ライフサイエンスコーパス: anlagen

1 d during development of the new macronuclei (anlagen).

2 ns and outgrowth of the embryonic endodermal anlagen.

3 lonization of, and/or fiber assembly in, the anlagen.

4 ercular muscles derived from the same muscle anlagen.

5 e linked to defective formation of cartilage anlagen.

6 nction that patterns the proximal pronephric anlagen.

7 the dorso-anterior region of the pronephros anlagen.

8 remodel the primary, cartilaginous skeletal anlagen.

9 precursors prior to reaching the sympathetic anlagen.

10 in contrast to the other chondrocytes of the anlagen.

11 Pitx2 mutant mice form all but a few muscle anlagen.

12 s derived from the early chondrocytes of the anlagen.

13 d RUNX2, during condensation of the skeletal anlagen.

14 enitor cells in the CNC-derived frontal bone anlagen.

15 other tissues surrounding the cranial muscle anlagen.

16 e mesenchyma in lymph node and Peyer's patch anlagen.

17 es situated near the distal ends of skeletal anlagen.

18 both the red nucleus and oculomotor complex anlagen.

19 ncluding differentiation of new macronuclear anlagen.

20 the neocortex and aplasia of the hippocampal anlagen.

21 lead to an abnormal specification of the eye anlagen.

22 f postzygotic gene expression, presumably in anlagen.

23 epiphyseal region of mouse embryo long bone anlagen - a region encompassing the groove of Ranvier -

24 ling patterns the early X. laevis pronephros anlagen, a function that might be conserved in mammalian

25 g PP development, where they aggregate at PP anlagen after stromal cell activation and become a local

26 Transplants of Ihh-null anlagen also developed normally.

27 germinal matrix relative to the white matter anlagen and cortical mantle.

28 in the subarticular regions of the cartilage anlagen and entheses at a time point most relevant to th

29 ion in Meckel's cartilage and the mandibular anlagen and for the formation of the coronoid, condyle a

30 inding partners in both dissected pronephric anlagen and in individual dissected components of stage

31 d role in early axial patterning of the germ anlagen and in the specification of gnathal and thoracic

32 the myogenic progression in embryonic muscle anlagen and persists in adult muscle.

33 b skeletogenesis the cartilaginous long bone anlagen and their growth plates become delimited by peri

34 left/right integration into the future adult anlagen appears to be controlled by a late developmental

35 Mammary anlagen are formed in the embryo as a derivative of the

36 nsport of the phytohormone auxin with floral anlagen arising at sites of auxin maxima.

37 lonizes pre-patterned regions to form muscle anlagen as muscle fibers are assembled.

38 ow that FoxM1 is expressed in the cerebellar anlagen as well as in postnatal proliferating CGNP and t

39 appear to be expressed throughout primordia anlagen before becoming confined to their corresponding

40 y the progressive replacement of a cartilage anlagen by bone at the growth plate with a tight balance

41 t of organogenesis, as colonization of organ anlagen by pMacs is followed by their specification into

42 earrangements in the developing macronuclei (anlagen) causes aberrant anlage DNA loss, suggesting tha

43 Loss or degeneration in muscle anlagen could generally be attributed to the loss of a m

44 muscle precursors (myotomes), limb skeletal anlagen, craniofacial regions, and nephric ducts.

45 essed in the embryo and in initiating floral anlagen, demonstrating a specific role for PID in promot

46 Remarkably, pancreatic anlagen derived from pDKO embryos also display a dramati

47 rough mating but arrest at late macronuclear anlagen development and die before the first post-conjug

48 active throughout the GI and in the nephros anlagen during development, we find that Rb inactivation

49 ules and is expressed in the gut and nephros anlagen during embryogenesis.

50 ion in Hh-responsive cells of the wing blade anlagen during the late third instar creates a zone of c

51 s include general core histones and a second anlagen-enriched polypeptide (Pdd2p, formerly known as p

52 ed to Hdh-Q18 embryos, the Hdh-Q111 striatal anlagen exhibited significantly higher levels of the ess

53 when HS function was disrupted in long bone anlagen explants by genetic, pharmacological or enzymati

54 ing tubulogenesis, the developing pronephric anlagen expresses Daam1 and its interacting Rho-GEF (WGE

55 mainder of the chondrocytes in the cartilage anlagen expresses matrilin-1.

56 gnals from the PZ maintain the AER until the anlagen for the distal phalanges have been formed.

