戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 noncoding RNAs, modulates risk for TGCTs and testicular abnormalities in both parent-of-origin and co
2 fathead minnow had returned to baseline, and testicular abnormalities were absent.
3 ences, laterality of tumors and incidence of testicular abnormalities, are useful for identification
4           In this study, we identified ACPT (testicular acid phosphatase) biallelic mutations causing
5 ct is highly suggestive for the diagnosis of testicular adrenal rest tissues on ultrasonography.
6  magnetic resonance (MR) imaging features of testicular adrenal rest tumors (TART) in patients with c
7  bilateral testicular masses, a diagnosis of testicular adrenal rest tumour was made; biopsy was defe
8                                              Testicular adrenal rest tumours (TARTs) are benign testi
9                          Prompt diagnosis of testicular adrenal rest tumours is essential, as it only
10  patient was discovered to harbour bilateral testicular adrenal rests as well.
11 niche) to direct non-mammary cells including testicular and embryonic stem cells (ESCs) to adopt a ma
12 nscriptome sequencing of precursor, primary (testicular and mediastinal) and chemoresistant metastati
13 zing hormone (LH) and testosterone levels or testicular and semen volume.
14 testis descent, INSL3 has been implicated in testicular and sperm function in adult males via interac
15 (breast, prostate, ovarian, endometrial, and testicular) and to investigate whether dietary fiber int
16 sue and several cancers, including prostate, testicular, and ovarian.
17           As a consequence, the depletion of testicular androgens in patients with prostate cancer re
18 nut supplemented diet significantly improves testicular antioxidant function and semen quality in old
19 id of endogenous germline but possess normal testicular architecture and somatic cell function capabl
20 mbryonic Sertoli cells (SCs) leads to severe testicular atrophy and male sterility owing to rapid dep
21  However, PRL1(-/-)/PRL2(+/-) male mice show testicular atrophy phenotype similar to PRL2(-/-) mice.
22  At post-natal day 200, random appearance of testicular atrophy was noted in exposed offspring, and l
23  display signs of premature aging, including testicular atrophy, reduced LC and Sertoli cell (SC) num
24 ands attributed to androgen effects, such as testicular atrophy, seminiferous tubule diameter reducti
25 fluence this phenotype, the role of PPARD in testicular biology was examined.
26                        For prepubertal boys, testicular biopsy cryopreservation is offered in some ce
27 s; the most frequently reported cancers were testicular, breast, and lymphoma.
28 5-C associated with increased pancreatic and testicular but decreased lung cancer and melanoma risk,
29 Rs were highest for multiple myeloma (30.5), testicular cancer (17.0), and kidney cancer (12.5); for
30 ardiovascular disease (CVD) in patients with testicular cancer (TC) given chemotherapy in European st
31 etachronous contralateral (second) germ cell testicular cancer (TC).
32 wo), nasopharyngeal (one), thyroid (one) and testicular cancer (two).
33                            The international Testicular Cancer Consortium (TECAC) combined five publi
34  of 5190 men with GCC who entered the Danish Testicular Cancer database between January 1, 1984, and
35                              From the Danish Testicular Cancer database, we identified all patients w
36 Clinical data were extracted from the Danish Testicular Cancer database.
37  we show that fine-mapping of pancreatic and testicular cancer GWAS within one of these loci (Region
38  cisplatin-induced ototoxic effects in adult testicular cancer patients.
39 rmation on adverse health outcomes (AHOs) in testicular cancer survivors (TCSs) after four cycles of
40 s are an important complication that affects testicular cancer survivors as a consequence of treatmen
41 carcinoma, men undergoing surveillance after testicular cancer treatment, parents of patients treated
42 inumab and no deaths and one case of cancer (testicular cancer) among 319 patients who received place
43 .6% aged 25-37 years, 57.4% 38-50 years, 88% testicular cancer, 10% lymphoma, matched for body mass i
44 al cancer, 20.2% (18.9-21.5) in survivors of testicular cancer, 26.6% (24.7-28.6) in female survivors
45 cal cancer, 18.9 (16.6-21.1) in survivors of testicular cancer, 55.7 (50.4-61.1) in female survivors
46 long-term survivors of cervical, breast, and testicular cancer, and Hodgkin lymphoma provides an evid
47 survivors of breast cancer, cervical cancer, testicular cancer, and Hodgkin lymphoma.
