about
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromesNovel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvementRole of miR-27a, miR-181a and miR-20b in gastric cancer hypoxia-induced chemoresistance.Nuclear PARP1 expression and its prognostic significance in breast cancer patients.β-catenin interaction with NHERF1 and RASSF1A methylation in metastatic colorectal cancer patientsSister chromatid exchange: A possible approach to characterize familial breast cancer patients
P50
Q24625476-451CE383-096F-4DF0-919E-AC0BF35451E7Q34054602-E3F19994-43CE-4E4C-B74D-537A71EA37B9Q34896062-EE3DF38E-912F-4BD0-B7B4-2BCE034660D8Q37013255-6C16C91F-4A5E-46A7-A79B-F5A098D41907Q41091405-209FB420-EA90-422A-B275-D47E6BEC4B57Q42315542-8F301461-8F91-448A-87D3-0A96D47653F3Q86080582-0F4CDF00-3974-4778-8128-097308202BD9
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Annalisa Mazzotta
@ast
Annalisa Mazzotta
@en
Annalisa Mazzotta
@es
Annalisa Mazzotta
@nl
type
label
Annalisa Mazzotta
@ast
Annalisa Mazzotta
@en
Annalisa Mazzotta
@es
Annalisa Mazzotta
@nl
prefLabel
Annalisa Mazzotta
@ast
Annalisa Mazzotta
@en
Annalisa Mazzotta
@es
Annalisa Mazzotta
@nl
P106
P1153
26431058700
P31
P496
0000-0002-1937-9765