TfM mutation and masculinization versus feminization of the mouse central nervous system

Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease.

Neurobiology of disease·1999

Genetic discrimination and screening for hemochromatosis.

Journal of public health policy·1994

[Usefulness of 99mTc-ECD SPECT in diseases of the central nerve system: special reference to a comparison with 123I-IMP and 99mTc-HM-PAO SPECT].

Kaku igaku. The Japanese journal of nuclear medicine·1992

[Surgery for the patients whose total pulmonary vascular resistance was over 700 dyne during unilateral pulmonary artery occlusion test].

[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai·1992

Myocardial oxidative metabolism in normal subjects in fasting, glucose loading and dobutamine infusion states.

Annals of nuclear medicine·1992

Glutamate and aspartate are decreased in the skin in amyotrophic lateral sclerosis.

Acta neurologica Scandinavica·1992

Virtual Cell Challenge 2026: Benchmarking zero-shot generalization across cellular contexts.

Cell·2026

Integrative spatial profiling of 3D genome organization and gene expression in tissue.

Cell·2026

DDIAS shields single-stranded DNA in mitosis and promotes vertebrate brain development.

Cell·2026

Multimodal evidence for bone lymphatics in skeletal health and repair.

Cell·2026

Lymphatic vessels invade bone in disease but are absent in health and regeneration.

Cell·2026

Modern science outreach: A guide for scientists.

Cell·2026

Identification and characterization of ethR and ethA genes impacting the sensitivity of Mycobacterium abscessus to ethionamide.

Microbiology spectrum·2026

Diagnostic accuracy of MRI and PSMA PET/CT for detection of histologically confirmed lymph node metastasis in prostate cancer: A systematic review.

Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica·2026

Racial differences in multiple myeloma survival: Associations with stem cell transplantation, insurance, and Medicaid expansion.

Cancer·2026

[Clinical manifestation and analysis of FBN1 gene variants in eight patients with Marfan syndrome].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Plasma Lactate Response to a 12-Min Walk Test Is a Poor Diagnostic Biomarker for Mitochondrial Myopathy.

JIMD reports·2026

Enrichment of CD4-CD8- cytotoxic Vδ1/3 T cells in pulmonary tuberculosis disease.

iScience·2026

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TfM mutation and masculinization versus feminization of the mouse central nervous system

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Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease.

Genetic discrimination and screening for hemochromatosis.

[Usefulness of 99mTc-ECD SPECT in diseases of the central nerve system: special reference to a comparison with 123I-IMP and 99mTc-HM-PAO SPECT].

[Surgery for the patients whose total pulmonary vascular resistance was over 700 dyne during unilateral pulmonary artery occlusion test].

Myocardial oxidative metabolism in normal subjects in fasting, glucose loading and dobutamine infusion states.

Glutamate and aspartate are decreased in the skin in amyotrophic lateral sclerosis.

Virtual Cell Challenge 2026: Benchmarking zero-shot generalization across cellular contexts.

Integrative spatial profiling of 3D genome organization and gene expression in tissue.

DDIAS shields single-stranded DNA in mitosis and promotes vertebrate brain development.

Multimodal evidence for bone lymphatics in skeletal health and repair.

Lymphatic vessels invade bone in disease but are absent in health and regeneration.

Modern science outreach: A guide for scientists.

Identification and characterization of ethR and ethA genes impacting the sensitivity of Mycobacterium abscessus to ethionamide.

Diagnostic accuracy of MRI and PSMA PET/CT for detection of histologically confirmed lymph node metastasis in prostate cancer: A systematic review.

Racial differences in multiple myeloma survival: Associations with stem cell transplantation, insurance, and Medicaid expansion.

[Clinical manifestation and analysis of FBN1 gene variants in eight patients with Marfan syndrome].

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TfM mutation and masculinization versus feminization of the mouse central nervous system

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