48  17 years or older, diagnosed with germ cell testicular cancer, and previously treated with cisplatin
49  2 Diabetes, Breast Cancer, Prostate Cancer, Testicular Cancer, Gallstones, Glaucoma, Gout, Atrial Fi
50  30 years from diagnosis of cervical cancer, testicular cancer, Hodgkin lymphoma in women, breast can
51                Children and adolescents with testicular cancer, leukaemia, and Ewing sarcomas are at
52                            Male survivors of testicular cancer, lymphoma, and leukaemia aged 25-50 ye
53 resence of cardiovascular disease, diabetes, testicular cancer, or prostate cancer.
54 ug reaction in adult patients with germ cell testicular cancer.
55 from 1.1% for pancreatic cancer to 98.2% for testicular cancer.
56 esophageal, laryngeal, Hodgkin lymphoma, and testicular cancer.
57 er; 487518 due to liver cancer; 13927 due to testicular cancer; and 829396 due to non-Hodgkin lymphom
58 ection, ranging from <1/tumor in thyroid and testicular cancers to >10/tumor in endometrial and color
59  genetic impairment of NER, such as skin and testicular cancers.
60 t left inguinal orchiectomy, which disclosed testicular carcinoma composed of 90% choriocarcinoma, 9%
61 ies to assess interactions of SCs with other testicular cells and to test the ability of anti-ZIKV dr
62                                              Testicular cells exhibit similar molecular responses to
63 alyzed single-cell transcriptomes of ~10,000 testicular cells from four boys spanning puberty and com
64       PFOS induces Sertoli cell injury using testicular cells isolated from rodent testes, but it rem
65                                              Testicular cells produce several biologically active pep
66 d from omental fat and lung did not redirect testicular cells to a MEC fate, indicating the necessity
67 studies to explore the interactions of other testicular cells with Sertoli cells and to test novel an
68 can be engrafted from fresh or cryopreserved testicular cells, leading to complete spermatogenesis fr
69 rasite burden, horn length, horn growth, and testicular circumference.
70 r that, magnetic resonance imaging (MRI) and testicular color Doppler ultrasound (CDU) were performed
71                                              Testicular concentrations of DEHP and PCB153 perturbed s
72 yndromes including Crouzon and Pfeiffer, but testicular defects were not reported.
73 e loss of ClC-2 function lead to retinal and testicular degeneration and leukodystrophy, whereas gain
74 on of ClC-2 in mice to show that retinal and testicular degeneration depend on a loss of ClC-2 in ret
75                          Atrophic testes and testicular degeneration were observed in Ppard(-/-) mice
76  to either LCs or SCs were protected against testicular degeneration, demonstrating that age-related
77 lt mice and rats were sufficient to redirect testicular derived cells to produce normal mammary epith
78  are sufficient to direct differentiation of testicular-derived cells and ESCs to form functional mam
79 ing activational roles for ovarian-, but not testicular-, derived hormones in mediating hedonic sensi
80  to heat stress, and therefore, mammals with testicular descent may be at a greater risk in the event
81                   This process revealed that testicular development and spermatogenesis, preputial se
82 cific germline ablation but other aspects of testicular development are normal.
83 srupting chemicals during critical phases of testicular development may be related to poorer semen pa
84 is both necessary and sufficient to initiate testicular development, thereby acting as an upstream re
85 d not compensate for low levels during early testicular development.
86 f both SCs and germ cells during prepubertal testicular development.
87 f RSPO1/Rspo1 in XX humans and mice leads to testicular differentiation and female-to-male sex revers
88                                  In mammals, testicular differentiation is initiated by transcription
89  100 testes of 50 patients with a unilateral testicular disease.
90 her men with similar neurologic features and testicular disease.
91                 Among 46,XX individuals with testicular DSD (TDSD) or ovotesticular DSD (OTDSD), test
92 osure on neonatal testes and its relation to testicular dysfunction in adult offspring.
93 ogenic mRNAs, appropriately modeling primary testicular dysfunction observed in aging men.
94 /or to decreased testosterone resulting from testicular dysfunction.
