Detalhe da pesquisa
1.
A single-cell time-lapse of mouse prenatal development from gastrula to birth.
Nature
; 626(8001): 1084-1093, 2024 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-38355799
2.
Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy.
Am J Hum Genet
; 95(2): 227-34, 2014 Aug 07.
Artigo
Inglês
| MEDLINE | ID: mdl-25105227
3.
Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.
Am J Hum Genet
; 94(1): 62-72, 2014 Jan 02.
Artigo
Inglês
| MEDLINE | ID: mdl-24360808
4.
Cross-species imputation and comparison of single-cell transcriptomic profiles.
bioRxiv
; 2023 Oct 20.
Artigo
Inglês
| MEDLINE | ID: mdl-37905060
5.
A single-cell multi-omic atlas spanning the adult rhesus macaque brain.
Sci Adv
; 9(41): eadh1914, 2023 10 13.
Artigo
Inglês
| MEDLINE | ID: mdl-37824616
6.
A single-cell transcriptional timelapse of mouse embryonic development, from gastrula to pup.
bioRxiv
; 2023 Apr 05.
Artigo
Inglês
| MEDLINE | ID: mdl-37066300
7.
A human cell atlas of fetal chromatin accessibility.
Science
; 370(6518)2020 11 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33184180
8.
A human cell atlas of fetal gene expression.
Science
; 370(6518)2020 11 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33184181
9.
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.
Cell Rep
; 31(1): 107489, 2020 04 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32268104
10.
Marijuana use differentially affects cannabinoid receptor expression in early gestational human endometrium and placenta.
Placenta
; 66: 36-39, 2018 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29884300
11.
Abnormal glycosylation in Joubert syndrome type 10.
Cilia
; 6: 2, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28344780
12.
Keratinocytes produce IL-17c to protect peripheral nervous systems during human HSV-2 reactivation.
J Exp Med
; 214(8): 2315-2329, 2017 Aug 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28663436
13.
Hypomorphism for RPGRIP1L, a ciliary gene vicinal to the FTO locus, causes increased adiposity in mice.
Cell Metab
; 19(5): 767-79, 2014 May 06.
Artigo
Inglês
| MEDLINE | ID: mdl-24807221
14.
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Science
; 338(6114): 1619-22, 2012 Dec 21.
Artigo
Inglês
| MEDLINE | ID: mdl-23160955