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1.
Braz Oral Res ; 33: e058, 2019 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-31432925

RESUMEN

Cementum is the mineralized tissue covering the tooth root that functions in tooth attachment and post-eruptive adjustment of tooth position. It has been reported to be highly similar to bone in several respects but remains poorly understood in terms of development and regeneration. Here, we investigate whether cementocytes, the residing cells in cellular cementum, have the potential to be protagonist in cementum homeostasis, responding to endocrine signals and directing local cementum metabolism. Cells from healthy erupted human teeth were isolated using sequential collagenase/EDTA digestions, and maintained in standard cell culture conditions. A cementocyte-like cell line was cloned (HCY-23, for human cementocyte clone 23), which presented a cementocyte compatible gene expression signature, including the expression of dentin matrix protein 1 ( DMP1 ), sclerostin ( SOST ), and E11/gp38/podoplanin ( E11 ). In contrast, these cells did not express the odontoblast/dentin marker dentin sialoprotein ( DSPP ). HCY-23 cells produced mineral-like nodules in vitro under differentiation conditions, and were highly responsive to inorganic phosphate (Pi). Within the limits of the present study, it can be concluded that cementocytes are phosphate-responsive cells, and have the potential do play a key role in periodontal homeostasis and regeneration.


Asunto(s)
Técnicas de Cultivo de Célula/métodos , Cemento Dental/citología , Proteínas Adaptadoras Transductoras de Señales , Adolescente , Adulto , Análisis de Varianza , Proteínas Morfogenéticas Óseas/análisis , Proteínas Morfogenéticas Óseas/genética , Línea Celular , Cemento Dental/metabolismo , Proteínas de la Matriz Extracelular/análisis , Proteínas de la Matriz Extracelular/genética , Femenino , Técnica del Anticuerpo Fluorescente , Expresión Génica , Marcadores Genéticos/genética , Humanos , Masculino , Glicoproteínas de Membrana/análisis , Glicoproteínas de Membrana/genética , Diente Molar/citología , Fosfatos/farmacología , Fosfoproteínas/análisis , Fosfoproteínas/genética , Sialoglicoproteínas/análisis , Sialoglicoproteínas/genética , Factores de Tiempo , Adulto Joven
2.
Braz. oral res. (Online) ; 33: e058, 2019. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1019608

RESUMEN

Abstract Cementum is the mineralized tissue covering the tooth root that functions in tooth attachment and post-eruptive adjustment of tooth position. It has been reported to be highly similar to bone in several respects but remains poorly understood in terms of development and regeneration. Here, we investigate whether cementocytes, the residing cells in cellular cementum, have the potential to be protagonist in cementum homeostasis, responding to endocrine signals and directing local cementum metabolism. Cells from healthy erupted human teeth were isolated using sequential collagenase/EDTA digestions, and maintained in standard cell culture conditions. A cementocyte-like cell line was cloned (HCY-23, for human cementocyte clone 23), which presented a cementocyte compatible gene expression signature, including the expression of dentin matrix protein 1 ( DMP1 ), sclerostin ( SOST ), and E11/gp38/podoplanin ( E11 ). In contrast, these cells did not express the odontoblast/dentin marker dentin sialoprotein ( DSPP ). HCY-23 cells produced mineral-like nodules in vitro under differentiation conditions, and were highly responsive to inorganic phosphate (Pi). Within the limits of the present study, it can be concluded that cementocytes are phosphate-responsive cells, and have the potential do play a key role in periodontal homeostasis and regeneration.


Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Adulto Joven , Marcadores Genéticos/genética , Técnicas de Cultivo de Célula/métodos , Cemento Dental/citología , Fosfatos/farmacología , Fosfoproteínas/análisis , Fosfoproteínas/genética , Sialoglicoproteínas/análisis , Sialoglicoproteínas/genética , Factores de Tiempo , Glicoproteínas de Membrana/análisis , Glicoproteínas de Membrana/genética , Expresión Génica , Línea Celular , Análisis de Varianza , Proteínas de la Matriz Extracelular/análisis , Proteínas de la Matriz Extracelular/genética , Técnica del Anticuerpo Fluorescente , Proteínas Morfogenéticas Óseas/análisis , Proteínas Morfogenéticas Óseas/genética , Cemento Dental/metabolismo , Proteínas Adaptadoras Transductoras de Señales , Diente Molar/citología
3.
Sex Transm Dis ; 44(1): 35-41, 2017 01.
Artículo en Inglés | MEDLINE | ID: mdl-27898568

