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1 elphys with blind hemivagina and ipsilateral renal agenesis.
2 ephric mesenchyme is inhibited, resulting in renal agenesis.
3 a densa of the basement membrane and also in renal agenesis.
4 line-derived neurotrophic factor results in renal agenesis.
5 lphys, obstructed hemivagina and ipsilateral renal agenesis.
6 de (classification 1.2) with associated left renal agenesis.
7 orn fetuses that had bilateral or unilateral renal agenesis (29 subjects) or severe congenital renal
8 were found in 7 of 19 fetuses with bilateral renal agenesis (37%) and 2 of 10 fetuses (20%) with unil
9 s for understanding how this mutation caused renal agenesis, a failure of fetal kidney development.
11 eads to failure of mesenchymal induction and renal agenesis, an early developmental phenotype that pr
12 in the neonatal period, exhibiting bilateral renal agenesis and defects of the eye and the skeleton.
15 reased incidence of unilateral and bilateral renal agenesis, and smaller kidneys with fewer nephrons.
17 (Obstructed Seminal Vesicle and Ipsilateral Renal Agenesis) as an acronym for Zinner syndrome analog
18 ects than sall1-null mice including complete renal agenesis, exencephaly, limb and anal deformities.
19 ocal translocation associated with bilateral renal agenesis has implicated the gene encoding the nucl
20 erogeneous stock-derived model of unilateral renal agenesis (HSRA) rat, which demonstrates 50%-75% sp
21 alies included duplex and multiplex kidneys, renal agenesis, hydronephrosis and cystic kidney disease
22 of temperature indicators were observed for renal agenesis/hypoplasia (positive) and anophthalmia/mi
23 ng nephrogenesis, the demonstrated rescue of renal agenesis in a model of a human genetic disease rai
25 ssed by the ureteric bud, leads to bilateral renal agenesis in humans with Fraser syndrome and blebbe
26 auses CAKUT that are markedly different than renal agenesis in Ret-null or RetY1062F mutant mice.
27 ble, Gfralpha1(TM/TM) mice display bilateral renal agenesis, lack enteric neurons in the intestines,
28 h the specific CAKUT phenotype of unilateral renal agenesis may also be mutated in humans with isolat
29 e phenotypes of intestinal aganglionosis and renal agenesis observed in homozygous RET knockout (Ret
30 in the branching ureteric bud (UB), and that renal agenesis occurs in homozygous Fras1 null mutant bl
31 of the most severe renal anomaly, bilateral renal agenesis or hypoplasia (RA/H), has limited the abi
33 62)-mediated AKT/MAPK activation resulted in renal agenesis or kidney rudiments, whereas mutation of
35 sized that stillborn fetuses with congenital renal agenesis or severe dysplasia would possess mutatio
36 homozygous for a mutation in c-ret displayed renal agenesis or severe hypodysplasia, suggesting a cri
37 Etv4 alleles and one Etv5 allele show either renal agenesis or severe hypodysplasia, whereas kidney d
38 of the GAG chain is key as evidenced by the renal agenesis phenotype in mice deficient in the HS bio
39 evailing view that the defect underlying the renal agenesis phenotype is due to a primary role for 2-
40 mation of subepidermal hemorrhagic blisters, renal agenesis, syndactyly or polydactyly and permanent
41 shown that a loss of Eya 1 function leads to renal agenesis that is a likely result of failure of met
42 ranging from severe manifestations, such as renal agenesis, to potentially milder conditions, such a
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