Two unusual G-band variants of the short arm of chromosome 9

Effect of age in rodent models of focal and forebrain ischemia.

Stroke·1996

bcl-w, a novel member of the bcl-2 family, promotes cell survival.

Oncogene·1996

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene.

Genomics·1996

The effects of calcium on the thermal stability and activity of manganese peroxidase.

Archives of biochemistry and biophysics·1996

Asymptomatic large pituitary adenomas discovered at autopsy.

Surgical neurology·1996

Characterization and chromosomal localization of the human A2a adenosine receptor gene: ADORA2A.

Biochemical and biophysical research communications·1996

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

A Homozygous ALCAM-CBLB Deletion at 3q13.11-q13.12 Defines a Candidate Novel Oculo-Skeletal-Immune Contiguous Gene Deletion Syndrome.

Clinical genetics·2026

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

Clinical genetics·2026

Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

Clinical genetics·2026

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Clinical genetics·2026

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

Clinical genetics·2026

Non-linear Age-related Patterns of Sleep Architecture in First-episode Schizophrenia: A Restricted Cubic Spline Analysis.

Current neuropharmacology·2026

Non-redundant functions of insulin/FOXO and EcR signaling pathways regulate accessory gland structure, function and male fertility in Drosophila.

Journal of insect physiology·2026

SLC32A1 regulates puberty onset in female mice by modulating GnRH neuron function through Kisspeptin and GABA-GABAB receptor signaling.

Theriogenology·2026

Genetic Causes of Disorders of Sex Development in Thai Children.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation·2026

A novel microdeletion syndrome involving 17q23.3 region in a child with short stature and multiple congenital anomalies: A Case Report.

Cytogenetic and genome research·2026

BdPiwi is essential for gametogenesis and post-embryonic development in the oriental fruit fly, Bactrocera dorsalis.

Pest management science·2026

Related Experiment Videos

Two unusual G-band variants of the short arm of chromosome 9

Related Concept Videos

Effect of age in rodent models of focal and forebrain ischemia.

bcl-w, a novel member of the bcl-2 family, promotes cell survival.

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase gene.

The effects of calcium on the thermal stability and activity of manganese peroxidase.

Asymptomatic large pituitary adenomas discovered at autopsy.

Characterization and chromosomal localization of the human A2a adenosine receptor gene: ADORA2A.

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

A Homozygous ALCAM-CBLB Deletion at 3q13.11-q13.12 Defines a Candidate Novel Oculo-Skeletal-Immune Contiguous Gene Deletion Syndrome.

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

Non-linear Age-related Patterns of Sleep Architecture in First-episode Schizophrenia: A Restricted Cubic Spline Analysis.

Non-redundant functions of insulin/FOXO and EcR signaling pathways regulate accessory gland structure, function and male fertility in Drosophila.

SLC32A1 regulates puberty onset in female mice by modulating GnRH neuron function through Kisspeptin and GABA-GABAB receptor signaling.

Genetic Causes of Disorders of Sex Development in Thai Children.

A novel microdeletion syndrome involving 17q23.3 region in a child with short stature and multiple congenital anomalies: A Case Report.

BdPiwi is essential for gametogenesis and post-embryonic development in the oriental fruit fly, Bactrocera dorsalis.

Related Experiment Videos

Two unusual G-band variants of the short arm of chromosome 9

Related Concept Videos

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