The molecular genetics of differentiation

SAMA's principled positioning in upholding global medical ethics.

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde·2026

Rethinking interleukin-6 blockade for treatment of COVID-19.

Medical hypotheses·2020

Rapid reperitonealization and wound healing in a preclinical model of abdominal trauma repair with a composite mesh.

International journal of surgery (London, England)·2015

Higher capecitabine AUC in elderly patients with advanced colorectal cancer (SWOGS0030).

British journal of cancer·2013

Treatment of sound errors in aphasia and apraxia of speech: Effects of phonological complexity.

Aphasiology·2012

Complex evolution of a highly conserved microsatellite locus in several fish species.

Journal of fish biology·2010

The Drosophila SWI/SNF complex sub-unit Bap60 is required for training-induced gene transcription during long-term memory formation.

Genetics·2026

A genetic model of copulatory wounding in Drosophila melanogaster.

Genetics·2026

Uncertainty-aware breeding decisions: MCMC-based optimum contribution selection increases breeding decision robustness.

Genetics·2026

The evolution of genetic drift over 50,000 generations.

Genetics·2026

Ribosome-associated chaperones integrate co-translational mitochondrial protein import, stress signaling and proteostasis in Saccharomyces cerevisiae.

Genetics·2026

Identification of a "new" crystal/Su(Ste) locus on the Drosophila melanogaster Y chromosome, resembling a piRNA cluster regulating Stellate repeats and transposons.

Genetics·2026

Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.

Acta crystallographica. Section F, Structural biology communications·2026

Recurrent episodes of hypoglycemia as an initial presentation of pituitary stalk interruption syndrome: A case report.

Radiology case reports·2026

EXTL3 dysfunction identified as a driver of aberrant bone development in severe familial ankylosing spondylitis.

Annals of the rheumatic diseases·2026

Dopamine Receptor D2 gene Polymorphisms rs2005313, rs4274224, and rs4938019 in Pakistani Patients with Schizophrenia:a Diagnostic Tool for Schizophrenia.

Journal of molecular neuroscience : MN·2026

Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.

Clinical endocrinology·2026

CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.

European journal of endocrinology·2026

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The molecular genetics of differentiation

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SAMA's principled positioning in upholding global medical ethics.

Rethinking interleukin-6 blockade for treatment of COVID-19.

Rapid reperitonealization and wound healing in a preclinical model of abdominal trauma repair with a composite mesh.

Higher capecitabine AUC in elderly patients with advanced colorectal cancer (SWOGS0030).

Treatment of sound errors in aphasia and apraxia of speech: Effects of phonological complexity.

Complex evolution of a highly conserved microsatellite locus in several fish species.

The Drosophila SWI/SNF complex sub-unit Bap60 is required for training-induced gene transcription during long-term memory formation.

A genetic model of copulatory wounding in Drosophila melanogaster.

Uncertainty-aware breeding decisions: MCMC-based optimum contribution selection increases breeding decision robustness.

The evolution of genetic drift over 50,000 generations.

Ribosome-associated chaperones integrate co-translational mitochondrial protein import, stress signaling and proteostasis in Saccharomyces cerevisiae.

Identification of a "new" crystal/Su(Ste) locus on the Drosophila melanogaster Y chromosome, resembling a piRNA cluster regulating Stellate repeats and transposons.

Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.

Recurrent episodes of hypoglycemia as an initial presentation of pituitary stalk interruption syndrome: A case report.

EXTL3 dysfunction identified as a driver of aberrant bone development in severe familial ankylosing spondylitis.

Dopamine Receptor D2 gene Polymorphisms rs2005313, rs4274224, and rs4938019 in Pakistani Patients with Schizophrenia:a Diagnostic Tool for Schizophrenia.

Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.

CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.

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The molecular genetics of differentiation

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