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Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells

Clinical epigenetics, 2022-12, Vol.14 (1), p.190-190, Article 190

2022

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Syndromic Short Stature in Patients with a Germline Mutation in the LIM Homeobox LHX4

American journal of human genetics, 2001-11, Vol.69 (5), p.961-968

2001

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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

Nature genetics, 2000-06, Vol.25 (2), p.182-186

2000

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Alternatively Spliced Forms in the Cytoplasmic Domain of the Human Growth Hormone (GH) Receptor Regulate Its Ability to Generate a Soluble GH-Binding Protein

Proceedings of the National Academy of Sciences - PNAS, 1996-10, Vol.93 (20), p.10723-10728

1996

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Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development

Gene Expression Patterns, 2004-12, Vol.5 (2), p.279-284

2004

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Pituitary stalk interruption syndrome : A clinical-biological-genetic assessment of its pathogenesis

The journal of clinical endocrinology and metabolism, 1997-10, Vol.82 (10), p.3450-3454

1997

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Nine novel growth hormone receptor gene mutations in patients with Laron syndrome

The journal of clinical endocrinology and metabolism, 1997-02, Vol.82 (2), p.435-437

1997

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A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH‐binding activity by abolishing receptor homodimerization

The EMBO journal, 1994-03, Vol.13 (6), p.1386-1395

1994

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Spectrum of growth hormone receptor mutations and associated haplotypes in Laron syndrome

Human molecular genetics, 1993-04, Vol.2 (4), p.355-359

1993

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Expression and binding properties of two isoforms of the human growth hormone receptor

FEBS letters, 1993-03, Vol.319 (1), p.16-20

1993

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Defective Membrane Expression of Human Growth Hormone (GH) Receptor Causes Laron-Type GH Insensitivity Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1991-11, Vol.88 (22), p.10272-10276

1991

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A naturally occurring growth hormone receptor mutation : in vivo and in vitro evidence for the functional importance of the WS motif common to all members of the cytokine receptor superfamily

Molecular endocrinology (Baltimore, Md.), 1993-06, Vol.7 (6), p.806-814

1993

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Recurrent nonsense mutations in the growth hormone receptor from patients with Laron Dwarfism

The Journal of clinical investigation, 1991-03, Vol.87 (3), p.1098-1102

1991

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Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalities

European journal of endocrinology, 2012-07, Vol.167 (1), p.85-91

2012

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Purification of RNA-free plasmid DNA using alkaline extraction followed by ultrogel A2 column chromatography

Analytical biochemistry, 1985-01, Vol.148 (1), p.121-126

1985

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Molecular study of the retrovirus-like transposable element 412, a 20-OH ecdysone responsive repetitive sequence in Drosophila cultured cells

Nucleic acids research, 1988-01, Vol.16 (2), p.455-470

1988

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20-Hydroxyecdysone regulates cytoplasmic actin gene expression in Drosophila cultured cells

Nucleic acids research, 1987-03, Vol.15 (6), p.2549-2561

1987

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20-OH-ecdysone regulates 60 C β tubulin gene expression in Kc cells and during Drosophila development

Experimental cell research, 1989-09, Vol.184 (1), p.241-249

1989

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Evolutionary divergence of the truncated growth hormone receptor isoform in its ability to generate a soluble growth hormone binding protein

Molecular and cellular endocrinology, 1998-02, Vol.137 (1), p.79-84

1998

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Pathologie moléculaire des facteurs de transcription impliqués dans le développement de l'antéhypophyse

Archives de pédiatrie (Paris), 2000-05, Vol.7, p.218s-220s

2000

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Species-specific Alternative Splice Mimicry at the Growth Hormone Receptor Locus Revealed by the Lineage of Retroelements during Primate Evolution. A novel mechanism accounting for protein diversity between and within species

The Journal of biological chemistry, 2000-06, Vol.275 (25), p.18664-18669

2000

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Expression of a new β tubulin subunit is induced by 20-hydroxyecdysone in drosophila cultured cells

Biochemical and biophysical research communications, 1986-01, Vol.134 (1), p.191-200

1986

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Molecular basis of familial growth hormone-resistant syndromes

Journal of endocrinological investigation (Testo stampato), 1998, Vol.21 (8), p.7-17

1998

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Isolation and chromosomal localization of ecdysterone-responsive genes in a Drosophila cell line

Chromosoma, 1984-01, Vol.89 (5), p.338-342

1984

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Actin gene expression is modulated by ecdysterone in a Drosophila cell line

Journal of molecular biology, 1983-03, Vol.164 (3), p.419-430

1983

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Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells

Syndromic Short Stature in Patients with a Germline Mutation in the LIM Homeobox LHX4

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

Alternatively Spliced Forms in the Cytoplasmic Domain of the Human Growth Hormone (GH) Receptor Regulate Its Ability to Generate a Soluble GH-Binding Protein

Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development

Pituitary stalk interruption syndrome : A clinical-biological-genetic assessment of its pathogenesis

Nine novel growth hormone receptor gene mutations in patients with Laron syndrome

A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH‐binding activity by abolishing receptor homodimerization

Spectrum of growth hormone receptor mutations and associated haplotypes in Laron syndrome

Expression and binding properties of two isoforms of the human growth hormone receptor

Defective Membrane Expression of Human Growth Hormone (GH) Receptor Causes Laron-Type GH Insensitivity Syndrome

A naturally occurring growth hormone receptor mutation : in vivo and in vitro evidence for the functional importance of the WS motif common to all members of the cytokine receptor superfamily

Recurrent nonsense mutations in the growth hormone receptor from patients with Laron Dwarfism

Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalities

Purification of RNA-free plasmid DNA using alkaline extraction followed by ultrogel A2 column chromatography

Molecular study of the retrovirus-like transposable element 412, a 20-OH ecdysone responsive repetitive sequence in Drosophila cultured cells

20-Hydroxyecdysone regulates cytoplasmic actin gene expression in Drosophila cultured cells

20-OH-ecdysone regulates 60 C β tubulin gene expression in Kc cells and during Drosophila development

Evolutionary divergence of the truncated growth hormone receptor isoform in its ability to generate a soluble growth hormone binding protein

Pathologie moléculaire des facteurs de transcription impliqués dans le développement de l'antéhypophyse

Species-specific Alternative Splice Mimicry at the Growth Hormone Receptor Locus Revealed by the Lineage of Retroelements during Primate Evolution. A novel mechanism accounting for protein diversity between and within species

Expression of a new β tubulin subunit is induced by 20-hydroxyecdysone in drosophila cultured cells

Molecular basis of familial growth hormone-resistant syndromes

Isolation and chromosomal localization of ecdysterone-responsive genes in a Drosophila cell line

Actin gene expression is modulated by ecdysterone in a Drosophila cell line

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