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Human Mutation
|
September 9, 2020
Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene
Francesca Piceci-Sparascio, Adrian Palencia-Campos, Patricia Soto-Bielicka, et al.
European Journal of Human Genetics : EJHG
|
September 30, 2025
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder
Asier Iturrate, Nurit Assia Batzir, Ranit Jaron, et al.
Frontiers in Oncology
|
March 9, 2026
Advances in intratumoral immunotherapy from a neuro-immune-endocrine perspective for breast cancer treatment
Claudia Angélica Garay-Canales, Mariana Segovia-Mendoza, Yair Rodríguez-Santiago, et al.
The Science of the Total Environment
|
January 25, 2016
Airborne pollen trends in the Iberian Peninsula
C Galán, P Alcázar, J Oteros, et al.
Journal of Medicinal Chemistry
|
March 4, 1998
Discovery of ritonavir, a potent inhibitor of HIV protease with high oral bioavailability and clinical efficacy
D J Kempf, H L Sham, K C Marsh, et al.
American Journal of Human Genetics
|
June 13, 1998
Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region
S Monk, A Sakuntabhai, S A Carter, et al.
Cell Reports
|
March 23, 2022
A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell
Mayra L Ruiz Tejada Segura, Eman Abou Moussa, Elisa Garabello, et al.
Frontiers in Medicine
|
December 12, 2025
Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in <i>FAM83G</i>
Mónica Mora-Gómez, Marta Feito, Natalia Gallego-Zazo, et al.
Gastroenterology
|
October 1, 1996
Randomized trial comparing albumin, dextran 70, and polygeline in cirrhotic patients with ascites treated by paracentesis
A Ginès, G Fernández-Esparrach, A Monescillo, et al.
Clinical Genetics
|
August 27, 2024
Non-immune hydrops fetalis is associated with bi-allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene
Jair Tenorio-Castano, Elena Mansilla Aparicio, Fe Amalia García Santiago, et al.
Page
of 91
Search research articles
Search
Showing results (831-840 of 908) with videos related to
Sort By:
Page
of 91
Human Mutation
|
September 9, 2020
Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene
Francesca Piceci-Sparascio, Adrian Palencia-Campos, Patricia Soto-Bielicka, et al.
European Journal of Human Genetics : EJHG
|
September 30, 2025
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder
Asier Iturrate, Nurit Assia Batzir, Ranit Jaron, et al.
Frontiers in Oncology
|
March 9, 2026
Advances in intratumoral immunotherapy from a neuro-immune-endocrine perspective for breast cancer treatment
Claudia Angélica Garay-Canales, Mariana Segovia-Mendoza, Yair Rodríguez-Santiago, et al.
The Science of the Total Environment
|
January 25, 2016
Airborne pollen trends in the Iberian Peninsula
C Galán, P Alcázar, J Oteros, et al.
Journal of Medicinal Chemistry
|
March 4, 1998
Discovery of ritonavir, a potent inhibitor of HIV protease with high oral bioavailability and clinical efficacy
D J Kempf, H L Sham, K C Marsh, et al.
American Journal of Human Genetics
|
June 13, 1998
Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region
S Monk, A Sakuntabhai, S A Carter, et al.
Cell Reports
|
March 23, 2022
A 3D transcriptomics atlas of the mouse nose sheds light on the anatomical logic of smell
Mayra L Ruiz Tejada Segura, Eman Abou Moussa, Elisa Garabello, et al.
Frontiers in Medicine
|
December 12, 2025
Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in <i>FAM83G</i>
Mónica Mora-Gómez, Marta Feito, Natalia Gallego-Zazo, et al.
Gastroenterology
|
October 1, 1996
Randomized trial comparing albumin, dextran 70, and polygeline in cirrhotic patients with ascites treated by paracentesis
A Ginès, G Fernández-Esparrach, A Monescillo, et al.
Clinical Genetics
|
August 27, 2024
Non-immune hydrops fetalis is associated with bi-allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene
Jair Tenorio-Castano, Elena Mansilla Aparicio, Fe Amalia García Santiago, et al.
Page
of 91