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

Challenges past, present and future for Endocrine Connections

内分泌连接杂志过去、现在和未来的挑战

Clark, Adrian J L

Fake science for sale? How Endocrine Connections is tackling paper mills

伪科学出售?《内分泌连接》杂志如何打击造纸厂

Clark, Adrian J L; Buckmaster, Simon

ACTH signalling and adrenal development: lessons from mouse models

ACTH信号传导与肾上腺发育:来自小鼠模型的启示

Novoselova, Tatiana V; King, Peter J; Guasti, Leonardo; Metherell, Louise A; Clark, Adrian J L; Chan, Li F

Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid

母体蛋白质限制后新生大鼠基因组甲基化和基因表达的变化以及叶酸逆转这些变化

Altobelli, Gioia; Bogdarina, Irina G; Stupka, Elia; Clark, Adrian J L; Langley-Evans, Simon

MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans

MCM4基因突变会导致人类肾上腺功能衰竭、身材矮小和自然杀伤细胞缺乏。

Hughes, Claire R; Guasti, Leonardo; Meimaridou, Eirini; Chuang, Chen-Hua; Schimenti, John C; King, Peter J; Costigan, Colm; Clark, Adrian J L; Metherell, Louise A

An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W)

一例非典型家族性糖皮质激素缺乏症,无色素沉着,由 MC2R (T152K) 和 MC1R (R160W) 基因的纯合突变同时存在引起。

Turan, Serap; Hughes, Claire; Atay, Zeynep; Guran, Tulay; Haliloglu, Belma; Clark, Adrian J L; Bereket, Abdullah; Metherell, Louise A

The cytosolic chaperone Hsc70 promotes traffic to the cell surface of intracellular retained melanocortin-4 receptor mutants.

胞质分子伴侣 Hsc70 促进细胞内滞留的黑皮质素-4 受体突变体向细胞表面的运输

Meimaridou Eirini, Gooljar Sakina B, Ramnarace Nalini, Anthonypillai Lucia, Clark Adrian J L, Chapple J Paul

12-Lipoxygenase Products Reduce Insulin Secretion and β-Cell Viability in Human Islets

12-脂氧合酶产物降低人胰岛的胰岛素分泌和β细胞活力

Nadolsky, Karl Z; David, Alessia; Srirangalingam, Umasuthan; Metherell, Louise A; Khoo, Bernard; Clark, Adrian J L; Dateki, Sumito; Kosaka, Kitaro; Hasegawa, Kosei; Tanaka, Hiroyuki; Azuma, Noriyuki; Yokoya, Susumu; Muroya, Koji; Adachi, Masanori; Tajima, Toshihiro; Motomura, Katsuaki; Kinoshita, Eiichi; Moriuchi, Hiroyuki; Sato, Naoko; Fukami, Maki; Ogata, Tsutomu; Ma, K; Nunemaker, C S; Wu, R; Chakrabarti, S K; Taylor-Fishwick, D A; Nadler, J L

Repair of Aberrant Splicing in Growth Hormone Receptor by Antisense Oligonucleotides Targeting the Splice Sites of a Pseudoexon

利用靶向假外显子剪接位点的反义寡核苷酸修复生长激素受体中的异常剪接

Burton, K; David, Alessia; Srirangalingam, Umasuthan; Metherell, Louise A; Khoo, Bernard; Clark, Adrian J L

Functional consequence of a novel Y129C mutation in a patient with two contradictory melanocortin-2-receptor mutations

一例携带两种相互矛盾的黑素皮质素-2受体突变的患者中,一种新的Y129C突变的功能后果

Chan, Li F; Chung, Teng-Teng; Massoud, Ahmed F; Metherell, Louise A; Clark, Adrian J L