日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Symptoms of Long-COVID 1-Year after a COVID-19 outbreak among sailors on a French aircraft carrier

法国航母水兵新冠疫情爆发一年后出现新冠长期症状

Perisse, A; De Cacqueray, F; Delarbre, D; Marsaa, H; Bergmann, C; Da Silva, V; Bronstein, A; Paleiron, N; Menoud, N; Cobola, J; Verret, C; Mayet, A; Bylicki, O

Obsessive-compulsive disorder during the COVID-19 pandemic

新冠疫情期间的强迫症

Van Ameringen, M; Patterson, B; Turna, J; Lethbridge, G; Goldman Bergmann, C; Lamberti, N; Rahat, M; Sideris, B; Francisco, A P; Fineberg, N; Pallanti, S; Grassi, G; Vismara, M; Albert, U; Gedanke Shavitt, R; Hollander, E; Feusner, J; Rodriguez, C I; Morgado, P; Dell'Osso, B

AllergoOncology: ultra-low IgE, a potential novel biomarker in cancer-a Position Paper of the European Academy of Allergy and Clinical Immunology (EAACI)

AllergoOncology:超低 IgE,一种潜在的新型癌症生物标志物——欧洲过敏与临床免疫学会 (EAACI) 的立场文件

Ferastraoaru, D; Bax, H J; Bergmann, C; Capron, M; Castells, M; Dombrowicz, D; Fiebiger, E; Gould, H J; Hartmann, K; Jappe, U; Jordakieva, G; Josephs, D H; Levi-Schaffer, F; Mahler, V; Poli, A; Rosenstreich, D; Roth-Walter, F; Shamji, M; Steveling-Klein, E H; Turner, M C; Untersmayr, E; Karagiannis, S N; Jensen-Jarolim, E

Impact of human papilloma virus infection on the response of head and neck cancers to anti-epidermal growth factor receptor antibody therapy.

人乳头瘤病毒感染对头颈癌抗表皮生长因子受体抗体治疗反应的影响

Pogorzelski M, Ting S, Gauler T C, Breitenbuecher F, Vossebein I, Hoffarth S, Markowetz J, Lang S, Bergmann C, Brandau S, Jawad J A, Schmid K W, Schuler M, Kasper S

Clinical utility gene card for: Meckel syndrome

临床实用基因卡:梅克尔综合征

Salonen, R; Kestilä, M; Bergmann, C

Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia

编码 Wnt 信号通路组分 R-spondin 4 (RSPO4) 的基因突变会导致常染色体隐性遗传性无甲症。

Bergmann, C; Senderek, J; Anhuf, D; Thiel, C T; Ekici, A B; Poblete-Gutierrez, P; van Steensel, M; Seelow, D; Nürnberg, G; Schild, H H; Nürnberg, P; Reis, A; Frank, J; Zerres, K

Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)

PKHD1基因的多外显子缺失会导致常染色体隐性多囊肾病(ARPKD)。

Bergmann, C; Küpper, F; Schmitt, C P; Vester, U; Neuhaus, T J; Senderek, J; Zerres, K

Effects of ATP on cultured smooth muscle cells from rat aorta

ATP对大鼠主动脉培养平滑肌细胞的影响

von der Weid, P Y; Serebryakov, V N; Orallo, F; Bergmann, C; Snetkov, V A; Takeda, K

Topology of the non-structural rotavirus receptor glycoprotein NS28 in the rough endoplasmic reticulum

粗面内质网中非结构性轮状病毒受体糖蛋白NS28的拓扑结构

Bergmann, C C; Maass, D; Poruchynsky, M S; Atkinson, P H; Bellamy, A R

Cloning and expression of human salivary-gland kallikrein in Escherichia coli

大肠杆菌中人唾液腺激肽释放酶的克隆和表达

Angermann, A; Bergmann, C; Appelhans, H