RESUMEN

BACKGROUND: Ideal management of sexually transmitted infections (STI) may require risk markers for pathology or vaccine development. Previously, we identified common genetic variants associated with chlamydial pelvic inflammatory disease (PID) and reduced fecundity. As this explains only a proportion of the long-term morbidity risk, we used whole-exome sequencing to identify biological pathways that may be associated with STI-related infertility. METHODS: We obtained stored DNA from 43 non-Hispanic black women with PID from the PID Evaluation and Clinical Health Study. Infertility was assessed at a mean of 84 months. Principal component analysis revealed no population stratification. Potential covariates did not significantly differ between groups. Sequencing kernel association test was used to examine associations between aggregates of variants on a single gene and infertility. The results from the sequencing kernel association test were used to choose "focus genes" (P < 0.01; n = 150) for subsequent Ingenuity Pathway Analysis to identify "gene sets" that are enriched in biologically relevant pathways. RESULTS: Pathway analysis revealed that focus genes were enriched in canonical pathways including, IL-1 signaling, P2Y purinergic receptor signaling, and bone morphogenic protein signaling. CONCLUSIONS: Focus genes were enriched in pathways that impact innate and adaptive immunity, protein kinase A activity, cellular growth, and DNA repair. These may alter host resistance or immunopathology after infection. Targeted sequencing of biological pathways identified in this study may provide insight into STI-related infertility.


Asunto(s)
Infecciones por Chlamydia/genética , Secuenciación del Exoma , Infertilidad/genética , Enfermedad Inflamatoria Pélvica/genética , Transducción de Señal/genética , Adulto , Proteínas Morfogenéticas Óseas/análisis , Infecciones por Chlamydia/complicaciones , Femenino , Humanos , Infertilidad/microbiología , Interleucina-1/análisis , Enfermedad Inflamatoria Pélvica/complicaciones , Enfermedad Inflamatoria Pélvica/microbiología , Análisis de Componente Principal , Receptores Purinérgicos P2Y/análisis
4.
Pesqui. vet. bras ; Pesqui. vet. bras;34(supl.1): 92-98, dez. 2014. ilus
Artículo en Portugués | LILACS, VETINDEX | ID: lil-778361

RESUMEN

O desenvolvimento embrionário dos peixes é de grande importância para a piscicultura e na reintrodução de espécies ameaçadas de extinção em seus ambientes, e seu conhecimento constitui uma importante maneira para minimizar doenças e mortalidades dessas espécies. Com o auxílio de técnicas como a Microscopia Eletrônica de Varredura (MEV) e a imuno-histoquimica para identificar proteínas ósseas, foi possível avaliar as fases de desenvolvimento com mais riqueza de detalhes, facilitando a compreensão de hábitos e da biologia da espécie. Neste trabalho pudemos observar a ontogenia e osteogênese da Piapara (Leporinus elongatus), desde a fecundação até a fase juvenil, sendo evidenciadas estruturas importantes como o tamanho do vitelo, essencial para a nutrição do embrião; o fechamento do blastóporo, evento principal da embriogênese, que indica as taxas de fertilização; a metamorfose, que indica a formação dos primeiros e principais órgãos do animal e a formação de sua estrutura óssea. As Proteínas Ósseas Morfogenéticas (BMP-2 e BMP-4), moléculas essenciais reguladoras no desenvolvimento embrionário e na formação óssea, foram observadas apenas no estádio larval até o período juvenil, não sendo evidenciadas nos estágios anteriores. Os resultados desse trabalho trouxeram novas informações quanto à biologia do desenvolvimento dessa espécie, que certamente poderão auxiliar no aprimoramento de técnicas reprodutivas visando uma melhora na sua produção seja para fins comerciais ou de repovoamento.(AU)


