(Q24643438)

2

0 references

Zvi U Borochowitz

3

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Marina Okopnik

4

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Carlos Knopf

5

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Margarita Indelman

6

0 references

Arie Drugan

7

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Dov Tiosano

8

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Ruth Gershoni-Baruch

9

0 references

Mordechai Choder

10

0 references

Eli Sprecher

American Journal of Human Genetics

11

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language of work or name

English

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publication date

January 2008

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published in

0 references

volume

82

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issue

1

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page(s)

39-47

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cites work

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A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman

7 April 2017

1 reference

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Sex reversal by loss of the C-terminal transactivation domain of human SOX9

7 April 2017

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The Wnt signaling pathway in development and disease

7 April 2017

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The highways and byways of mRNA decay

7 April 2017

1 reference

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Wnt/beta-catenin signaling acts upstream of N-myc, BMP4, and FGF signaling to regulate proximal-distal patterning in the lung

7 April 2017

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Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

7 April 2017

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Female development in mammals is regulated by Wnt-4 signalling

7 April 2017

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Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4

7 April 2017

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Beta-catenin regulates differentiation of respiratory epithelial cells in vivo

7 April 2017

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Wnt-4 deficiency alters mouse adrenal cortex function, reducing aldosterone production

7 April 2017

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Matrix metalloproteinases and the regulation of tissue remodelling

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Canonical WNT signaling during kidney development

7 April 2017

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Genetic approaches to human renal agenesis/hypoplasia and dysplasia

27 September 2017

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Epithelial stem cells: turning over new leaves

27 September 2017

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Wnt signalling: variety at the core.

27 September 2017

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R-spondin1 is essential in sex determination, skin differentiation and malignancy.

27 September 2017

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Wnt4 action in gonadal development and sex determination

27 September 2017

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Balancing the bipotential gonad between alternative organ fates: a new perspective on an old problem

27 September 2017

1 reference

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Genetic analysis of adrenal absence: agenesis and aplasia

27 September 2017

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The pathway to femaleness: current knowledge on embryonic development of the ovary

27 September 2017

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

27 September 2017

1 reference

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Mutational analysis of SRY in XY females

27 September 2017

1 reference

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Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene

27 September 2017

1 reference

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Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

30 May 2018

1 reference

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The partial female to male sex reversal in Wnt-4-deficient females involves induced expression of testosterone biosynthetic genes and testosterone production, and depends on androgen action.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253972

Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253972

Gas chromatography-mass spectrometry profiling of steroids in times of molecular biology

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18179883

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.AJHG.2007.08.005

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2007.08.005

1 reference

1 reference

1 reference

PubMed publication ID

18179883

1 reference