Results 141 to 150 of about 5,621 (166)

Multiplexed Imaging Mass Cytometry Reveals Tumor-immune Microenvironment-dependent Hormone Receptor Expression in Adult-Type Ovarian Granulosa Cell Tumors. [PDF]

Cancer Res Commun
Khlebus EY, Vuttaradhi VK, Ferri-Borgogno S, Brodsky AL, Lawson BC, Mok SC, Hillman RT.   +6 more
europepmc   +1 more source

Evaluation of season and sex specific differential gonadal transcriptomics in Himalayan snow trout Schizothorax plagiostomus, Heckel, 1838. [PDF]

Sci Rep
Bhattacharya I, Kothandaraman H, Kothiyal S, Sharma P, Purohit S, Anitha A, Agarwal NK.   +6 more
europepmc   +1 more source

A phase II study of androgen receptor inhibition by darolutamide in combination with leuprolide acetate and exemestane in recurrent adult-type ovarian granulosa cell tumor. [PDF]

Gynecol Oncol
Hopp EE, Enserro D, Campos S, Chitiyo V, Huang G, Lankes H, Crane EK, Hoekstra A, Siedel J, Richardson DL, Aghajanian C, Rader JS, Covens A.   +12 more
europepmc   +1 more source

Study of <i>FOXL2</i> Regulation on Ovarian Function in <i>Chlamys farreri</i> Through Comparative ChIP-Seq and Transcriptome Analysis Using RNA Interference. [PDF]

Biology (Basel)
Liu X, Yun H, Xing Y, Wang S, Zhou X, Zhang J.   +5 more
europepmc   +1 more source

Myoid Gonadal Stromal Tumor of the Testis: A Rare Sex Cord-Stromal Neoplasm in a Young Man. [PDF]

Cureus
Morton EA, Nieder SR, Abdollahzadeh A, Davis D, Sina J, Mullane P, Lahiji R, Browne B.   +7 more
europepmc   +1 more source

Roles of Binding Elements, FOXL2 Domains, and Interactions With cJUN and SMADs in Regulation of FSHβ [PDF]

Molecular Endocrinology, 2014
We previously identified FOXL2 as a critical component in FSHβ gene transcription. Here, we show that mice deficient in FOXL2 have lower levels of gonadotropin gene expression and fewer LH- and FSH-containing cells, but the same level of other pituitary ...
Kellie M Breen, Pamela L Mellon, Djurdjica Coss   +2 more
exaly   +2 more sources

FOXL2 mutations and genomic rearrangements in BPES†

Human Mutation, 2009
The FOXL2 gene is one of 10 forkhead genes, the mutations of which lead to human developmental disorders, often with ocular manifestations. Mutations in FOXL2 are known to cause blepharophimosis syndrome (BPES), an autosomal. dominant eyelid malformation
Elfride De Baere, Diane Beysen
exaly   +2 more sources

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Function of Foxl2 and Dmrt1 proteins during gonadal differentiation in the olive flounder

International Journal of Biological Macromolecules, 2022
Congcong Zou, Lingming Kong
exaly  

FOXL2 Interacts with Steroidogenic Factor-1 (SF-1) and Represses SF-1-Induced CYP17 Transcription in Granulosa Cells

Molecular Endocrinology, 2010
Kangseok Lee, Miae Won, Jeehyeon Bae
exaly