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

Preclinical research (on rare diseases): we need to talk about health equity

(罕见病)临床前研究:我们需要探讨健康公平问题。

Greenfield, Andy

Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice

Znrf3缺陷小鼠的性腺性别逆转以单细胞分辨率呈现

Kay, Raissa G G; Reeves, Richard; Siggers, Pam; Greenaway, Simon; Mallon, Ann-Marie; Wells, Sara; Koo, Bon-Kyoung; Mayère, Chloé; Nef, Serge; Greenfield, Andy; Simon, Michelle M

PMON312 A De Novo Heterozygous Nonsense Variant In The SEC31A Gene Associated With Pituitary Hormone Deficiency And Disorders Of Sex Development

PMON312 是 SEC31A 基因中一种与垂体激素缺乏和性发育障碍相关的从头杂合无义变异

Bernreuther, Christian; Flitsch, Jörg; Lüdecke, Dieter K; Hagel, Christian; Greenfield, Andy; Herzyk, Pawel; Lucas-Herald, Angela K; McGowan, Ruth; SGP, Scottish Genomes Partnership; Touyz, Rhian M; Williams, Nicola; Tobias, Edward S; Sagar, Danielle; Montezano, Augusto C; Rios, Francisco J; de Lucca Camargo, Livia; Hamilton, Graham; Gazdagh, Gabriella

Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high-normal testicular volume

两名患有尿道下裂、原发性性腺功能减退症和睾丸体积处于正常高值的男性兄弟携带一种新的INHA突变纯合子。

Arslan Ates, Esra; Eltan, Mehmet; Sahin, Bahadir; Gurpinar Tosun, Busra; Seven Menevse, Tuba; Geckinli, Bilgen Bilge; Greenfield, Andy; Turan, Serap; Bereket, Abdullah; Guran, Tulay

Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C

PPP2R3C基因L193S纯合变异患者出现广谱XX和XY性腺发育不全

Cicek, Dilek; Warr, Nick; Yesil, Gozde; Kocak Eker, Hatice; Bas, Firdevs; Poyrazoglu, Sukran; Darendeliler, Feyza; Direk, Gul; Hatipoglu, Nihal; Eltan, Mehmet; Yavas Abali, Zehra; Gurpinar Tosun, Busra; Kaygusuz, Sare Betul; Seven Menevse, Tuba; Helvacioglu, Didem; Turan, Serap; Bereket, Abdullah; Reeves, Richard; Simon, Michelle; Mackenzie, Matthew; Teboul, Lydia; Greenfield, Andy; Guran, Tulay

ISSCR Guidelines for Stem Cell Research and Clinical Translation: The 2021 update

国际干细胞研究学会(ISSCR)干细胞研究和临床转化指南:2021年更新版

Lovell-Badge, Robin; Anthony, Eric; Barker, Roger A; Bubela, Tania; Brivanlou, Ali H; Carpenter, Melissa; Charo, R Alta; Clark, Amander; Clayton, Ellen; Cong, Yali; Daley, George Q; Fu, Jianping; Fujita, Misao; Greenfield, Andy; Goldman, Steve A; Hill, Lori; Hyun, Insoo; Isasi, Rosario; Kahn, Jeffrey; Kato, Kazuto; Kim, Jin-Soo; Kimmelman, Jonathan; Knoblich, Jürgen A; Mathews, Debra; Montserrat, Nuria; Mosher, Jack; Munsie, Megan; Nakauchi, Hiromitsu; Naldini, Luigi; Naughton, Gail; Niakan, Kathy; Ogbogu, Ubaka; Pedersen, Roger; Rivron, Nicolas; Rooke, Heather; Rossant, Janet; Round, Jeff; Saitou, Mitinori; Sipp, Douglas; Steffann, Julie; Sugarman, Jeremy; Surani, Azim; Takahashi, Jun; Tang, Fuchou; Turner, Leigh; Zettler, Patricia J; Zhai, Xiaomei

ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling

ZNRF3通过抑制经典WNT信号通路在哺乳动物性别决定中发挥作用

Harris, Abigail; Siggers, Pam; Corrochano, Silvia; Warr, Nick; Sagar, Danielle; Grimes, Daniel T; Suzuki, Makoto; Burdine, Rebecca D; Cong, Feng; Koo, Bon-Kyoung; Clevers, Hans; Stévant, Isabelle; Nef, Serge; Wells, Sara; Brauner, Raja; Ben Rhouma, Bochra; Belguith, Neïla; Eozenou, Caroline; Bignon-Topalovic, Joelle; Bashamboo, Anu; McElreavey, Ken; Greenfield, Andy

CRISPR-Cas9-Mediated Mutagenesis: Mind the Gap?

CRISPR-Cas9介导的诱变:注意差距?

Teboul, Lydia; Greenfield, Andy

Characterisation and use of a functional Gadd45g bacterial artificial chromosome

功能性 Gadd45g 细菌人工染色体的特性分析和应用

Warr, Nick; May, Joel; Teboul, Lydia; Suzuki, Toru; Asami, Maki; Perry, Anthony C F; Wells, Sara; Greenfield, Andy

Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia

斑马鱼21-羟化酶基因缺失导致肾间质增生

Eachus, Helen; Zaucker, Andreas; Oakes, James A; Griffin, Aliesha; Weger, Meltem; Güran, Tülay; Taylor, Angela; Harris, Abigail; Greenfield, Andy; Quanson, Jonathan L; Storbeck, Karl-Heinz; Cunliffe, Vincent T; Müller, Ferenc; Krone, Nils