(Q28237330)

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M Fukami

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B Niesler

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A Mertz

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G Binder

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S Kirsch

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M Winkelmann

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G Nordsiek

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U Heinrich

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M H Breuning

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M B Ranke

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A Rosenthal

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T Ogata

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G A Rappold

Growth hormone receptor and serum binding protein: purification, cloning and expression

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language of work or name

English

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publication date

May 1997

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54-63

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cites work

1 reference

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

21 April 2017

1 reference

Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene

21 April 2017

1 reference

Cloning and characterization of four murine homeobox genes

21 April 2017

1 reference

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

21 April 2017

1 reference

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

21 April 2017

1 reference

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

21 April 2017

1 reference

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

21 April 2017

1 reference

A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal

21 April 2017

1 reference

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome

21 April 2017

1 reference

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 April 2017

1 reference

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

21 January 2018

1 reference

Fibroblast-growth-factor receptor mutations in human skeletal disorders

21 January 2018

1 reference

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

21 January 2018

1 reference

Characterization of a YAC contig spanning the pseudoautosomal region

21 January 2018

1 reference

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.

21 January 2018

1 reference

Mammalian sex determination: thumbs down for zinc finger?

21 January 2018

1 reference

X-chromosome inactivation may explain the difference in viability of XO humans and mice

21 January 2018

1 reference

XO monosomy is associated with reduced birthweight and lowered weight gain in the mouse

21 January 2018

1 reference

PROSITE: a dictionary of sites and patterns in proteins

21 January 2018

1 reference

Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector

21 January 2018

1 reference

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification

21 January 2018

1 reference

Human Growth Hormone: Complementary DNA Cloning and Expression in Bacteria

21 January 2018

1 reference

7 January 2021

Molecular basis for familial isolated growth hormone deficiency

1 reference

7 January 2021

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

7 January 2021

Towards a consensus on the definition of idiopathic short stature

1 reference

7 January 2021

Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height

1 reference

7 January 2021

A SYNDROME OF INFANTILISM, CONGENITAL WEBBED NECK, AND CUBITUS VALGUS1

1 reference

7 January 2021

The role of Yp in sex determination: new evidence from X/Y translocations

1 reference

7 January 2021

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

1 reference

7 January 2021

A high resolution deletion map of human chromosome Xp22.

1 reference

7 January 2021

Short stature in a girl with partial monosomy of the pseudoautosomal region distal to DXYS15: further evidence for the assignment of the critical region for a pseudoautosomal growth gene(s).

1 reference

7 January 2021

Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries

1 reference

7 January 2021

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

1 reference

7 January 2021

Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid

1 reference

7 January 2021

Limb mesenchymal cells inhibited from undergoing cartilage differentiation by a tumor promoting phorbol ester maintain expression of the homeobox-containing gene Msx1 and fail to exhibit gap junctional communication

1 reference

7 January 2021

Up-regulation of HOXC6, HOXD1, and HOXD8 homeobox gene expression in human neuroblastoma cells following chemical induction of differentiation

1 reference

7 January 2021

A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivation

1 reference

7 January 2021

Recommendations for Diagnosis, Treatment, and Management of Individuals with Turner Syndrome

1 reference

7 January 2021

Turner syndrome resulting from partial deletion of Y chromosome short arm: localization of male determinants

1 reference

7 January 2021

Small deletions of the short arm of the Y chromosome in 46,XY females

1 reference

7 January 2021

Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females

1 reference

7 January 2021

Chromosomal localisation of a gene(s) for Turner stigmata on Yp.

1 reference

7 January 2021

Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata

1 reference

7 January 2021

The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouse

1 reference

7 January 2021

Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes

1 reference

7 January 2021

The GTPase dynamin binds to and is activated by a subset of SH3 domains

1 reference

7 January 2021

Identification of a ten-amino acid proline-rich SH3 binding site

1 reference

7 January 2021

Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23.

1 reference

7 January 2021

The Y specific growth gene(s): how does it promote stature?

1 reference

7 January 2021

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

1 reference

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

7 January 2021