The embryonic development of fishes has great importance in fish culture and on reintroduction of species at risk of extinction into their environment; its knowledge constitutes an important way to minimize diseases and mortality of these species. By using techniques like electron microscopy and immunohistochemistry for bone markers identification, it was possible to evaluate the developmental stages of Leporinus elongatus in more details, helping to clarify the habits and biology of this species. Results showed the ontogeny and ostheogenesis of of Leporinus elongatus this species from fecundation to juvenile, evidencing important structures as size of the yolk, essential to embryo nutrition, the blastopores closure, important event in embryogenesis because it indicates fertilization indexes, and the metamorphosis, which shows the main organs' development including bones. Bone morphogenetic markers 1 and 4, essential regulatory molecules for bone development, had their expression restricted from larva to fry stages, and were not observed in their previous stages. In sum, these results provided new data that may improve reproductive techniques for L. elongatus, and will support commercial and repopulation purposes.(AU)


Asunto(s)
Animales , Osteogénesis/fisiología , Proteínas Morfogenéticas Óseas/análisis , Desarrollo Embrionario/fisiología , Characiformes/embriología , Inmunohistoquímica
5.
J Clin Periodontol ; 41(6): 550-7, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24576302

RESUMEN

AIM: The regulation of Wnt-ß-catenin signalling, which is crucial for osteoblast differentiation and for bone resorption, is driven by critical inhibitors such as sclerostin (SOST) and dickkopf-related protein 1 (DKK1). As such, the aim of this study was to evaluate the involvement of SOST and DKK1 in human chronic periodontitis. MATERIAL AND METHODS: Gingival biopsies and serum were sampled from systemically healthy non-periodontitis (n = 15) and chronic periodontitis subjects (n = 15). The mRNA and protein levels of SOST, DKK1 and TNF-α in periodontal tissues were measured by qPCR and by enzyme-linked immunosorbent assay (ELISA) respectively. Serum levels of SOST, DKK1 and TNF-α were assessed by ELISA. RESULTS: The mRNA and protein levels of SOST, DKK1 and TNF-α were significantly increased in the gingival tissues of the chronic periodontitis when compared to the non-periodontitis group (p < 0.05). In addition, circulating levels of SOST and TNF-α, but not DKK1, were higher in the periodontitis group than in the non-periodontitis group (p < 0.05). CONCLUSION: SOST and DKK1 were upregulated in the periodontal tissues of chronic periodontitis subjects, suggesting a possible role of these molecules on periodontal tissues.


Asunto(s)
Proteínas Morfogenéticas Óseas/análisis , Periodontitis Crónica/metabolismo , Péptidos y Proteínas de Señalización Intercelular/análisis , Vía de Señalización Wnt/fisiología , Proteínas Adaptadoras Transductoras de Señales , Adulto , Pérdida de Hueso Alveolar/metabolismo , Proteínas Morfogenéticas Óseas/sangre , Femenino , Marcadores Genéticos , Encía/química , Humanos , Péptidos y Proteínas de Señalización Intercelular/sangre , Masculino , Persona de Mediana Edad , Pérdida de la Inserción Periodontal/metabolismo , Índice Periodontal , Bolsa Periodontal/metabolismo , ARN Mensajero/análisis , Factor de Necrosis Tumoral alfa/análisis , Factor de Necrosis Tumoral alfa/sangre , Regulación hacia Arriba
6.
Reprod Fertil Dev ; 24(5): 723-32, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22697122

RESUMEN

This study investigated the stability of housekeeping genes (glyceraldehyde-3-phosphate dehydrogenase, ß-tubulin, ß-actin, phosphoglycerate kinase (PGK), 18S rRNA, ubiquitin and ribosomal protein 19) and the levels of mRNA for bone morphogenetic protein-2 (BMP-2), -4 (BMP-4), -6 (BMP-6), -7 (BMP-7) and -15 (BMP-15), their receptors (BMPR-IA, -IB and -II) and Similar to Mothers Against Decapentaplegic (SMADs) (-1, -5 and -8) in goat follicles of 0.2, 0.5 and 1.0mm, as well as in secondary follicles before and after culture for 18 days. ß-tubulin and PGK were the most stable housekeeping genes and the levels of mRNA for BMP-2 in follicles of 0.2mm were higher than in follicles of 0.5 and 1.0mm. For BMP-4, -6 and -7, the highest levels of mRNA were found in follicles of 1.0mm. The expression of BMPR-IB was higher in follicles of 0.2mm, whereas the levels of BMPR-II were higher in follicles of 0.5mm. The levels of mRNA for SMAD-5 were higher in follicles of 0.2mm, whereas SMAD-8 had higher levels in 0.5-mm follicles. After culture, follicles showed increased levels of mRNA for BMP-2 and reduced mRNA for BMP-4, BMP-7, BMPR-IA and SMAD-5. In conclusion, ß-tubulin and PGK are the most stable reference genes, and BMPs, their receptors and SMADs have variable levels of mRNA in the follicular size classes analysed.


