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Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency

Molecular psychiatry, 2012-04, Vol.17 (4), p.451-466

2012

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Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors

Development (Cambridge), 1998-01, Vol.125 (1), p.85-94

1998

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Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

Human molecular genetics, 2001, Vol.10 (1), p.39-45

2001

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Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

Journal of medical genetics, 2004-09, Vol.41 (9), p.669-678

2004

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GDNF Is a Chemoattractant for Enteric Neural Cells

Developmental biology, 2001-01, Vol.229 (2), p.503-516

2001

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Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression

Developmental biology, 2004-01, Vol.265 (2), p.329-340

2004

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Identification and enrichment of colony-forming cells from the adult murine pituitary

Experimental cell research, 2005-08, Vol.308 (1), p.166-176

2005

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SOX3 is required during the formation of the hypothalamo-pituitary axis

Nature genetics, 2004-03, Vol.36 (3), p.247-255

2004

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Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Nature genetics, 1998-06, Vol.19 (2), p.125-133

1998

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HESX1: a novel gene implicated in a familial form of septo-optic dysplasia

Acta Paediatrica, 1999-12, Vol.88 (s433), p.49-54

1999

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Increased Gene Dosage at Xq26–q27 Is Associated with X-Linked Hypopituitarism

Genomics (San Diego, Calif.), 2002-04, Vol.79 (4), p.553-559

2002

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An anterior signalling centre in Xenopus revealed by the homeobox gene XHex

Current biology, 1999-09, Vol.9 (17), p.946,S1-954,S1

1999

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

American journal of human genetics, 2012-01, Vol.90 (1), p.152-160

2012

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Sequence, Genomic Organization, and Expression of the Novel Homeobox Gene Hesx1

The Journal of biological chemistry, 1995-02, Vol.270 (8), p.3869-3875

1995

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HES-1, a novel homeobox gene expressed by murine embryonic stem cells, identifies a new class of homeobox genes

Nucleic acids research, 1992-11, Vol.20 (21), p.5840-5840

1992

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Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties

Open biology, 2024-04, Vol.14 (4), p.230383-13

2024

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Developmentally regulated expression of the regulator of G-protein signaling gene 2 ( Rgs2) in the embryonic mouse pituitary

Gene Expression Patterns, 2005-02, Vol.5 (3), p.305-311

2005

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Hesx1, a Homeobox Gene Expressed by Murine Embryonic Stem Cells, Maps to Mouse Chromosome 14, Bands A3-B

Genomics (San Diego, Calif.), 1993-11, Vol.18 (2), p.464-466

1993

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Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

American journal of human genetics, 2005-05, Vol.76 (5), p.833-849

2005

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Adrenocorticotropin Deficiency in Combined Pituitary Hormone Deficiency Patients Homozygous for a Novel PROP1 Deletion

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4556-4561

2000

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Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3[zeta] deficiency

Molecular psychiatry, 2012-04, Vol.17 (4), p.451

2012

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Molecular genetics of septo-optic dysplasia

Hormone research, 2000-01, Vol.53 Suppl 1, p.26-33

2000

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Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

Journal of medical genetics, 2007-04, Vol.44 (4), p.e75-e75

2007

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Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)

Clinical endocrinology (Oxford), 2005-07, Vol.63 (1), p.10-18

2005

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Recent Judicial Developments of Interest to Oil and Gas Lawyers

Alberta law review, 2015-12, p.233

2015

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Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency

Hex: a homeobox gene revealing peri-implantation asymmetry in the mouse embryo and an early transient marker of endothelial cell precursors

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

GDNF Is a Chemoattractant for Enteric Neural Cells

Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression

Identification and enrichment of colony-forming cells from the adult murine pituitary

SOX3 is required during the formation of the hypothalamo-pituitary axis

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

HESX1: a novel gene implicated in a familial form of septo-optic dysplasia

Increased Gene Dosage at Xq26–q27 Is Associated with X-Linked Hypopituitarism

An anterior signalling centre in Xenopus revealed by the homeobox gene XHex

PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Sequence, Genomic Organization, and Expression of the Novel Homeobox Gene Hesx1

HES-1, a novel homeobox gene expressed by murine embryonic stem cells, identifies a new class of homeobox genes

Mapping combinatorial expression of non-clustered protocadherins in the developing brain identifies novel PCDH19-mediated cell adhesion properties

Developmentally regulated expression of the regulator of G-protein signaling gene 2 ( Rgs2) in the embryonic mouse pituitary

Hesx1, a Homeobox Gene Expressed by Murine Embryonic Stem Cells, Maps to Mouse Chromosome 14, Bands A3-B

Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

Adrenocorticotropin Deficiency in Combined Pituitary Hormone Deficiency Patients Homozygous for a Novel PROP1 Deletion

Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3[zeta] deficiency

Molecular genetics of septo-optic dysplasia

Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)

Recent Judicial Developments of Interest to Oil and Gas Lawyers

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