The glial cells in the reptilian brain and spinal cord; Golgi study

Disruption of neuronal migration in the neocortex of the dreher mutant mouse.

Brain research. Developmental brain research·1994

Abnormal distribution of acetylcholinesterase activity in the hippocampal formation of the dreher mutant mouse.

Brain research·1993

Thermoluminescence and flash-induced oxygen yield in herbicide resistant mutants of the D1 protein in Synechococcus PCC7942.

Biochimica et biophysica acta·1992

Fish egg glycophosphoproteins have species-specific N-linked glycan units previously found in a storage pool of free glycan chains.

The Journal of biological chemistry·1992

Neutralizing activity of human antibodies against the structural protein of human T-cell lymphotropic virus type I.

International journal of cancer·1992

Two types of septic shock classified by the plasma levels of cytokines and endotoxin.

Circulatory shock·1992

Spatio-temporal distribution of eosinophils in the mouse uterus during peri-implantation period.

Okajimas folia anatomica Japonica·2020

Editorial: Suspension notice.

Okajimas folia anatomica Japonica·2020

Factors influencing dental arch form.

Okajimas folia anatomica Japonica·2019

Morphology of the lingual papillae of the bharal (Pseudois nayaur).

Okajimas folia anatomica Japonica·2019

Morphology of the Lingual Papillae of the Japanese lesser flying squirrel and four-toed hedgehog.

Okajimas folia anatomica Japonica·2019

A novel device to prevent osteoporosis by promoting bone metabolism using a newly developed double-loading stimulation with vibration and shaking.

Okajimas folia anatomica Japonica·2019

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

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The glial cells in the reptilian brain and spinal cord; Golgi study

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Disruption of neuronal migration in the neocortex of the dreher mutant mouse.

Abnormal distribution of acetylcholinesterase activity in the hippocampal formation of the dreher mutant mouse.

Thermoluminescence and flash-induced oxygen yield in herbicide resistant mutants of the D1 protein in Synechococcus PCC7942.

Fish egg glycophosphoproteins have species-specific N-linked glycan units previously found in a storage pool of free glycan chains.

Neutralizing activity of human antibodies against the structural protein of human T-cell lymphotropic virus type I.

Two types of septic shock classified by the plasma levels of cytokines and endotoxin.

Spatio-temporal distribution of eosinophils in the mouse uterus during peri-implantation period.

Editorial: Suspension notice.

Factors influencing dental arch form.

Morphology of the lingual papillae of the bharal (Pseudois nayaur).

Morphology of the Lingual Papillae of the Japanese lesser flying squirrel and four-toed hedgehog.

A novel device to prevent osteoporosis by promoting bone metabolism using a newly developed double-loading stimulation with vibration and shaking.

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

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Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

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