medical genetics·2007

The distribution of hereditary erythrocytic disorders associated with malaria, in a lowland area of Nepal: a micro-epidemiological study.

Annals of tropical medicine and parasitology·2007

The contactin 4 gene locus at 3p26 is a candidate gene of SCA16.

Neurology·2006

Association study of polymorphisms in the GluR5 kainate receptor gene (GRIK1) with schizophrenia.

Psychiatric genetics·2001

[Production and secretion of BSF2/IL6 in a case of hairy cell leukemia with polyclonal hypergammaglobulinemia].

Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society·1990

[Mechanism of hyperferritinemia in a case of malignant histiocytosis].

Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society·1990

[Flow cytometric analysis of immunophagocytosis using sensitized fluorescent microspheres bearing C3b].

Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society·1990

[Autoinduction of differentiation in human myelocytic leukemia cells (HL-60-Y3)].

Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society·1990

[Long-term cultures of marrow cells from the patients with aplastic anemia].

Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society·1990

[Biochemical and molecular biological studies on beta-glucuronidase in myelogenous leukemic cells].

Nihon Ketsueki Gakkai zasshi : journal of Japan Haematological Society·1990

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Molecular analysis of beta-thalassemia

Related Concept Videos

Significance of alpha-1-antitrypsin mRNA expression in esophageal carcinoma.

Comprehensive behavioural study of GluR4 knockout mice: implication in cognitive function.

Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16.

The distribution of hereditary erythrocytic disorders associated with malaria, in a lowland area of Nepal: a micro-epidemiological study.

The contactin 4 gene locus at 3p26 is a candidate gene of SCA16.

Association study of polymorphisms in the GluR5 kainate receptor gene (GRIK1) with schizophrenia.

[Production and secretion of BSF2/IL6 in a case of hairy cell leukemia with polyclonal hypergammaglobulinemia].

[Mechanism of hyperferritinemia in a case of malignant histiocytosis].

[Flow cytometric analysis of immunophagocytosis using sensitized fluorescent microspheres bearing C3b].

[Autoinduction of differentiation in human myelocytic leukemia cells (HL-60-Y3)].

[Long-term cultures of marrow cells from the patients with aplastic anemia].

[Biochemical and molecular biological studies on beta-glucuronidase in myelogenous leukemic cells].

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

Related Experiment Videos

Molecular analysis of beta-thalassemia

Related Concept Videos

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