skip to main content
Idioma:
Primo Advanced Search
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search prefilters
Busca Simples
Resultados 1 2 3 next page
Mostrar Somente
Refinado por: assunto: eng remover assunto: Science & Technology remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Cross-Talk between Mucosal-Associated Invariant T, Natural Killer, and Natural Killer T Cell Populations is Implicated in the Pathogenesis of Placenta Accreta Spectrum
Cross-Talk between Mucosal-Associated Invariant T, Natural Killer, and Natural Killer T Cell Populations is Implicated in the Pathogenesis of Placenta Accreta Spectrum
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cross-Talk between Mucosal-Associated Invariant T, Natural Killer, and Natural Killer T Cell Populations is Implicated in the Pathogenesis of Placenta Accreta Spectrum

El-Badawy, Omnia ; Abbas, Ahmed M. ; Radwan, Eman ; Makboul, Rania ; Khamis, Areej A. ; Ali, Maha ; Elkabsh, Mai M. ; Bakr, Marwa H. ; Zahran, Asmaa M.

Inflammation, 2023-08, Vol.46 (4), p.1192-1208 [Periódico revisado por pares]

New York: Springer US

Texto completo disponível

Citações Citado por
2
Tunable Compact Metamaterial-Based Double-Negative/Near-Zero Index Resonator for 6G Terahertz Wireless Applications
Tunable Compact Metamaterial-Based Double-Negative/Near-Zero Index Resonator for 6G Terahertz Wireless Applications
Material Type:
Artigo 		Adicionar ao Meu Espaço

Tunable Compact Metamaterial-Based Double-Negative/Near-Zero Index Resonator for 6G Terahertz Wireless Applications

Musaed, Alya Ali ; Al-Bawri, Samir Salem ; Islam, Mohammad Tariqul ; Al-Gburi, Ahmed Jamal Abdullah ; Singh, Mandeep Jit

Materials, 2022-08, Vol.15 (16), p.5608 [Periódico revisado por pares]

Basel: MDPI AG

Texto completo disponível

Citações Citado por
3
Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia
Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia

Kitayama, Kana ; Ishiguro, Tomoya ; Komiyama, Masaki ; Morisaki, Takayuki ; Morisaki, Hiroko ; Minase, Gaku ; Hamanaka, Kohei ; Miyatake, Satoko ; Matsumoto, Naomichi ; Kato, Masaru ; Takahashi, Toru ; Yorifuji, Tohru

BMC medical genomics, 2021-12, Vol.14 (1), p.288-288, Article 288 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
4
Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary
Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary
Material Type:
Artigo 		Adicionar ao Meu Espaço

Current Status of Clinical and Genetic Screening of Hereditary Hemorrhagic Telangiectasia Families in Hungary

Major, Tamás ; Bereczky, Zsuzsanna ; Gindele, Réka ; Balogh, Gábor ; Rácz, Benedek ; Bora, László ; Kézsmárki, Zsolt ; Brúgós, Boglárka ; Pfliegler, György

Journal of clinical medicine, 2021-08, Vol.10 (17), p.3774 [Periódico revisado por pares]

Basel: MDPI AG

Texto completo disponível

Citações Citado por
5
Recording and manipulation of vagus nerve electrical activity in chronically instrumented unanesthetized near term fetal sheep
Recording and manipulation of vagus nerve electrical activity in chronically instrumented unanesthetized near term fetal sheep
Material Type:
Artigo 		Adicionar ao Meu Espaço

Recording and manipulation of vagus nerve electrical activity in chronically instrumented unanesthetized near term fetal sheep

Castel, Aude ; Burns, Patrick M. ; Benito, Javier ; Liu, Hai L. ; Kuthiala, Shikha ; Durosier, Lucien D. ; Frank, Yael ; Cao, Mingju ; Paquet, Marilène ; Fecteau, Gilles ; Desrochers, André ; Frasch, Martin G.

Journal of neuroscience methods, 2021-08, Vol.360, p.109257-109257, Article 109257 [Periódico revisado por pares]

Elsevier B.V

Texto completo disponível

Citações Citado por
6
A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer
A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer
Material Type:
Artigo 		Adicionar ao Meu Espaço

A distinct repertoire of cancer‐associated fibroblasts is enriched in cribriform prostate cancer

Hesterberg, Amanda B ; Rios, Brenda L ; Wolf, Elysa M ; Tubbs, Colby ; Wong, Hong Yuen ; Schaffer, Kerry R ; Lotan, Tamara L ; Giannico, Giovanna A ; Gordetsky, Jennifer B ; Hurley, Paula J

The Journal of Pathology: Clinical Research, 2021-05, Vol.7 (3), p.271-286 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
7
The clinical and genetic features of hereditary haemorrhagic telangiectasia (HHT) in central South Africa—three novel pathogenic variants
The clinical and genetic features of hereditary haemorrhagic telangiectasia (HHT) in central South Africa—three novel pathogenic variants
Material Type:
Artigo 		Adicionar ao Meu Espaço

The clinical and genetic features of hereditary haemorrhagic telangiectasia (HHT) in central South Africa—three novel pathogenic variants

Mutize, Tendaishe T. ; Seedat, Riaz Y. ; Ploos van Amstel, Johannes K. ; Mager, Johannes J. ; Brown, Stephen C. ; Gebremariam, Fekade ; Coetzee, Marius J.

Molecular biology reports, 2020-12, Vol.47 (12), p.9967-9972 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

Texto completo disponível

Citações Citado por
8
Genotype-Phenotype Correlations in Children with HHT
Genotype-Phenotype Correlations in Children with HHT
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genotype-Phenotype Correlations in Children with HHT

Kilian, Alexandra ; Latino, Giuseppe A ; White, Andrew J ; Clark, Dewi ; Chakinala, Murali M ; Ratjen, Felix ; McDonald, Jamie ; Whitehead, Kevin ; Gossage, James R ; Lin, Doris ; Henderson, Katharine ; Pollak, Jeffrey ; McWilliams, Justin P ; Kim, Helen ; Lawton, Michael T ; Faughnan, Marie E

Journal of clinical medicine, 2020-08, Vol.9 (9), p.2714 [Periódico revisado por pares]

Switzerland: MDPI AG

Texto completo disponível

Citações Citado por
9
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1

Snellings, Daniel A. ; Gallione, Carol J. ; Clark, Dewi S. ; Vozoris, Nicholas T. ; Faughnan, Marie E. ; Marchuk, Douglas A.

American journal of human genetics, 2019-11, Vol.105 (5), p.894-906 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
10
Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia
Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia

Zhao, Yali ; Zhang, Yuan ; Wang, Xiangdong ; Zhang, Luo

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e893-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
Resultados 1 2 3 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (29)
  2. Revistas revisadas por pares (28)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (29)
  2. Livros  (1)
  3. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de2006  (4)
  2. 2006Até2008  (7)
  3. 2009Até2012  (4)
  4. 2013Até2018  (6)
  5. Após 2018  (10)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.