95  findings provide the first evidence for how testicular dysgenesis can result after normal testis dif
96 ral gray matter atrophy), visual impairment, testicular dysgenesis in males and sudden death at infan
97 DBP, a plasticising chemical known to induce testicular dysgenesis in vivo in rats).
98  Focal dysgenesis is a consistent feature of testicular dysgenesis syndrome (TDS) in humans.
99 stosterone, and is used as a model for human testicular dysgenesis syndrome (TDS).
100                            Features of focal testicular dysgenesis were present in re-aggregated test
101 found to have a 46,XY karyotype with partial testicular dysgenesis.
102 s to identify features consistent with focal testicular dysgenesis.
103 tivities is carried out leading to sustained testicular endocrine function, with gonadal testosterone
104 t species because it occurs within a complex testicular environment characterized by the intimate ass
105                                            A testicular examination was normal.
106                      Here we used an ex vivo testicular explant model and in vivo exposure to determi
107 ppress testosterone synthesis in human fetal testicular explants to an extent greater than that seen
108  low protein diet modified F1 male offspring testicular expression of central epigenetic regulators.
109 L mice had a molecular phenotype with higher testicular expression of Slc34a2 and Trpv5 than wild-typ
110 s; and, in a significant proportion of mice, testicular failure and atrophy with tubule lithiasis, po
111 ble just two decades ago, azoospermia due to testicular failure, including 47,XXY (Klinefelter syndro
112                 Sertoli cells (SCs) regulate testicular fate in the differentiating gonad and are the
113 ther sedentary lifestyle was associated with testicular function (semen quality and reproductive horm
114 e administration altered fetal pituitary and testicular function in ovine male fetuses.
115                                              Testicular function is often impaired even years after t
116   To investigate the involvement of PLAG1 in testicular function, we determined (i) the spatial distr
117 uld be specifically disruptive of ovarian or testicular function, while leaving extragonadal function
118 heir distinct roles in organ homeostasis and testicular function.
119 gulate vitamin D and mineral homeostasis, on testicular function.
120 6 functions in mouse testis determination or testicular function.
121 tion of PFOS on lipid mediators in affecting testicular functions.
122  that PFOS has potential negative impacts on testicular functions.
123 e absence of detectable changes in the intra-testicular GC transcriptome.
124 not find significant changes in the F0 intra-testicular GC transcriptome.
125 om precursor to primary disease, and primary testicular GCTs (TGCTs) are uniformly wild type for TP53
126 ic study, serum samples of 616 patients with testicular GCTs and 258 male controls were examined for
127 NA profiling found that DMRT1 activates many testicular genes and downregulates ovarian genes and sin
128 ides a rich resource for those investigating testicular germ and somatic cell developmental during th
129 tance: Patients given systemic treatment for testicular germ cell cancer (GCC) are at increased risk
130 ence of teratoma in patients with metastatic testicular germ cell tumor (GCT) is of unknown prognosti
131 rognosticate survival outcomes in metastatic testicular germ cell tumor (MT-GCT), but how the initial
132                                Patients with testicular germ cell tumor (TGCT) are at increased risk
133     Genome-wide association (GWA) studies of testicular germ cell tumor (TGCT) have identified 18 sus
134               Unconventional inheritance for testicular germ cell tumor (TGCT) risk both in humans an
135 reported 19 distinct susceptibility loci for testicular germ cell tumor (TGCT).
136 published genome-wide association studies of testicular germ cell tumor (TGCT; 3,558 cases and 13,970
137  and specificity than the classic markers of testicular germ cell tumors (GCTs) and are applicable to
138                                              Testicular germ cell tumors (TGCT) are the most frequent
139 lity is a risk factor for the development of testicular germ cell tumors (TGCT), but the initiating e
140 ed regulatory networks in two major types of testicular germ cell tumors (TGCT): seminoma (SE) and no
141                                              Testicular germ cell tumors (TGCTs) are classified into
142  discusses several important developments in testicular germ cell tumors (TGCTs) over the past year.
143                                              Testicular germ cell tumors (TGCTs) share germline ances
144 ansformed understanding of susceptibility to testicular germ cell tumors (TGCTs), but much of the her
145 ly used anticancer drug for the treatment of testicular germ cell tumors (TGCTs).
146                                              Testicular germ cell tumour (TGCT) is the most common ca
147                        A sizable fraction of testicular germ cell tumour (TGCT) risk is expected to b
148 GWAS) have identified multiple risk loci for testicular germ cell tumour (TGCT), revealing a polygeni
149 ng for >15% of the genetic susceptibility to testicular germ cell tumour (TGCT).