57 ring meiosis for the micronucleus and during anlagen formation for the macronucleus.

58 The fibrous sheath anlagen formed, but the definitive fibrous sheath did no

59 te that the corona initiates as six separate anlagen from hypanthial tissue between the stamens and p

60 y be a common theme for the budding of organ anlagen from the endoderm.

61 In the early larva, the optic anlagen grow as epithelia by symmetric cell division.

62 individual tissue specificities in the digit anlagen, growth plates, skull sutures and fingertips.

63 strong hoxc-4 expression in the prevertebral anlagen (i.e., pv7-14).

64 development begins, ftILCPs accumulate at PP anlagen in a lymphotoxin-alpha-dependent manner.

65 developmental identities of the avian digit anlagen in later ontogeny such that CII becomes DI, CIII

66 st Ro 41-5253 or AGN 193109 near the humeral anlagens in stage 21 (Day 3.5) or stage 27 chick embryos

67 na, is found only in developing macronuclei (anlagen) in association with chromatin containing the se

68 d by proximal elongation of the wrist tendon anlagen, in parallel with skeletal growth, underscoring

69 ryogenesis, we transplanted Shh-null mammary anlagen into cleared fat pads and under the renal capsul

70 erning remodeling of unmineralized cartilage anlagen into membranous bone, as well as tendons and lig

71 lethality, we transplanted pRb-null mammary anlagen into wild hosts.

72 Cell proliferation within the optic lobe anlagen is dependent on ecdysteroids during metamorphosi

73 veloping cartilaginous and ossified skeletal anlagen is encapsulated within a membranous sheath of fl

74 expression of several genes in the early eye anlagen is required for the dorsoventral (DV) and antero

75 erm, we report that, in fact, two pancreatic anlagen join to form the pancreas.

76 soul mutant embryos, in which the pancreatic anlagen most often do not fuse, we show that the posteri

77 ividual organ anlagen, whereas the digestive anlagen of amniotes arise from a primitive gut tube.

78 The cartilage anlagen of axial skeleton fail to properly develop in tr

79 ome and later around the vertebral cartilage anlagen of body and pedicles.

80 ery short zeugopod and connect through short anlagen of tendon progenitors at the presumptive wrist t

81 Other genes mark the anlagen of the cardiac and somatic mesoderm and these ar

82 e midgut, and serpent (srp), which marks the anlagen of the fat body.

83 The otic placode, the anlagen of the inner ear, develops from an ectodermal fi

84 ttery of molecular markers, we show that the anlagen of the inner ear, the otic placode, is induced i

85 midline' in the following) that includes the anlagen of the medial brain, the visual system (optic lo

86 association with the muscle remnants and the anlagen of the new adult muscles.

87 When isolated at E13.5, the anlagen of the SCN expresses high, arrhythmic PER2.

88 rmal genes: bagpipe (bap), which defines the anlagen of the visceral musculature of the midgut, and s

89 ateral axis of the dorso-anterior pronephros anlagen, permitting the glomus and tubules to develop in

90 ilar to other epithelial appendages, mammary anlagen progress from stratified epithelium through plac

91 utative signal transduction receptor, ASI2, (anlagen stage induced 2) is up-regulated during developm

92 distortion, rather than loss, of limb muscle anlagen, suggesting that its function becomes critical d

93 n domains correspond to two or three segment anlagen that fail to develop in each mutant.

94 ing an accumulation pattern in the mouthpart anlagen that is conserved across several insect orders.

95 were occasionally observed in the prostatic anlagen, the urogenital sinus (UGS) of FGF-10(-/-) mice.

96 Mullerian duct or female reproductive tract anlagen; this event is essential for proper male sexual

97 Wnt-4 then patterns the proximal pronephric anlagen to establish the specific compartments that span

98 e organization, migration of hypaxial muscle anlagen toward the ventral abdomen, and development of j

99 Limb long bone anlagen were entirely composed of chondrocytes actively

100 the chondrocytes of all developing cartilage anlagen, where it essential during initial growth and pa

101 ve system is assembled from individual organ anlagen, whereas the digestive anlagen of amniotes arise

102 mandibular condyle that generates cartilage anlagen, which is subsequently remodeled into vasculariz

103 , are expressed in the epithelial optic lobe anlagen, which matches the widespread epithelial express

104 The latter proceeds via cartilage anlagen, which through hypertrophy, mineralization, and