Liver-specific enzymes in human fibroblast x rat hepatoma somatic cell hybrids

Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.

Journal of community genetics·2018

Recommendations for locus-specific databases and their curation.

Human mutation·2007

DNA sequence and analysis of human chromosome 9.

Nature·2004

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

Human molecular genetics·2001

Type VIII collagen: heterotrimeric chain association.

The international journal of biochemistry & cell biology·2001

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma.

American journal of human genetics·2000

Plant genetic resources: prediction by isozyme markers and ecology.

Isozymes·1987

Human aldehyde dehydrogenase isozymes and alcohol sensitivity.

Isozymes·1987

Sensitive techniques for the detection of genetic variation in human isozymes.

Isozymes·1987

Baboon alcohol dehydrogenase isozymes: phenotypic changes in liver following chronic consumption of alcohol.

Isozymes·1987

Human arginase isozymes.

Isozymes·1987

An Open-Label, Dose-Escalation Trial of Psilocybin-Assisted Therapy for Bipolar II Depression.

The Journal of clinical psychiatry·2026

Analysis of Complications Associated with Basivertebral Nerve Ablation for Vertebrogenic Low Back Pain: A Multicenter Retrospective Cohort Study of 1,145 Patients.

Pain medicine (Malden, Mass.)·2026

Fibroblast-Derived LIF Suppresses Osteogenesis Through LIFR/ STAT3 Signalling in Fracture Nonunion.

Current medicinal chemistry·2026

Persistent chylothorax despite complete thoracic duct ligation: lymphangiographic findings and outcomes of thoracic duct embolization.

Journal of vascular and interventional radiology : JVIR·2026

Chronic Contractile Activity Remediates Lysosomal Dysfunction in a Muscle Cell Lysosomal Disease Model.

Journal of cellular physiology·2026

Comprehensive Isolation Strategy for Intestinal Epithelial and Fibroblast Cells from Healthy and Tumor Human Tissues.

Methods in molecular biology (Clifton, N.J.)·2026

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Liver-specific enzymes in human fibroblast x rat hepatoma somatic cell hybrids

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Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.

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DNA sequence and analysis of human chromosome 9.

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

Type VIII collagen: heterotrimeric chain association.

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma.

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Sensitive techniques for the detection of genetic variation in human isozymes.

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Liver-specific enzymes in human fibroblast x rat hepatoma somatic cell hybrids

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