Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 19

Results: 8

Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspring.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1863, doi. 10.1093/hmg/ddab154

By:

Harrison, David J;
Creeth, Hugo D J;
Tyson, Hannah R;
Boque-Sastre, Raquel;
Hunter, Susan;
Dwyer, Dominic M;
Isles, Anthony R;
John, Rosalind M

Publication type:

Article

Functional and behavioral effects of de novo mutations in calcium-related genes in patients with bipolar disorder.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1851, doi. 10.1093/hmg/ddab152

By:

Nakamura, Takumi;
Nakajima, Kazuo;
Kobayashi, Yuki;
Itohara, Shigeyoshi;
Kasahara, Takaoki;
Tsuboi, Takashi;
Kato, Tadafumi

Publication type:

Article

Identification of microRNAs and gene regulatory networks in cleft lip common in humans and mice.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1881, doi. 10.1093/hmg/ddab151

By:

Yoshioka, Hiroki;
Li, Aimin;
Suzuki, Akiko;
Ramakrishnan, Sai Shankar;
Zhao, Zhongming;
Iwata, Junichi

Publication type:

Article

Targeted HAI-2 deletion causes excessive proteolysis with prolonged active prostasin and depletion of HAI-1 monomer in intestinal but not epidermal epithelial cells.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1833, doi. 10.1093/hmg/ddab150

By:

Barndt, Robert B;
Lee, Mon-Juan;
Huang, Nanxi;
Lu, Dajun D;
Lee, See-Chi;
Du, Po-Wen;
Chang, Chun-Chia;
Tsai, Ping-Feng B;
Huang, Yu-Siou K;
Chang, Hao-Ming;
Wang, Jehng-Kang;
Lai, Chih-Hsin;
Johnson, Michael D;
Lin, Chen-Yong

Publication type:

Article

Cognitive deficits in episodic ataxia type 2 mouse models.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1811, doi. 10.1093/hmg/ddab149

By:

Bohne, Pauline;
Mourabit, Damian Boden-El;
Josten, Mareike;
Mark, Melanie D

Publication type:

Article

Toxicity of pathogenic ataxin-2 in Drosophila shows dependence on a pure CAG repeat sequence.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1797, doi. 10.1093/hmg/ddab148

By:

McGurk, Leeanne;
Rifai, Olivia M;
Shcherbakova, Oksana;
Perlegos, Alexandra E;
Byrns, China N;
Carranza, Faith R;
Zhou, Henry W;
Kim, Hyung-Jun;
Zhu, Yongqing;
Bonini, Nancy M

Publication type:

Article

Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1785, doi. 10.1093/hmg/ddab145

By:

Bassani, Sissy;
Beelen, Edward van;
Rossel, Mireille;
Voisin, Norine;
Morgan, Anna;
Arribat, Yoan;
Chatron, Nicolas;
Chrast, Jacqueline;
Cocca, Massimiliano;
Delprat, Benjamin;
Faletra, Flavio;
Giannuzzi, Giuliana;
Guex, Nicolas;
Machavoine, Roxane;
Pradervand, Sylvain;
Smits, Jeroen J;
Kamp, Jiddeke M van de;
Ziegler, Alban;
Amati, Francesca;
Marlin, Sandrine

Publication type:

Article

Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 19, p. 1894, doi. 10.1093/hmg/ddab121

By:

Beck, Jeffrey J;
Pool, René;
van de Weijer, Margot;
Chen, Xu;
Krapohl, Eva;
Gordon, Scott D;
Nygaard, Marianne;
Debrabant, Birgit;
Palviainen, Teemu;
Zee, Matthijs D van der;
Baselmans, Bart;
Finnicum, Casey T;
Yi, Lu;
Lundström, Sebastian;
Beijsterveldt, Toos van;
Christiansen, Lene;
Heikkilä, Kauko;
Kittelsrud, Julie;
Loukola, Anu;
Ollikainen, Miina

Publication type:

Article