So many needles, so much hay

Same author

A novel somatostatin-immunoreactive mossy fiber pathway associated with HSP25-immunoreactive purkinje cell stripes in the mouse cerebellum.

The Journal of comparative neurology·2009

Same author

Identifying transcribed sequences in arrayed bacteriophage or cosmid libraries.

Current protocols in human genetics·2008

Same author

Null mutant mouse models of somatostatin and cortistatin, and their receptors.

Molecular and cellular endocrinology·2008

Same author

Proopiomelanocortin heterozygous and homozygous null mutant mice develop pituitary adenomas.

Cellular and molecular biology (Noisy-le-Grand, France)·2006

Same author

Adrenocorticotropic hormone directly stimulates testosterone production by the fetal and neonatal mouse testis.

Endocrinology·2003

Same author

Increased HTLV-I proviral load and preferential expansion of HTLV-I Tax-specific CD8+ T cells in cerebrospinal fluid from patients with HAM/TSP.

Annals of neurology·2002

Same journal

Circulating MYOM3 fragments reflect disease severity and therapeutic efficacy in tubular aggregate myopathy and Stormorken syndrome.

Human molecular genetics·2026

Same journal

The FVB-nmd SMARD1 mouse presents with early respiratory deficits and pathology that significantly impact lifespan.

Human molecular genetics·2026

Same journal

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

Human molecular genetics·2026

Same journal

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Human molecular genetics·2026

Same journal

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Human molecular genetics·2026

Same journal

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Human molecular genetics·2026

Related Experiment Videos

So many needles, so much hay

Related Concept Videos

A novel somatostatin-immunoreactive mossy fiber pathway associated with HSP25-immunoreactive purkinje cell stripes in the mouse cerebellum.

Identifying transcribed sequences in arrayed bacteriophage or cosmid libraries.

Null mutant mouse models of somatostatin and cortistatin, and their receptors.

Proopiomelanocortin heterozygous and homozygous null mutant mice develop pituitary adenomas.

Adrenocorticotropic hormone directly stimulates testosterone production by the fetal and neonatal mouse testis.

Increased HTLV-I proviral load and preferential expansion of HTLV-I Tax-specific CD8+ T cells in cerebrospinal fluid from patients with HAM/TSP.

Circulating MYOM3 fragments reflect disease severity and therapeutic efficacy in tubular aggregate myopathy and Stormorken syndrome.

The FVB-nmd SMARD1 mouse presents with early respiratory deficits and pathology that significantly impact lifespan.

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Related Experiment Videos

So many needles, so much hay

Related Concept Videos

Related Articles

A novel somatostatin-immunoreactive mossy fiber pathway associated with HSP25-immunoreactive purkinje cell stripes in the mouse cerebellum.

Identifying transcribed sequences in arrayed bacteriophage or cosmid libraries.

Null mutant mouse models of somatostatin and cortistatin, and their receptors.

Proopiomelanocortin heterozygous and homozygous null mutant mice develop pituitary adenomas.

Adrenocorticotropic hormone directly stimulates testosterone production by the fetal and neonatal mouse testis.

Increased HTLV-I proviral load and preferential expansion of HTLV-I Tax-specific CD8+ T cells in cerebrospinal fluid from patients with HAM/TSP.

Circulating MYOM3 fragments reflect disease severity and therapeutic efficacy in tubular aggregate myopathy and Stormorken syndrome.

The FVB-nmd SMARD1 mouse presents with early respiratory deficits and pathology that significantly impact lifespan.

Utrophin requires α-Syntrophin to maintain neuromuscular junction integrity in mdx mice.

A novel gene ACTRT3 mutations induce sperm malformations and fertilization failure via Acrosomal ultrastructural defects.

Nucleic acid-based therapeutic strategies for modulator-refractory cystic fibrosis-causing variants.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.