Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
about
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndromeLoss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneityHamartomatous polyposis syndromesMolecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancerGenodermatosesA novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.Population-based estimate of sibling risk for preterm birth, preterm premature rupture of membranes, placental abruption and pre-eclampsia.Mutations in STK11 gene in Czech Peutz-Jeghers patientsHereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes.A gene for familial juvenile polyposis maps to chromosome 18q21.1.E2A-HLF usurps control of evolutionarily conserved survival pathways.Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndromeMutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.Correlation of staining for LKB1 and COX-2 in hamartomatous polyps and carcinomas from patients with Peutz-Jeghers syndrome.Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndromeSTRAD in Peutz-Jeghers syndrome and sporadic cancers.Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.From developmental disorder to heritable cancer: it's all in the BMP/TGF-beta family.Cancer risks in LKB1 germline mutation carriers.[Peutz-Jeghers syndrome, about 3 cases in siblings].The hamartomatous polyposis syndromes: a clinical and molecular review.Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.Hepatic mesenchymal hamartoma: cytogenetic analysis of a case and review of the literature.Correlation between genotype and phenotype in three families with Peutz-Jeghers Syndrome.LKB1 as a Tumor Suppressor in Uterine Cancer: Mouse Models and Translational Studies.Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome.STK11 status and intussusception risk in Peutz-Jeghers syndrome.Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.Familial Adenomatous Polyposis (FAP) and Other Polyposis Syndromes.Exome sequencing revealed novel germline mutations in Chinese Peutz-Jeghers syndrome patients.
P2860
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P2860
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
name
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@ast
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@en
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@nl
type
label
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@ast
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@en
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@nl
prefLabel
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@ast
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@en
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@nl
P2093
P2860
P356
P1476
Peutz-Jeghers syndrome: confir ...... tial second locus, on 19q13.4.
@en
P2093
Bermejo-Fenoll A
Bhardwaj K
Bhardwaj SS
Radhakrishna U
Richards KF
P2860
P304
P356
10.1086/301644
P407
P577
1997-12-01T00:00:00Z