Sage Journals: Discover world-class research

Open access

Research article

First published 2007-1

Beyond Westermarck: Can Shared Mothering or Maternal Phenotype Matching Account for Incest Avoidance?

David Livingstone Smith

Evolutionary Psychology

Free access

Research article

First published 2012

Electrical stimulation directs engineered cardiac tissue to an age-matched native phenotype

Richard A Lasher, Aric Q Pahnke, Jeffrey M Johnson [...]

Journal of Tissue Engineering

Retricted access

Research article

First published 2010-12

Out of Sight,Out of Mind: Family Resemblances in Lesbian Donor Conception

Petra Nordqvist

Sociology

Retricted access

Research article

First published

Pathway Analysis of Microarray Data via Regression

A.J. Adewale, I. Dinu, J.D. Potter [...]

Journal of Computational Biology

Retricted access

Research article

First published 2002-1

Construction and Characterization of a Full-Length HIV-1 92UG001 Subtype D Infectious Molecular Clone

P. Novelli, C. Vella, J. Oxford [...]

AIDS Research and Human Retroviruses

Retricted access

Research article

First published 2015-2

Trust in standards: Transitioning clinical exome sequencing from bench to bedside

Stefan Timmermans

Social Studies of Science

Free access

Research article

First published 2006-10

Genotype and Phenotype Relationship in MLS B Resistance in Streptococcus Pyogenes and Streptococcus Agalactiae Isolated in Central Italy

I. Santino, F. Scazzocchio, F. Berlutti [...]

International Journal of Immunopathology and Pharmacology

Free access

Research article

First published 2004-1

Validation: The New Challenge for Pathology

Robert D. Cardiff, Andrea Rosner, Michael A. Hogarth [...]

Toxicologic Pathology

Retricted access

Research article

First published 2014-09

Monocytes from Metabolic Syndrome Subjects Exhibit a Proinflammatory M1 Phenotype

Xinpu Chen, Sridevi Devaraj

Metabolic Syndrome and Related Disorders

Retricted access

Case report

First published 2023-3

Severe Ciliopathy-Like Phenotype in an Infant With a Novel MPDU1 Missense Variant

Sihem Darouich, Houda Bellamine, Ichrak Khamassi

Pediatric and Developmental Pathology

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