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1.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.
Am J Hum Genet
; 99(1): 236-45, 2016 Jul 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27392078
2.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.
Am J Hum Genet
; 102(4): 713, 2018 04 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29625027
3.
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice.
BMC Dev Biol
; 15: 27, 2015 Jul 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-26134413
4.
Outcomes in Pulmonary Hypertension in Relation to Insurance Status: National Hospital Discharge Survey, 2000-2010.
Turk Thorac J
; 22(2): 182-183, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33871345
5.
[Microbial contamination of surfaces in the departments of Medicine and Surgery: single center prevalence study in Sassari (Italy)]. / Contaminazioni microbiche di superfici di frequente contatto in reparti di medicina e chirurgia: studio monocentrico di prevalenza a Sassari.
Recenti Prog Med
; 107(1): 50-4, 2016 Jan.
Artículo
en Italiano
| MEDLINE | ID: mdl-26901369
6.
Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosis.
Bone
; 59: 122-6, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24269275
7.
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity.
PLoS One
; 5(3): e9477, 2010 Mar 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-20209145
8.
Withania somnifera prevents morphine withdrawal-induced decrease in spine density in nucleus accumbens shell of rats: a confocal laser scanning microscopy study.
Neurotox Res
; 16(4): 343-55, 2009 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-19551457
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