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PMID |
Sentence |
1 |
727728
|
A 63-year-old woman with longstanding spastic paraplegia and neurological evidence of long tract disturbance was found to have hypothyroidism, partial diabetes insipidus, hyperprolactinemia, and gonadotropin deficiency of hypothalamic origin.
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2 |
7958084
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[Isolated gonadotropin deficiency and secretory discrepancy of cortisol and adrenal androgen by hemochromatosis secondary to congenital dyserythropoietic anemia].
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3 |
7958084
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Serological and hematological examinations revealed that she suffered from hemochromatosis secondary to congenital dyserythropoietic anemia (CDA), characterized by ineffective hematopoiesis and erythropoietic dysplasia.
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4 |
8180439
|
Unusual combination of insulin-dependent diabetes mellitus with transient-pituitary-isolated gonadotropin deficiency.
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5 |
8180439
|
We report a 27-year-old man with insulin-dependent diabetes mellitus and transient-pituitary-isolated gonadotropin deficiency.
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6 |
8180439
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We suspected that both insulin-dependent diabetes mellitus and transient-gonadotropin-deficiency might be an autoimmune mechanism.
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7 |
8180439
|
Unusual combination of insulin-dependent diabetes mellitus with transient-pituitary-isolated gonadotropin deficiency.
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8 |
8180439
|
We report a 27-year-old man with insulin-dependent diabetes mellitus and transient-pituitary-isolated gonadotropin deficiency.
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9 |
8180439
|
We suspected that both insulin-dependent diabetes mellitus and transient-gonadotropin-deficiency might be an autoimmune mechanism.
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10 |
8180439
|
Unusual combination of insulin-dependent diabetes mellitus with transient-pituitary-isolated gonadotropin deficiency.
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11 |
8180439
|
We report a 27-year-old man with insulin-dependent diabetes mellitus and transient-pituitary-isolated gonadotropin deficiency.
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12 |
8180439
|
We suspected that both insulin-dependent diabetes mellitus and transient-gonadotropin-deficiency might be an autoimmune mechanism.
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13 |
9667058
|
The most relevant clinical aspects of hyperprolactinemia, acromegaly, Cushing's disease, secondary hyperthyroidism, syndrome of inappropriate ADH secretion, panhypopituitarism, growth hormone deficiency, gonadotropin deficiency, ACTH deficiency, TSH deficiency, and diabetes insipidus are discussed.
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14 |
9747063
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Insulin resistance in patients with Klinefelter's syndrome and idiopathic gonadotropin deficiency.
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15 |
12083815
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Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene.
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16 |
12083815
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A boy with adrenal hypoplasia congenita (AHC) and multiple pituitary hormone deficiency (MPHD), without mutations in the DAX1 or SF1 genes, is described.
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17 |
12083815
|
Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene.
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18 |
12083815
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A boy with adrenal hypoplasia congenita (AHC) and multiple pituitary hormone deficiency (MPHD), without mutations in the DAX1 or SF1 genes, is described.
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19 |
12704802
|
Many of the observed differences, including down-regulation of collagen type I and collagen-processing enzymes, reflect expected patterns and support the relevance of our results.
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20 |
12704802
|
These include an orphan nuclear receptor DAX1 and a small ras-related GTPase associated with diabetes, both of which increased with increasing differentiation, as well as a high mobility group-box transcription factor, SOX4, that was down-regulated during differentiation.
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21 |
12727972
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We have synthesized the human N-terminal POMC fragment 1-28-POMC with the disulfide bridges in the correct position between cysteine residues 2-24 and 8-20 and studied the activity of these peptides in adrenocortical tumor cells in vitro. 1-28-POMC stimulated cell proliferation in human NCI-h295 and mouse Y-1 adrenal cancer cell lines and also in primary cultures of bovine adrenocortical cells in a concentration-dependent manner. 1-28-POMC led to rapid activation of the MAPKs extracellular signal-regulated kinases-1 and -2, but not c-Jun N-terminal kinase and p38, pathways.
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22 |
12727972
|
However, protein levels of important regulators of steroidogenesis [steroidogenic factor-1, DAX-1 (dosage-sensitive sex reversal-adrenal hypoplasia congenita critical region on the X-chromosome 1), steroidogenic acute regulatory protein, and cytochrome P450 side-chain cleavage enzyme] remained unaffected by 1-28-POMC treatment.
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23 |
16353672
|
In contrast, increased insulin resistance was found in both hypergonadotropic and hypogonadotropic men with hypoandrogenism, patients with Klinefelter's syndrome and men with idiopathic gonadotropin deficiency.