Asunto(s)
Receptores de Proteínas Morfogenéticas Óseas/genética , Proteínas Morfogenéticas Óseas/genética , Cabras/genética , Folículo Ovárico/metabolismo , Proteínas Smad/genética , Animales , Receptores de Proteínas Morfogenéticas Óseas/análisis , Receptores de Proteínas Morfogenéticas Óseas/metabolismo , Proteínas Morfogenéticas Óseas/análisis , Proteínas Morfogenéticas Óseas/metabolismo , Tamaño de la Célula , Células Cultivadas , Femenino , Cabras/metabolismo , Cabras/fisiología , Folículo Ovárico/citología , Folículo Ovárico/fisiología , Estabilidad Proteica , ARN Mensajero/análisis , ARN Mensajero/genética , ARN Mensajero/metabolismo , Proteínas Smad/análisis , Proteínas Smad/metabolismo , Factores de Tiempo
7.
R. bras. Reprod. Anim. ; 34(1): 3-20, 2010. ilus
Artículo en Portugués | VETINDEX | ID: vti-4618

RESUMEN

A foliculogênese é coordenada por diversos fatores de crescimento e hormônios responsáveis por garantir o sucesso do desenvolvimento folicular e oocitário. Para a obtenção de oócitos competentes, é necessária uma perfeita interação entre as células somáticas foliculares e o oócito, sendo esta potencialmente regulada por fatores parácrinos produzidos no ovário. Dentre estes fatores, destacam-se a BMP-15 e o KL, sintetizados pelo oócito e pelas células da granulosa, respectivamente. Este artigo revisa o importante papel da BMP-15 e do KL na foliculogênese, enfocando suas características, sítios de expressão, receptores e vias de sinalização, bem como a interação entre estas duas substâncias(AU)


Folliculogenesis is coordinated by many growth factors and hormones responsible for ensuring the success of follicular and oocyte development. To obtain competent oocytes is necessary to have a perfect interaction between follicular somatic cells and the oocyte, which is potentially regulated by paracrine factors produced in the ovary. Among these factors, we highlight BMP-15 and KL, synthesized by the oocyte and granulosa cells, respectively. This article reviews the important role of BMP-15 and KL in folliculogenesis, focusing on their characteristics, sites of expression, receptors and signaling pathways, as well as the interaction between these two substances(AU)


Asunto(s)
Animales , Proteínas Morfogenéticas Óseas/efectos adversos , Proteínas Morfogenéticas Óseas/análisis , Mamíferos/genética , Fertilidad
8.
Rev. bras. reprod. anim ; 34(1): 3-20, 2010. ilus
Artículo en Portugués | VETINDEX | ID: biblio-1491936

RESUMEN

A foliculogênese é coordenada por diversos fatores de crescimento e hormônios responsáveis por garantir o sucesso do desenvolvimento folicular e oocitário. Para a obtenção de oócitos competentes, é necessária uma perfeita interação entre as células somáticas foliculares e o oócito, sendo esta potencialmente regulada por fatores parácrinos produzidos no ovário. Dentre estes fatores, destacam-se a BMP-15 e o KL, sintetizados pelo oócito e pelas células da granulosa, respectivamente. Este artigo revisa o importante papel da BMP-15 e do KL na foliculogênese, enfocando suas características, sítios de expressão, receptores e vias de sinalização, bem como a interação entre estas duas substâncias


