Detalhe da pesquisa
1.
A finely tuned interplay between calcium binding, ionic strength and pH modulates conformational and oligomerization equilibria in the Respiratory Syncytial Virus Matrix (M) protein.
Arch Biochem Biophys
; 731: 109424, 2022 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36220378
2.
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Nat Genet
; 23(3): 319-22, 1999 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-10545950
3.
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation.
J Med Genet
; 45(7): 447-50, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18456720
4.
Palatal asymmetry during development: an anatomical study.
Clin Anat
; 21(5): 398-404, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18521940
5.
Development of synovial membrane in the temporomandibular joint of the human fetus.
Eur J Histochem
; 59(4): 2569, 2015 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26708184
6.
Expressions of E2 and E7-HPV16 proteins in pre-malignant and malignant lesions of the uterine cervix.
Biotech Histochem
; 90(8): 573-80, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26052817
7.
Folding of a dimeric beta-barrel: residual structure in the urea denatured state of the human papillomavirus E2 DNA binding domain.
Protein Sci
; 9(4): 799-811, 2000 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-10794423
8.
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes.
Hum Mutat
; 16(4): 315-22, 2000 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11013442
9.
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia.
Am J Med Genet
; 95(5): 482-91, 2000 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-11146471
10.
Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.
Am J Med Genet
; 78(3): 237-41, 1998 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-9677057
11.
Immunohistochemical expression of types I and III collagen antibodies in the temporomandibular joint disc of human foetuses.
Eur J Histochem
; 55(3): e24, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22073371
12.
Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1-->qter duplication.
J Med Genet
; 38(1): 73-6, 2001 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11334012
13.
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.
Clin Genet
; 67(6): 503-10, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15857417
14.
Clinical spectrum of fibroblast growth factor receptor mutations.
Hum Mutat
; 14(2): 115-25, 1999.
Artigo
em Inglês
| MEDLINE | ID: mdl-10425034
15.
Neutrophil antigen 5b is carried by a protein, migrating from 70 to 95 kDa, and may be involved in neonatal alloimmune neutropenia.
Transfusion
; 40(2): 222-7, 2000 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10686007
16.
Distinctive cognate sequence discrimination, bound DNA conformation, and binding modes in the E2 C-terminal domains from prototype human and bovine papillomaviruses.
Biochemistry
; 39(47): 14692-701, 2000 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-11087426