Apold相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

The training and development process during childhood and adolescence of a multiple Ballon d'Or-nominated soccer player

一位多次获得金球奖提名的足球运动员在童年和青少年时期的训练和发展过程

期刊:Frontiers in Sports and Active Living

影响因子:2.6

doi:10.3389/fspor.2025.1710194

Tønnessen, Espen; Sandbakk, Silvana Bucher; Apold-Aasen, Sigmund; Sandbakk, Øyvind; Haugen, Thomas A

发表日期：2025

文献求助收藏

Reverse Shoulder Arthroplasty Is Superior to Plate Fixation at 2 Years for Displaced Proximal Humeral Fractures in the Elderly: A Multicenter Randomized Controlled Trial

一项多中心随机对照试验表明，对于老年移位性肱骨近端骨折患者，反向肩关节置换术在2年时优于钢板固定术。

期刊:Journal of Bone and Joint Surgery

影响因子:4.3

doi:10.2106/JBJS.19.01071

Fraser, Alexander Nilsskog; Bjørdal, Jonas; Wagle, Tone Mehlum; Karlberg, Anna Cecilia; Lien, Odd Arve; Eilertsen, Lars; Mader, Konrad; Apold, Hilde; Larsen, Leif Børge; Madsen, Jan Erik; Fjalestad, Tore

发表日期：2020

文献求助收藏

Risk factors for knee replacement due to primary osteoarthritis, a population based, prospective cohort study of 315,495 individuals

一项基于人群的前瞻性队列研究，纳入315,495名受试者，探讨原发性骨关节炎导致膝关节置换的风险因素。

期刊:BMC Musculoskeletal Disorders

影响因子:2.4

doi:10.1186/1471-2474-15-217

Apold, Hilde; Meyer, Haakon E; Nordsletten, Lars; Furnes, Ove; Baste, Valborg; Flugsrud, Gunnar B

发表日期：2014

文献求助收藏

High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series

前瞻性研究证实了BRCA1和BRCA2突变的高外显率

期刊:Hereditary Cancer in Clinical Practice

影响因子:2.4

doi:10.1186/1897-4287-8-2

Møller, Pål; Mæhle, Lovise; Engebretsen, Lars F; Ludvigsen, Trond; Jonsrud, Christoffer; Apold, Jaran; Vabø, Anita; Clark, Neal

发表日期：2010

文献求助收藏

Survival in Norwegian BRCA1 mutation carriers with breast cancer

挪威BRCA1基因突变携带者乳腺癌患者的生存情况

期刊:Hereditary Cancer in Clinical Practice

影响因子:2.4

doi:10.1186/1897-4287-7-7

Hagen, Anne Irene; Tretli, Steinar; Maehle, Lovise; Apold, Jaran; Vedå, Nina; Møller, Pål

发表日期：2009

文献求助收藏

No sib pair concordance for breast or ovarian cancer in BRCA1 mutation carriers

BRCA1基因突变携带者中，同胞患乳腺癌或卵巢癌的一致性并不显著。

期刊:Hereditary Cancer in Clinical Practice

影响因子:2.4

doi:10.1186/1897-4287-5-2-67

Møller, Pål; Maehle, Lovise; Clark, Neal; Apold, Jaran

发表日期：2007

文献求助收藏

Germline PTEN mutations are rare and highly penetrant

生殖系PTEN突变罕见且外显率很高。

期刊:Hereditary Cancer in Clinical Practice

影响因子:2.4

doi:10.1186/1897-4287-4-4-177

Rustad, Cecilie F; Bjørnslett, Merete; Heimdal, Ketil R; Mæhle, Lovise; Apold, Jaran; Møller, Pål

发表日期：2006

文献求助收藏

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

常见的BRCA1突变1135insA有多种起源：不同人群的单倍型研究

期刊:BMC Medical Genetics

doi:10.1186/1471-2350-7-15

Rudkin, Teresa M; Hamel, Nancy; Galvez, Maria; Hogervorst, Frans; Gille, Johan J P; Møller, Pål; Apold, Jaran; Foulkes, William D

发表日期：2006

文献求助收藏

Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from Norway

对来自挪威的61名家族性乳腺癌患者的BRCA1基因进行了完整的突变筛查和单倍型分析。

期刊:Disease Markers

doi:10.1155/2005/542928

Frost, Petter; Jugessur, Astanand; Apold, Jaran; Heimdal, Ketil; Aloysius, Thomas; Eliassen, Aud K; Fauske, Lars; Matre, Guri; Eiken, Hans Geir

发表日期：2005

文献求助收藏

Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme

在大肠杆菌中表达重组人苯丙氨酸羟化酶融合蛋白可避免宿主细胞蛋白酶的蛋白水解降解。分离和鉴定野生型酶

期刊:Biochemical Journal

影响因子:4.3

doi:10.1042/bj3060589

Martinez, A; Knappskog, P M; Olafsdottir, S; Døskeland, A P; Eiken, H G; Svebak, R M; Bozzini, M; Apold, J; Flatmark, T

细胞生物学

发表日期：1995

文献求助收藏