Folliculogenesis is coordinated by many growth factors and hormones responsible for ensuring the success of follicular and oocyte development. To obtain competent oocytes is necessary to have a perfect interaction between follicular somatic cells and the oocyte, which is potentially regulated by paracrine factors produced in the ovary. Among these factors, we highlight BMP-15 and KL, synthesized by the oocyte and granulosa cells, respectively. This article reviews the important role of BMP-15 and KL in folliculogenesis, focusing on their characteristics, sites of expression, receptors and signaling pathways, as well as the interaction between these two substances


Asunto(s)
Animales , Mamíferos/genética , Proteínas Morfogenéticas Óseas/análisis , Proteínas Morfogenéticas Óseas/efectos adversos , Fertilidad
9.
Arch Oral Biol ; 53(1): 2-8, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17803954

RESUMEN

There are no reports in literature about roles of bone morphogenetic protein 4 (BMP-4) in tooth development in mammals with complete dentition (with all dental groups). The classical model of study is the mouse, which has distinctive incisor and molar patterns. The opossum Didelphis albiventris with five upper and four lower incisors, one canine, three premolars and four molars, on each side of the jaw, seems to be a convenient model for odontogenesis study. This investigation searched for similarities and differences in BMP-4 expression pattern between the opossum and the mouse. BMP-4 cDNA was obtained by RT-PCR and the expression pattern during molar tooth development was investigated by the immunoperoxidase method. Opossum BMP-4 mature protein has 95% of sequence similarity in relation to mouse and 94% to human. The BMP-4 expression pattern during opossum tooth development was suggestive of a role in dental organ initiation and morphogenesis.


Asunto(s)
Proteínas Morfogenéticas Óseas/fisiología , Didelphis/fisiología , Regulación del Desarrollo de la Expresión Génica , Odontogénesis/fisiología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Proteína Morfogenética Ósea 4 , Proteínas Morfogenéticas Óseas/análisis , Proteínas Morfogenéticas Óseas/genética , ADN Complementario/análisis , Dentición , Didelphis/crecimiento & desarrollo , Humanos , Técnicas para Inmunoenzimas , Ratones , Modelos Animales , Diente Molar , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Análisis de Secuencia de ADN , Homología de Secuencia
10.
Braz Oral Res ; 21(2): 127-33, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17589647

RESUMEN

A comparative nonisotopic in situ hybridization (ISH) analysis was carried out for the detection of Bmp-4, Shh and Wnt-5a transcripts during mice odontogenesis from initiation to cap stage. Bmp-4 was expressed early in the epithelium and then in the underlying mesenchyme. Shh expression was seen in the odontogenic epithelial lining thickening, being stronger in the enamel knot area, during the cap stage. Wnt-5a transcripts were expressed only in the mesenchyme during the initiation, bud and cap stages, with strong expression in the dental mesenchyme during the bud stage. The present results showed that Bmp-4, Shh and Wnt-5a are expressed since the very early stages of tooth development, and they suggest that the Wnt-5a gene is expressed in different cell populations than Bmp-4 and Shh.


Asunto(s)
Proteínas Morfogenéticas Óseas/análisis , Proteínas Hedgehog/análisis , Odontogénesis/fisiología , Proteínas Wnt/análisis , Animales , Proteínas Morfogenéticas Óseas/genética , Modelos Animales de Enfermedad , Expresión Génica/fisiología , Regulación del Desarrollo de la Expresión Génica , Proteínas Hedgehog/genética , Hibridación in Situ , Ratones , Ratones Endogámicos C57BL , Odontogénesis/genética , Germen Dentario/citología , Germen Dentario/embriología , Transcripción Genética , Proteínas Wnt/genética
11.
Braz. oral res ; 21(2): 127-133, 2007. ilus
Artículo en Inglés | LILACS | ID: lil-453191

RESUMEN

A comparative nonisotopic in situ hybridization (ISH) analysis was carried out for the detection of Bmp-4, Shh and Wnt-5a transcripts during mice odontogenesis from initiation to cap stage. Bmp-4 was expressed early in the epithelium and then in the underlying mesenchyme. Shh expression was seen in the odontogenic epithelial lining thickening, being stronger in the enamel knot area, during the cap stage. Wnt-5a transcripts were expressed only in the mesenchyme during the initiation, bud and cap stages, with strong expression in the dental mesenchyme during the bud stage. The present results showed that Bmp-4, Shh and Wnt-5a are expressed since the very early stages of tooth development, and they suggest that the Wnt-5a gene is expressed in different cell populations than Bmp-4 and Shh.


