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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Disease and CACNA1F[original query]
Genotyping microarray for CSNB-associated genes.
Investigative ophthalmology & visual science 2009 Dec 50 (12): 5919-26.
Zeitz Christina, Labs Stephan, Lorenz Birgit, Forster Ursula, Uksti Janne, Kroes Hester Y, De Baere Elfride, Leroy Bart P, Cremers Frans P M, Wittmer Mariana, van Genderen Maria M, Sahel José-Alain, Audo Isabelle, Poloschek Charlotte M, Mohand-Saïd Saddek, Fleischhauer Johannes C, Hüffmeier Ulrike, Moskova-Doumanova Veselina, Levin Alex V, Hamel Christian P, Leifert Dorothee, Munier Francis L, Schorderet Daniel F, Zrenner Eberhart, Friedburg Christoph, Wissinger Bernd, Kohl Susanne, Berger Wolfga
Ca1.4 calcium channels control cytokine production by human peripheral T17 cells and psoriatic skin-infiltrating T cells.
The Journal of allergy and clinical immunology 2021 10 149 (4): 1348-1357.
Mars Marion, Néant Isabelle, Leclerc Catherine, Bosch Stéphanie, Rouviere Christian, Moreau Marc, Lachambre Simon, Paul Carle, Tauber Marie, Gravier Eléonore, Douzal Clara, Duplan Hélène, Babin Marine, Brocario Alexia, Thouvenin Marie-Dominique, Guéry Jean-Charles, Redoules Daniel, Lestienne Fabrice, Pelletier Lucette, Savignac Maga
A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness.
Genes 2021 1 12 (2): .
Mahmood Usman, Méjécase Cécile, Ali Syed M A, Moosajee Mariya, Kozak Ig
Two novel CACNA1F gene mutations cause two different phenotypes: Aland Eye Disease and incomplete Congenital Stationary Night Blindness.
Experimental eye research 2022 6 221 109143.
Mihalich Alessandra, Cammarata Gabriella, Tremolada Gemma, Pollazzon Marzia, Di Blasio Anna Maria, Marzoli Stefania Bianc
Congenital Stationary Night Blindness: Clinical and Genetic Features.
International journal of molecular sciences 2022 12 23 (23): .
Kim Angela H, Liu Pei-Kang, Chang Yin-Hsi, Kang Eugene Yu-Chuan, Wang Hung-Hsuan, Chen Nelson, Tseng Yun-Ju, Seo Go Hun, Lee Hane, Liu Laura, Chao An-Ning, Chen Kuan-Jen, Hwang Yih-Shiou, Wu Wei-Chi, Lai Chi-Chun, Tsang Stephen H, Hsiao Meng-Chang, Wang Nan-K
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis.
International journal of molecular sciences 2022 10 23 (19): .
Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee
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