ライフサイエンスコーパス: volar

1 histologic subtype (P = 0.05) compared with volar acral melanomas.

2 Lesions in the volar and dorsal radioulnar ligament and lesions of the

3 most notably of rare melanomas that occur on volar and mucosal surfaces of the skin.

4 n a limited sample size, differences between volar and subungual/interdigital melanomas in our study

5 demonstrated clear differences compared with volar and subungual/interdigital melanomas.

6 easured constitutive skin color at the upper volar arm fit a quadratic equation (r(2)=0.94) that diff

7 ment of constitutive skin color at the upper volar arm provides a quick, noninvasive, precise, and ac

8 lity of constitutive skin color at the upper volar arm was 3 and 5% coefficient of variation (CV), re

9 Constitutive skin color at the upper volar arm was equal to the buttocks.

10 e transverse carpal ligament (TCL) forms the volar boundary of the carpal tunnel and may provide mech

11 The volar donor sites were well-tolerated, healed rapidly, a

12 The transcriptional signature of the volar-enriched subpopulation is retained in acral melano

13 transcriptome of in vivo palmoplantar (i.e., volar) epidermis is globally unique, including Keratin 9

14 t to the CLs were more common than dorsal or volar erosions.

15 lar fibroblasts into nonvolar skin increased volar features that lasted up to 5 months, highlighting

16 Although volar fibroblasts have the capacity to induce KRT9 in no

17 nocyte differentiation, we hypothesized that volar fibroblasts influence these features.

18 althy volunteers demonstrated that injecting volar fibroblasts into nonvolar skin increased volar fea

19 ed skin constructs confirmed the capacity of volar fibroblasts to induce volar keratinocyte features.

20 of ectopic expression of KRT9 independent of volar fibroblasts, we demonstrate that in the human skin

21 KRT9 expression is selectively activated by volar fibroblasts.

22 scussed: fluoroquinolone-induced tendinitis, volar flexor tenosynovitis (trigger finger), Achilles te

23 Volar flexor tenosynovitis and trigger finger are among

24 /GP1908/2015 H1N1 HA antigen (A-Sing) to the volar forearm (FA); uncoated HD-MAPs; intramuscular (IM)

25 en for at least 4 hours (preprandial) on one volar forearm and 60 minutes after a carbohydrate-rich m

26 extremely low-biomass skin sites such as the volar forearm and antecubital fossa.

27 ented on the selective early weakness of the volar forearm muscles, quadriceps, and ankle dorsiflexor

28 that BAM8-22 evokes in humans, we tested the volar forearm of 15 healthy volunteers with heat-inactiv

29 Sites on the volar forearm of humans were exposed to photomechanical

30 ed up to 21 skin tape strips (STSs) from the volar forearm of non-AD subjects with EoE (n = 21) and n

31 enylalanine (Phe) and tyrosine (Tyr), on the volar forearm of six healthy volunteers.

32 ainful heat stimuli were applied to the left volar forearm while different color shapes explicitly si

33 whole-metagenome profiling at 4 body sites (volar forearm, antecubital fossae, cheeks, and lesions)

34 ons on various parts of the body such as the volar forearm, forehead, cheeks, and hands.

35 cted stratum corneum (SC) specimens from the volar forearms of 10 CSU patients, 10 AD patients, and 1

36 ding a polydimethylsiloxane ball against the volar forearms to simulate the skin-PPE interface.

37 Eleven of 12 neurons with tactile RFs on the volar forepaw began firing toward the end of swing, with

38 the capacity of volar fibroblasts to induce volar keratinocyte features.

39 Despite this, KRT9 expression is lost with volar keratinocyte passaging, despite stable hypomethyla

40 in nonvolar keratinocytes, we show here that volar keratinocytes continue to express KRT9 in in vitro

41 NA inhibits KRT9 expression in early passage volar keratinocytes or in vivo footpads of wild-type mic

42 Loss of DDX58 in passaged volar keratinocytes rescues KRT9 and inhibits KRT7 expre

43 Keratin 9 is highly enriched in volar keratinocytes, and its expression is dependent on

44 t robustly expressed gene in differentiating volar keratinocytes, is markedly downregulated in Krt16-

45 rsity of the skin biota from the superficial volar left and right forearms in six healthy subjects us

46 g, open reduction and internal fixation with volar lock plating (ORIF), external fixation, percutaneo

47 o selected surgery were randomly assigned to volar lock plating, percutaneous pinning, or external fi

48 ipants were randomized to open reduction and volar locking plate system (VLPS), external fixation wit

49 open reduction and internal fixation using a volar-locking plate (VLP group) and nonsurgical treatmen

50 open reduction and internal fixation using a volar-locking plate (VLP).

51 The volar, middle, and dorsal portions of the SLL can be dif

52 Coronal 3D GRE imaging was used to study the volar, middle, and dorsal portions of the SLL in 14 pati

53 ssed melanomas occurring on dorsal (n = 21), volar (n = 9), and subungual/interdigital (n = 13) acral

54 wth of the basal layer and regression of the volar pads during the time of ridge formation.

55 ore dense in the distal than in the proximal volar pads.

56 t for evaluation of persistent pain over the volar portion of his right fifth finger after a fall dur

57 The trapezoidal volar portion of the SLL was seen with inhomogeneous hig

58 a and KRT9 are robustly activated outside of volar sites.

59 collagen length, and elastin are markers of volar skin and likely contribute to volar skin resilienc

60 en the critical functional importance of the volar skin areas.

61 n autologous donor volar skin tissue, confer volar skin characteristics ectopically to nonvolar skin

62 structural and molecular characteristics of volar skin ectopically to other skin areas.

63 arring, which are especially problematic for volar skin given the critical functional importance of t

64 Transplanting volar skin onto amputation stumps could be a solution to

65 rkers of volar skin and likely contribute to volar skin resiliency.

66 ractical approach to obtain autologous donor volar skin tissue, confer volar skin characteristics ect

67 lity of fibroblasts to reprogram nonvolar to volar skin to reduce stump dermatoses in patients with l

68 ed skin covering the palms and soles (a.k.a. volar skin).

69 is the most uniquely enriched transcript in volar skin, consistent with its etiology in genetic dise

70 the site-specific epidermal cell identity on volar skin.

71 mputees to pressure-responsive palmoplantar (volar) skin to enhance prosthesis use and minimize skin

72 eks, and tissue samples were taken to verify volar-specific characteristics by histology and immunohi

73 The graft sites were able to maintain volar-specific histologic features and expression of cha

74 He also had a small nodule on the volar surface of his right ring finger.

75 ons in the peripheral nerves innervating the volar surface of the hand.

76 p2(-/-) mice exhibited hyperkeratosis on the volar surface of the paws (i.e., palmoplantar keratoderm

77 veform derived from the radial artery at the volar surface of the wrist.

78 ized the gene expression differences between volar (ventral; palmoplantar) and nonvolar (dorsal) huma

79 hognomonic burrows on finger/toe web spaces, volar wrists, ankles, axillae, buttocks, male genitalia,