No presente trabalho, realizou-se uma análise comparativa não isotópica por hibridização in situ a fim de se detectar a presença de transcritos de Bmp-4, Shh e Wnt-5a durante as fases iniciais da odontogênese em camundongos, desde a iniciação até o estágio de capuz. No estágio de iniciação, observou-se expressão precoce de Bmp-4 no epitélio e no mesênquima subjacente, enquanto que a expressão de Shh ocorreu durante o estágio de capuz, na região de espessamento do revestimento epitelial odontogênico, tornando-se mais intensa na área de nó do esmalte. Os transcritos de Wnt-5a foram expressos somente no mesênquima durante os estágios de iniciação, botão e capuz, com intenso sinal na região no mesênquima na fase de botão. Estes resultados mostraram que Bmp-4, Shh e Wnt-5a são expressos desde os estágios mais precoces do desenvolvimento dentário, sugerindo que o gene Wnt-5a seja expresso em populações celulares distintas daquelas que expressam Bmp-4 e Shh.


Asunto(s)
Animales , Ratones , Proteínas Morfogenéticas Óseas/análisis , Proteínas Hedgehog/análisis , Odontogénesis/fisiología , Proteínas Wnt/análisis , Proteínas Morfogenéticas Óseas/genética , Modelos Animales de Enfermedad , Regulación del Desarrollo de la Expresión Génica , Expresión Génica/fisiología , Proteínas Hedgehog/genética , Hibridación in Situ , Odontogénesis/genética , Transcripción Genética , Germen Dentario/citología , Germen Dentario/embriología , Proteínas Wnt/genética
12.
Bauru; s.n; 1999. 104 p. ilus.
Tesis en Portugués | LILACS, BBO - Odontología | ID: lil-256158

RESUMEN

A reabsorçäo dentária fisiológica ou rizólise em dentes decíduos, representa um fenômeno natural e programado pelo organismo, seguido pela substituiçäo da dentiçäo temporária pela permanente. Para estudar os mecanismos e mediadores bioquímicos envolvidos na induçäo da reabsorçäo fisiológica foram utilizados caninos e incisivos decíduos de gatos, em diferentes estádios de rizólise. Os animais utilizados tinham aproximadamente dois meses de vida pós-natal. O caráter programado da reabsorçäo dentária fisiológica motivou o estudo da participaçäo da apoptose neste processo. A apoptose foi evidenciada pela técnica TUNEL modificada nos cementoblastos, fibroblastos do tecido pulpar, do ligamento periodontal e nos restos epiteliais de Malassez dos dentes decíduos. A partir desta marcaçäo buscou-se identificar os prováveis mediadores bioquímicos indutores da apoptose nestas células, utilizando-se da hibridizaçäo in situ com radiosótopos. Uma das proteínas envolvidas na induçäo da apoptose em eventos fisiológicos, a proteína morfogenética óssea 4 (BMP-4), foi detectada nos cementoblastos e células do ligamento periodontal do dente decíduo. Topograficamente observou-se uma similaridade entre a expressäo de Bmp-4 e a técnica TUNEL modificada em cortes idênticos. Uma intensa marcaçäo de Bmp-4 foi também observada nos ameloblastos do dente permanente. Para a análise da participaçäo dos clastos na rizólise, foi avaliada via hibridizaçäo in situ, a expressäo de gelatinase B, uma metaproteinase da matriz extracelular sintetizada por estas células...


Asunto(s)
Animales , Masculino , Femenino , Lactante , Gatos , Apoptosis/fisiología , Resorción Dentaria/clasificación , Resorción Dentaria/fisiopatología , Diente Primario/fisiopatología , Gelatinasas/análisis , Patología Bucal , Patología Bucal/clasificación , Proteínas Morfogenéticas Óseas/análisis , Resorción Dentaria/enzimología
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