ライフサイエンスコーパス: skeletal malformation

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1 to abnormal somite differentiation and axial skeletal malformation.

2 and its application to the classification of skeletal malformations.

3 sents with disordered sexual development and skeletal malformations.

4 h multiple systemic abnormalities, including skeletal malformations.

5 morphia, short stature, cardiac defects, and skeletal malformations.

6 a mechanistic basis for most of the observed skeletal malformations.

7 COX-2 transgenic fetuses exhibit severe skeletal malformations and die shortly after birth.

8 or this mutation die at birth as a result of skeletal malformations and neural tube defects.

9 OP) is a rare autosomal dominant disorder of skeletal malformations and progressive extraskeletal oss

10 terized by autosomal XY sex reversal, severe skeletal malformations and several craniofacial defects.

11 owth retardation, obesity, blepharophimosis, skeletal malformation, and increased serum lipid metabol

12 Skeletal malformations are localized along the entire ve

13 Klippel-Feil syndrome is a skeletal malformation characterized by vertebral fusion.

14 s in increased chondrocyte proliferation and skeletal malformations consistent with the observed incr

15 Although the skeletal malformations did not phenocopy single or compo

16 increase in both occurrence and severity of skeletal malformations, extending from the craniocervica

17 shown to cause idiopathic short stature and skeletal malformations frequently observed in human pati

18 We show that the apoptosis and consequent skeletal malformations in acd mutants are dependent upon

19 gests that Cx40 deficiency accounts for many skeletal malformations in HOS and that Tbx5 regulation o

20 h mutations in FGF signaling molecules cause skeletal malformations in humans.

21 esponsible for the gametogenesis defects and skeletal malformations in the sks mice.

22 apoptosis is probably responsible for axial skeletal malformations in transgenic fetuses.

23 are reminiscent of the dominantly inherited skeletal malformation nail patella syndrome (NPS).

24 human motor neuropathies, arthropathies, and skeletal malformations of varying severity.

25 X9 gene cause campomelic dysplasia, a severe skeletal malformation syndrome associated with male-to-f

26 Campomelic dysplasia (CD) is a semilethal skeletal malformation syndrome with or without XY sex re

27 patients with campomelic dysplasia, a severe skeletal malformation syndrome, and the abundant express

28 cy results in campomelic dysplasia, a lethal skeletal malformation syndrome, and XY sex reversal.

29 (NICD) in the chondrocyte lineage results in skeletal malformations with decreased cartilage precurso

30 The mutants also have skeletal malformations with fused vertebrae and ribs.

31 ion component, shared axial and appendicular skeletal malformations with Tbx5(+/Delta) mice.

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