1 s underlying testicular immune privilege and
intratesticular allograft survival remain unclear.
2 Temporal profiles of
intratesticular androgens alongside the expression of st
3 abnormalities are associated with increased
intratesticular BA levels in general and deoxycholic aci
4 Color Doppler US demonstrated
intratesticular blood flow in 60 (88%) testes.
5 Power Doppler US demonstrated
intratesticular blood flow in 66 (97%) testes.
6 Intratesticular blood flow was graded as follows: 0, no
7 ve than color Doppler US in the detection of
intratesticular blood flow.
8 CD40L costimulation induced the tolerance of
intratesticular,
but not renal subcapsular, islet allogr
9 intratesticular varicoceles and other benign
intratesticular cystic lesions are also discussed.
10 llows: 0, no intratesticular flow; 1, single
intratesticular Doppler signal identified; and 2, multip
11 r Doppler signal identified; and 2, multiple
intratesticular Doppler signals identified.
12 whether the immunoprotection afforded by the
intratesticular environment is potent enough to prevent
13 Doppler US better depicted differences in
intratesticular flow between torsed and normal testes.
14 The symmetry of
intratesticular flow was assessed both subjectively and
15 ular blood flow was graded as follows: 0, no
intratesticular flow; 1, single intratesticular Doppler
16 We found that CD8 memory T cells reject
intratesticular grafts at a significantly slower rate th
17 microlithiasis, intratesticular masses, and
intratesticular heterogeneous changes.
18 n be triggered by various stimuli, including
intratesticular hormone deprivation.
19 hibitor) or anti-beta1-integrin antibody via
intratesticular injection indeed delayed AF-2364-induced
20 ogenesis worsened with age despite unchanged
intratesticular iron levels.
21 Despite the immune regulation,
intratesticular islet allografts all were rejected withi
22 Tolerance to
intratesticular islet allografts spread to skin allograf
23 ation is essential for prolonged survival of
intratesticular islet allografts, as blocking PD-L1 or P
24 r immune privilege and long-term survival of
intratesticular islet allografts.
25 e antigen 4, abrogated long-term survival of
intratesticular islet allografts.
26 e following treatments for 5 days: (i) daily
intratesticular (
IT) injections with saline (control); (
27 tient with a focal, nonpalpable, hypoechoic,
intratesticular lesion, a history of testicular biopsy s
28 able differentiation of benign and malignant
intratesticular lesions and can potentially be useful in
29 trast agent-enhanced US in the assessment of
intratesticular lesions.
30 yp19 expression was accompanied by increased
intratesticular levels of estradiol.
31 Intratesticular mass always is a concern, and heterogene
32 Testicular US revealed
intratesticular mass in 15, heterogeneous changes in 11,
33 All were hypoechoic except for one
intratesticular mass that contained hyperechoic areas.
34 rmine the relationship of testicular cancer,
intratesticular mass, and microlithiasis.
35 Ninety patients had an
intratesticular mass, of whom 23 (26%) had microlithiasi
36 Seventeen
intratesticular masses and one extratesticular mass were
37 All
intratesticular masses contained vascular structures tha
38 th US findings suggestive of microlithiasis,
intratesticular masses, and intratesticular heterogeneou
39 ve value of 94.7% in the characterization of
intratesticular masses.
40 stis was found in the center of 11 of the 17
intratesticular masses.
41 noprivileged organ, and at 37 degrees C, the
intratesticular microenvironment supports the survival o
42 Intratesticular microlithiasis is highly associated with
43 call for more effective means of inhibiting
intratesticular T production or action, to achieve consi
44 nthesis, and 17-OH-progesterone, a marker of
intratesticular T, were also enriched in the dorsal vein
45 lso negatively correlated (R(2) = -0.5) with
intratesticular testosterone (ITT) at e21.5, but only wh
46 In rats, fetal LC size and
intratesticular testosterone (ITT) increased ~3-fold bet
47 ibutyl phthalate (DBP) -induced reduction in
intratesticular testosterone in rats reduced ALC stem ce
48 ele and varicocelectomy to assess changes in
intratesticular testosterone levels.
49 ale offspring, resulting from suppression of
intratesticular testosterone, and is used as a model for
50 tosterone production and drastically reduces
intratesticular testosterone, consequently impairing spe
51 oth pathways produced normal basal levels of
intratesticular testosterone, suggesting the action of o
52 Newly described conditions such as
intratesticular varicoceles and other benign intratestic
53 Power Doppler US improves depiction of
intratesticular vessels, but flow cannot be identified i