150                                              Testicular germ cell tumours (TGCTs) are the most common
151                                   While most testicular germ cell tumours (TGCTs) exhibit exquisite s
152 also summarise the consensus on how to treat testicular germ cell tumours and focus on a few controve
153                                              Testicular germ cell tumours are at the crossroads of de
154                                              Testicular germ cell tumours are highly sensitive to rad
155 f the epidemiology, genetics, and biology of testicular germ cell tumours.
156 aternal low-protein diet elevates ROS in the testicular germ cells, altering ATF7 activity and H3K9me
157 sues but was the most abundant CL species in testicular germ cells.
158                                Post-pubertal testicular germ-cell tumours (TGCTs) can present with a
159                        We demonstrate that a testicular germ-cell-secreted epidermal growth factor-li
160                                              Testicular global DNA methylation increased, while ovari
161 intrachromosomal inversion involving the pro-testicular growth factor gene FGF9, which is heterochron
162                       Gonadotropin Regulated Testicular Helicase (GRTH/DDX25), expressed in the male
163                         These alterations of testicular histology and gene expression patterns were s
164 sequences of PLAG1 deficiency by determining testicular histology, daily sperm production and sperm m
165 er 16 types of AYA cancer: breast; cervical; testicular; Hodgkin lymphoma (female); Hodgkin lymphoma
166 ssing cells results in a transient impact on testicular homeostasis, with this population behaving st
167   This phenotype appears to be suppressed by testicular hormones in male Prkca(-/-) mice.
168  difference is at least partly maintained by testicular hormones.
169 gene editing to knockout the HMGB4 gene in a testicular human embryonic carcinoma and examined cellul
170 ive oligosaccharides were obtained by bovine testicular hyaluronidase digestion.
171  in cell culture conditions, using zebrafish testicular hyperplasia cells that accumulate early stage
172 ss and varicocele-related infertility due to testicular hyperthermia, which can result in low sperm f
173 rm trial, patients with IR MGCT (stage II-IV testicular, II-III ovarian, I-II extragonadal, or stage
174 s (TM) play an important role in maintaining testicular immune privilege and display reduced proinfla
175         Our results suggest that TM maintain testicular immune privilege by inhibiting NF-kappaB sign
176 dentify SCs as a therapeutic target to clear testicular infections.
177 e equivalent dose of 20 g/m(2) or greater or testicular irradiation with 20 Gy or greater.
178 reast; cervical; uterine; ovarian; prostate; testicular; kidney; bladder; brain and nervous system; t
179  normal testicular tissues as well as benign testicular lesions (P=0.000).
180 t difference between ADC values of malignant testicular lesions and normal testicular tissues as well
181 From January 2012 to December 2015, 55 focal testicular lesions that were indeterminate on gray-scale
182                                Results Of 55 testicular lesions, 43 (78.2%) were benign and 12 (21.8%
183 n differentiating benign and malignant focal testicular lesions.
184 nosis and individualized management of small testicular lesions.
185                                              Testicular Leydig cells (LCs) are the primary source of
186 axin/insulin superfamily and is expressed in testicular Leydig cells.
187 us system (CNS) lymphoma (PCNSL) and primary testicular lymphoma (PTL) are rare extranodal large B-ce
188 ervous system lymphomas (PCNSLs) and primary testicular lymphomas (PTLs) are extranodal large B-cell
189                                              Testicular macrophages (TM) play an important role in ma
190                                              Testicular macrophages (tMphi) are the principal immune
191 with X-linked ichthyosis, corneal opacities, testicular maldescent, cardiac arrhythmia, and higher ra
192 on of gonads, significant down-regulation of testicular markers Amh and Sox9, and remarkable up-regul
193 previously healthy man presented with a left testicular mass, confirmed on ultrasound.
194 .A healthy 27-year-old man discovered a left testicular mass.
195 ular adrenal rest tumours (TARTs) are benign testicular masses that are found in inadequately treated
196  typical sonographic appearance of bilateral testicular masses, a diagnosis of testicular adrenal res
197 that the impacts of persistent pollutants on testicular maturation and function require further inves
198 separate intrinsic LC aging from that of the testicular microenvironment in vivo has made this questi
199                                      A Young testicular microenvironment protects Leydig cells agains
200 is largely driven by aging of the supporting testicular microenvironment.