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24 |
16786802
|
Endocrine tests demonstrated a growth hormone and gonadotropin deficiency with diabetes insipidus.
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25 |
19000767
|
Thyroid hormones exert most of their physiological effects through two thyroid hormone receptor (TR) subtypes, TRalpha and TRbeta, which associate with many transcriptional coregulators to mediate activation or repression of target genes.
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26 |
19000767
|
Here, we present a new methodology which employs surface plasmon resonance to investigate the interactions between TRbeta ligand binding domain (LBD) complexes and peptides derived from the nuclear receptor interaction motifs of two of its coregulators, SRC2 and DAX1.
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27 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
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28 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
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29 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
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30 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
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31 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
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32 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
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33 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
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34 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
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35 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
36 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
37 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
38 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
39 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
40 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
41 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
42 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
43 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
44 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
45 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
46 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
47 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
48 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
49 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
50 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
51 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
52 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
53 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
54 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
55 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
56 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
57 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
58 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
59 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
60 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
61 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
62 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
63 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
64 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
65 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
66 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
67 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
68 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
69 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
70 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
71 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
72 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
73 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
74 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
75 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
76 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
77 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
78 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
79 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
80 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
81 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
82 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
83 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
84 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
85 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
86 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
87 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
88 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
89 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
90 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
91 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
92 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
93 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
94 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
95 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
96 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
97 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
98 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
99 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
100 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
101 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
102 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
103 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
104 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
105 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
106 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
107 |
19188450
|
Dax-1 and steroid receptor RNA activator (SRA) function as transcriptional coactivators for steroidogenic factor 1 in steroidogenesis.
|
108 |
19188450
|
The atypical orphan nuclear receptor Dax-1 binds to SF-1 and represses SF-1 target genes.
|
109 |
19188450
|
Paradoxically, however, loss-of-function mutations of Dax-1 also cause adrenal hypoplasia, suggesting that Dax-1 may function as an SF-1 coactivator under some circumstances.
|
110 |
19188450
|
Indeed, we found that Dax-1 can function as a dosage-dependent SF-1 coactivator.
|
111 |
19188450
|
Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that functions as an RNA.
|
112 |
19188450
|
The coactivator TIF2 also associates with Dax-1 and synergistically coactivates SF-1 target gene transcription.
|
113 |
19188450
|
Coactivation by Dax-1 is abolished by SRA knockdown.
|
114 |
19188450
|
The expression of the steroidogenic gene products steroidogenic acute regulatory protein (StAR) and melanocortin 2 receptor is reduced in adrenal Y1 cells following the knockdown of endogenous SRA.
|
115 |
19188450
|
Similarly, the knockdown of endogenous Dax-1 downregulates the expression of the steroidogenic gene products CYP11A1 and StAR in both H295R adrenal and MA-10 Leydig cells.
|
116 |
19188450
|
These findings reveal novel functions of SRA and Dax-1 in steroidogenesis and adrenal biology.
|
117 |
21318063
|
A diagnosis of central diabetes insipidus (CDI) accompanied by growth hormone (GH) and gonadotropin deficiency was made.
|
118 |
23589295
|
Insulin directly regulates steroidogenesis via induction of the orphan nuclear receptor DAX-1 in testicular Leydig cells.
|
119 |
23589295
|
In this study, we found that insulin directly binds to insulin receptors in Leydig cell membranes and activates phospho-insulin receptor-β (phospho-IR-β), phospho-IRS1, and phospho-AKT, leading to up-regulation of DAX-1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) gene expression in the MA-10 mouse Leydig cell line.
|
120 |
23589295
|
Insulin also inhibits cAMP-induced and liver receptor homolog-1 (LRH-1)-induced steroidogenic enzyme gene expression and steroidogenesis.
|
121 |
23589295
|
In contrast, knockdown of DAX-1 reversed insulin-mediated inhibition of steroidogenesis.
|
122 |
23589295
|
In insulin-injected mouse models, insulin receptor signal pathway was activated and subsequently inhibited steroidogenesis via induction of DAX-1 without significant change of luteinizing hormone or FSH levels.
|
123 |
23589295
|
Insulin-mediated induction of DAX-1 in Leydig cells of testis may be a key regulatory step of serum sex hormone level in insulin-resistant states.
|
124 |
23589295
|
Insulin directly regulates steroidogenesis via induction of the orphan nuclear receptor DAX-1 in testicular Leydig cells.
