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HOXA5-twist interaction alters p53 homeostasis in breast cancer cellsA 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactylyLimb malformations and the human HOX genesA survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individualsGermline mutations in HOXB13 and prostate-cancer riskSometimes the result is not the answer: the truths and the lies that come from using the complementation testMesenchymal-epithelial interactions during digestive tract development and epithelial stem cell regenerationA HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth diseaseMolecular genetics of Müllerian duct formation, regression and differentiationFunctional classification and mutation analysis of a synpolydactyly kindred.Stability of proposed biomarkers of prenatal androgen exposure over the menstrual cycle.HOXB13 and ALX4 induce SLUG expression for the promotion of EMT and cell invasion in ovarian cancer cells.Homeodomain revisited: a lesson from disease-causing mutations.HOXB13 mutations in a population-based, case-control study of prostate cancer.HOXB13 mutation and prostate cancer: studies of siblings and aggressive diseaseAn increased duplication of ZRS region that caused more than one supernumerary digits preaxial polydactyly in a large Chinese family.Folate modulates Hox gene-controlled skeletal phenotypes.Translating genetic risk factors for prostate cancer to the clinic: 2013 and beyond.Tail gut endoderm and gut/genitourinary/tail development: a new tissue-specific role for Hoxa13.Bilateral proximal delta phalanges: an unusual presentation of familial congenital clinodactyly.Genome-wide association analyses identify variants in developmental genes associated with hypospadias.Homeobox gene expression and mutation in cervical carcinoma cells.Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus.Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster.Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update.
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Human HOX gene mutations
@ast
Human HOX gene mutations
@en
Human HOX gene mutations
@nl
type
label
Human HOX gene mutations
@ast
Human HOX gene mutations
@en
Human HOX gene mutations
@nl
prefLabel
Human HOX gene mutations
@ast
Human HOX gene mutations
@en
Human HOX gene mutations
@nl
P2860
P1433
P1476
Human HOX gene mutations
@en
P2093
F R Goodman
P J Scambler
P2860
P356
10.1034/J.1399-0004.2001.590101.X
P407
P577
2001-01-01T00:00:00Z