201 lusion There is a strong association between testicular microlithiasis and primary testicular neoplas
202 y define the strength of association between testicular microlithiasis and testicular neoplasia in a
203                                              Testicular microlithiasis was present in 4 of 9 patients
204                                              Testicular microvessels and blood flow are known to cont
205                   Hence HTPCs via control of testicular microvessels may contribute to the regulation
206 23 and Klotho influence gonadal function and testicular mineral ion homeostasis both directly and ind
207 Cul4bled to male infertility, despite normal testicular morphology and comparable numbers of spermato
208 iation between testicular microlithiasis and testicular neoplasia in a large geographically diverse p
209 etween testicular microlithiasis and primary testicular neoplasia in this pediatric population.
210 ive and developmental stages to populate the testicular niche prior to productive spermatogenesis.
211 rs) were calculated for 15,006 patients with testicular nonseminoma reported to the population-based
212 gh prevalence of TP53 mutations not found in testicular nonseminomas.
213                 Active surveillance (AS) for testicular nonseminomatous germ cell tumors (NSGCT) is w
214 46,XX karyotype develop testes or ovotestes (testicular or ovotesticular disorder of sex development;
215 gely used as an anti-cancerous agent against testicular, ovarian, small cell lung, colon and breast c
216 tation causing isolated, non-syndromic 46,XX testicular/ovotesticular DSD in humans.
217 ascularity was observed in the heterogeneous testicular parenchyma.
218                               Although gross testicular pathology was not seen, the demonstrated brea
219     Our proteomic study using cultured human testicular peritubular cells (HTPCs) i.e. the cells, whi
220                                         Thus testicular peritubular cells, via PEDF, may prevent vasc
221 ence of modifier genes which exacerbated the testicular phenotype.
222 rmates, which suggests a regulatory role for testicular phosphate and calcium homeostasis.
223 rences in temperature-sensitive expressions, testicular physiology, spermatogenesis, as well as its r
224 al carcinoma and rete testis invasion in the testicular primary identified a group with a relapse ris
225 d an age of 26 years or older at assessment, testicular radiotherapy at any dose, and alkylating agen
226 sk increased with older age, higher doses of testicular radiotherapy, and cyclophosphamide equivalent
227                                   Older age, testicular radiotherapy, and exposure to alkylating agen
228 ermatogonia that are essential for efficient testicular regeneration after injury.
229 blation of Sox8 and Sox9 prevents ovarian-to-testicular reprogramming observed in XX Rspo1 loss-of-fu
230                    We find that DMRT1 blocks testicular retinoic acid (RA) signaling from activating
231               Knowledge of the regulation of testicular retinoic acid synthesis is crucial for unders
232                       Gonadotropin-regulated testicular RNA helicase (GRTH/DDX25) is a testis specifi
233  a complex delayed diagnosed example case of testicular rupture clinically mimicing epididymo-orchiti
234                           Early diagnosis of testicular rupture may lead to the salvaging of the test
235                                              Testicular rupture may occur even after moderate sportiv
236 blunt trauma may result in injuries, such as testicular rupture, dislocation, torsion, hematoma, sper
237  time, leptin as a key factor able to affect testicular seminoma behavior, highlighting leptin recept
238 s receptor was significantly higher in human testicular seminoma compared with normal adult testis.
239 arkers, their potential involvement in human testicular seminoma growth and progression remains unexp
240 s into either ovarian pre-granulosa cells or testicular Sertoli cells.
241 velopment of ProSG, their SG descendants and testicular somatic cells during the perinatal period in
242  cases when combining surgical harvesting of testicular sperm and ICSI.
243                                         Post-testicular sperm maturation, in which sperm centrioles f
244                                           In testicular sperm, tRNA fragments are scarce but increase
245                                    Following testicular spermatogenesis, mammalian sperm continue to
246 iarrheic pig from Ohio was isolated in swine testicular (ST) and LLC porcine kidney (LLC-PK) cell cul
247 F3 DEHP males exhibited decreased fertility, testicular steroidogenic capacity, and spermatogenesis t
248 suppress gonadotropins, thereby blocking the testicular T production needed for spermatogenesis, whil
249                                              Testicular teratocarcinoma cells rarely contain mutation
250 t new therapeutic possibilities of targeting testicular teratocarcinoma.