|
125 |
23589295
|
In this study, we found that insulin directly binds to insulin receptors in Leydig cell membranes and activates phospho-insulin receptor-β (phospho-IR-β), phospho-IRS1, and phospho-AKT, leading to up-regulation of DAX-1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) gene expression in the MA-10 mouse Leydig cell line.
|
126 |
23589295
|
Insulin also inhibits cAMP-induced and liver receptor homolog-1 (LRH-1)-induced steroidogenic enzyme gene expression and steroidogenesis.
|
127 |
23589295
|
In contrast, knockdown of DAX-1 reversed insulin-mediated inhibition of steroidogenesis.
|
128 |
23589295
|
In insulin-injected mouse models, insulin receptor signal pathway was activated and subsequently inhibited steroidogenesis via induction of DAX-1 without significant change of luteinizing hormone or FSH levels.
|
129 |
23589295
|
Insulin-mediated induction of DAX-1 in Leydig cells of testis may be a key regulatory step of serum sex hormone level in insulin-resistant states.
|
130 |
23589295
|
Insulin directly regulates steroidogenesis via induction of the orphan nuclear receptor DAX-1 in testicular Leydig cells.
|
131 |
23589295
|
In this study, we found that insulin directly binds to insulin receptors in Leydig cell membranes and activates phospho-insulin receptor-β (phospho-IR-β), phospho-IRS1, and phospho-AKT, leading to up-regulation of DAX-1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) gene expression in the MA-10 mouse Leydig cell line.
|
132 |
23589295
|
Insulin also inhibits cAMP-induced and liver receptor homolog-1 (LRH-1)-induced steroidogenic enzyme gene expression and steroidogenesis.
|
133 |
23589295
|
In contrast, knockdown of DAX-1 reversed insulin-mediated inhibition of steroidogenesis.
|
134 |
23589295
|
In insulin-injected mouse models, insulin receptor signal pathway was activated and subsequently inhibited steroidogenesis via induction of DAX-1 without significant change of luteinizing hormone or FSH levels.
|
135 |
23589295
|
Insulin-mediated induction of DAX-1 in Leydig cells of testis may be a key regulatory step of serum sex hormone level in insulin-resistant states.
|
136 |
23589295
|
Insulin directly regulates steroidogenesis via induction of the orphan nuclear receptor DAX-1 in testicular Leydig cells.
|
137 |
23589295
|
In this study, we found that insulin directly binds to insulin receptors in Leydig cell membranes and activates phospho-insulin receptor-β (phospho-IR-β), phospho-IRS1, and phospho-AKT, leading to up-regulation of DAX-1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) gene expression in the MA-10 mouse Leydig cell line.
|
138 |
23589295
|
Insulin also inhibits cAMP-induced and liver receptor homolog-1 (LRH-1)-induced steroidogenic enzyme gene expression and steroidogenesis.
|
139 |
23589295
|
In contrast, knockdown of DAX-1 reversed insulin-mediated inhibition of steroidogenesis.
|
140 |
23589295
|
In insulin-injected mouse models, insulin receptor signal pathway was activated and subsequently inhibited steroidogenesis via induction of DAX-1 without significant change of luteinizing hormone or FSH levels.
|
141 |
23589295
|
Insulin-mediated induction of DAX-1 in Leydig cells of testis may be a key regulatory step of serum sex hormone level in insulin-resistant states.
|
142 |
23589295
|
Insulin directly regulates steroidogenesis via induction of the orphan nuclear receptor DAX-1 in testicular Leydig cells.
|
143 |
23589295
|
In this study, we found that insulin directly binds to insulin receptors in Leydig cell membranes and activates phospho-insulin receptor-β (phospho-IR-β), phospho-IRS1, and phospho-AKT, leading to up-regulation of DAX-1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) gene expression in the MA-10 mouse Leydig cell line.
|
144 |
23589295
|
Insulin also inhibits cAMP-induced and liver receptor homolog-1 (LRH-1)-induced steroidogenic enzyme gene expression and steroidogenesis.
|
145 |
23589295
|
In contrast, knockdown of DAX-1 reversed insulin-mediated inhibition of steroidogenesis.
|
146 |
23589295
|
In insulin-injected mouse models, insulin receptor signal pathway was activated and subsequently inhibited steroidogenesis via induction of DAX-1 without significant change of luteinizing hormone or FSH levels.
|
147 |
23589295
|
Insulin-mediated induction of DAX-1 in Leydig cells of testis may be a key regulatory step of serum sex hormone level in insulin-resistant states.
|