FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

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A Combined PLS and Negative Binomial Regression Model for Inferring Association Networks from Next-generation Sequencing Count Data.Novel action of FOXL2 as mediator of Col1a2 gene autoregulation.Genetic mapping of principal components of canine pelvic morphology.

P2860

Q31161072-76437A76-0DED-4F86-9382-E1A9946E54E0 Q33926240-DE6710CD-8948-4686-9EAB-5B1CA9DBAC8C Q37719570-36A60888-8F99-4D63-8B6B-E8547B49CE97

P2860

FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

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FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

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FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

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FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

@ast

FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

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FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

@ast

FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

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P1476

FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

@en

P2093

Alessandro Puddu

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Angela Loi

http://www.w3.org/2001/XMLSchema#string

Antonino Forabosco

http://www.w3.org/2001/XMLSchema#string

Emanuele Pelosi

http://www.w3.org/2001/XMLSchema#string

Loredana Marcia

http://www.w3.org/2001/XMLSchema#string

Manila Deiana

http://www.w3.org/2001/XMLSchema#string

Mara Marongiu

http://www.w3.org/2001/XMLSchema#string

Mario Lovicu

http://www.w3.org/2001/XMLSchema#string

Yonqing Zhang

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P2860

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

A clinical and genetic study of campomelic dysplasia.

Specification of jaw subdivisions by Dlx genes

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

Somatic sex reprogramming of adult ovaries to testes by FOXL2 ablation

The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance

Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

Foxl2 is required for commitment to ovary differentiation

Estrogen deficiency, obesity, and skeletal abnormalities in follicle-stimulating hormone receptor knockout (FORKO) female mice

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s12861-015-0072-y

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scholarly article

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10.1186/S12861-015-0072-Y

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David Schlessinger

Manuela Uda

Laura Crisponi

P577

2015-07-02T00:00:00Z

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279530505

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4489133

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FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

about

P2860

P2860

FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P5875

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P5875

P6179

P698

P932