251 s, whereas male genital development required testicular testosterone plus dihydrotestosterone (DHT) m
252 ravity on Earth disrupts spermatogenesis and testicular testosterone synthesis in rodents, whereas th
253                          Cryopreservation of testicular tissue allows storage of early sperm precurso
254 orage aimed at subsequent transplantation of testicular tissue and associated stem cells.
255 loped a protocol to cryopreserve rainbowfish testicular tissue and recover an enriched population of
256                                              Testicular tissue cryopreservation is an experimental me
257 lts are obtained in noncastrated recipients, testicular tissue grafting may be applied in the clinic.
258  occurs in parallel with the degeneration of testicular tissue in the ovotestis and enhanced ovarian
259 lar DSD (TDSD) or ovotesticular DSD (OTDSD), testicular tissue is present in the gonad.
260 All lesions appeared hypointense compared to testicular tissue on T1W and T2W magnetic resonance imag
261 their female equivalents-granulosa cells-and testicular tissue reorganizes to a more ovarian morpholo
262         Only 12% of the genetic males showed testicular tissue six months after fertilization.
263           Expression of TTBKs is enriched in testicular tissue, but their relevance to reproductive p
264 ion of apoptosis-related genes (P < 0.05) in testicular tissue.
265 s of malignant testicular lesions and normal testicular tissues as well as benign testicular lesions
266  of principle that cryopreserved prepubertal testicular tissues can be autologously grafted under the
267 compared to average risk, ranges from 12 for testicular to 2.5 for ovarian cancer.
268 GWAS heritability vary from 60,000 cases for testicular to over 1,000,000 cases for lung cancer.
269                                 Extravaginal testicular torsion (ETT), also called prenatal or perina
270                                              Testicular torsion may concern boys even in the perinata
271                                              Testicular torsion must be taken into consideration in d
272                                            A testicular torsion was suspected, so the baby underwent
273 auxiliary method in the diagnosis of partial testicular torsion.
274 ul tool in the early diagnosis of incomplete testicular torsion.
275 ficient (ADC) in the diagnosis of incomplete testicular torsion.
276 ticle affected and 2 patients with bilateral testicular torsion.
277 chitis and radiologically mimicing traumatic testicular torsion.
278 ency surgical treatment, required in case of testicular torsion.
279 ates include hydrocoele, inguinal hernia and testicular torsion; less common is epididymo-orchitis.
280       Studies also suggest that BPA may be a testicular toxicant in animal models, but the data in hu
281                                      Indeed, testicular transcriptome analysis found that a number of
282 ersity between 1990 and 2016 and had primary testicular tumor specimen from orchiectomy (ORCH) were i
283 GSG does not translate to higher efficacy of testicular tumorigenesis arising from mutant p53 cells,
284 reprogramming in both normal development and testicular tumorigenesis.
285 ata bases were searched for pathology-proven testicular tumors (benign or malignant germ cell or stro
286  test was used to analyze the association of testicular tumors and TM.
287                                       Benign testicular tumors are frequent incidental findings.
288 ions or microlithiasis and all patients with testicular tumors from pathology database were identifie
289                                              Testicular tumors, the most common cancer in young men,
290 lurality of suicides is from hematologic and testicular tumors; if > 50, from prostate, lung, and col
291  p53 is a common finding in most cancers but testicular tumours accumulate wild-type p53 (wtp53).
292 accompanied by increased G-CSF signaling and testicular vacuolation associated with decreased fertili
293                                       Normal testicular vessels coursing through the lesions undistur
294             Doppler ultrasound showed normal testicular vessels passing through the mass which were u
295 th, Tanner stage 5 for pubic hair growth, or testicular volume (TV) >/= 20 mL in either testis.
296 al staging [genitalia (G), pubarche (P), and testicular volume (TV)].
297 d to assess reproductive endocrine function, testicular volume, semen quality, and fertility in adult
298               Treatment with FGF23 increased testicular weight in wild-type mice, while mice with glo
299 lobal loss of either FGF23 or Klotho had low testicular weight, reduced sperm count, and sperm motili
300 ls and to test novel antivirals for clearing testicular ZIKV infection.

 
Page Top