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Results for
""Gene Frequency""[mesh_terms]

943 Results

Searching titles within these results

Thalassemia mutations and their clinical aspects in Japan.

Yukio Hattori

International journal of hematology 2003;76 Suppl 2():90-2

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Abstract

Mitochondrial diabetes mellitus.

H H J P Lemkes, G M C Janssen, J A Maassen

Journal of endocrinological investigation 2002;25(5):477-84

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Abstract

Genetics of otosclerosis.

Melissa Thys, Guy Van Camp

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2010;30(8):1021-32

Full Text

Abstract

Clinical and genetic characterization of a large cohort of patients with Wilson's disease in China.

Wenming Yang, Jing Zhang, Yue Yang, Ting Dong, Pei Pei, Xiang Li, Shijie Zhang

Translational neurodegeneration 2022;11(1):13

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Abstract

Angiotensin-converting enzyme gene polymorphism is correlated to diabetic retinopathy: a meta-analysis.

Viroj Wiwanitkit

Journal of diabetes and its complications 2008;22(2):144-6

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High carrier frequency for abetalipoproteinemia and evidence of a founder variant in a French-Canadian population.

Véronique Desgagné, Valérie Poulin, Géraldine Gosse, Lysanne Girard, Luigi Bouchard, Alexis Baass, Martine Paquette, Simon-Pierre Guay

Journal of clinical lipidology 2024;18(4):e625-e630

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Abstract

Hereditary/familial versus sporadic prostate cancer: few indisputable genetic differences and many similar clinicopathological features.

C Alberti

European review for medical and pharmacological sciences 2010;14(1):31-41

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Abstract

The role of neurotrophin genes involved in the vulnerability to gambling disorder.

Roser Granero, Mikel Etxandi, Isabel Baenas, Neus Solé-Morata, Sonia V Forcales, Susana Jiménez-Murcia, Fernando Fernández-Aranda, Philip Gorwood, Nicolás Ramoz, José M Menchón, Mónica Gómez-Peña, Carme Barrot, Manel Gené

Scientific reports 2022;12(1):6925

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Abstract

Increased Prevalence of Rare Sucrase-isomaltase Pathogenic Variants in Irritable Bowel Syndrome Patients.

Koldo Garcia-Etxebarria, Tenghao Zheng, Ferdinando Bonfiglio, Luis Bujanda, Aldona Dlugosz, Greger Lindberg, Peter T Schmidt, Pontus Karling, Bodil Ohlsson, Magnus Simren, Susanna Walter, Gerardo Nardone, Rosario Cuomo, Paolo Usai-Satta, Francesca Galeazzi, Matteo Neri, Piero Portincasa, Massimo Bellini, Giovanni Barbara, Daisy Jonkers, Shanti Eswaran, William D Chey, Purna Kashyap, Lin Chang, Emeran A Mayer, Mira M Wouters, Guy Boeckxstaens, Michael Camilleri, Andre Franke, Mauro D'Amato

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2019;16(10):1673-1676

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How does evolution work in superabundant microbes?

Mark Kirkpatrick, Dmitry A Filatov

Trends in microbiology 2024;32(9):836-846

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Abstract

An efficient and reliable DNA extraction method for preimplantation genetic diagnosis: a comparison of allele drop out and amplification rates using different single cell lysis methods.

Sung Ah Kim, Jung Ah Yoon, Moon Joo Kang, Young Min Choi, Soo Jin Chae, Shin Yong Moon

Fertility and sterility 2009;92(2):814-8

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Abstract

Variability and genetic structure of plant virus populations.

J M Malpica, A Fraile, F García-Arenal

Annual review of phytopathology 2002;39():157-86

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Abstract

PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations.

Yuval Itan, Bertrand Boisson, Laurent Abel, Jean-Laurent Casanova, Shen-Ying Zhang, Franck Rapaport, Benedetta Bigio, Peng Zhang

Bioinformatics (Oxford, England) 2019;34(24):4307-4309

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Abstract

Identification of Molecular Mechanisms Responsible for the MMP-9-1562C/T Dependent Differential Regulation of Matrix Metalloproteinase-9 Expression in Human Neuron-like Cells.

Klaudia Nowicka, Marcin Rylski, Aneta Brągiel-Pieczonka, Magdalena Ambrożek-Latecka, Sylwia Pabian-Jewuła

Genes 2023;14(11):2028

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Abstract

The Autosomal Short Tandem Repeat Polymorphisms Are Potentially Associated with Cardiovascular Disease Predisposition in the Latin American Population: A Mini Review.

Santiago Cadena-Ullauri, Aníbal Gaviria, Adriana Alexandra Ibarra-Rodríguez, Nieves Doménech, Viviana A Ruiz-Pozo, Rafael Tamayo-Trujillo, Elius Paz-Cruz, Patricia Guevara-Ramírez, Ana Karina Zambrano

BioMed research international 2023;2023():6152905

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Abstract

Results: 1 – 15 / 943

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Results for ""Gene Frequency""[mesh_terms]

Thalassemia mutations and their clinical aspects in Japan.

Mitochondrial diabetes mellitus.

Genetics of otosclerosis.

Clinical and genetic characterization of a large cohort of patients with Wilson's disease in China.

Angiotensin-converting enzyme gene polymorphism is correlated to diabetic retinopathy: a meta-analysis.

High carrier frequency for abetalipoproteinemia and evidence of a founder variant in a French-Canadian population.

Hereditary/familial versus sporadic prostate cancer: few indisputable genetic differences and many similar clinicopathological features.

The role of neurotrophin genes involved in the vulnerability to gambling disorder.

Increased Prevalence of Rare Sucrase-isomaltase Pathogenic Variants in Irritable Bowel Syndrome Patients.

How does evolution work in superabundant microbes?

An efficient and reliable DNA extraction method for preimplantation genetic diagnosis: a comparison of allele drop out and amplification rates using different single cell lysis methods.

Variability and genetic structure of plant virus populations.

PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations.

Identification of Molecular Mechanisms Responsible for the MMP-9-1562C/T Dependent Differential Regulation of Matrix Metalloproteinase-9 Expression in Human Neuron-like Cells.

The Autosomal Short Tandem Repeat Polymorphisms Are Potentially Associated with Cardiovascular Disease Predisposition in the Latin American Population: A Mini Review.

Results for
""Gene Frequency""[mesh_terms]