Cargando…

Sequencing MODY1-6 genes in Uyghur Early-onset diabetes pedigree

Detalles Bibliográficos
Autores principales:	Nuli, Rebiya, Mohemaiti, Patamu, Yimamu, Yilihamujan, Taxitiemuer, Aierken
Formato:	Texto
Lenguaje:	English
Publicado:	Medknow Publications 2011
Materias:	Letters to Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079876/ https://www.ncbi.nlm.nih.gov/pubmed/21584173 http://dx.doi.org/10.4103/2230-8210.77591

Ejemplares similares

Metagenomics and Faecal Metabolomics Integrative Analysis towards the Impaired Glucose Regulation and Type 2 Diabetes in Uyghur-Related Omics
por: Nuli, Rebiya, et al.
Publicado: (2019)

Integrative Analysis Toward Different Glucose Tolerance-Related Gut Microbiota and Diet
por: Nuli, Rebiya, et al.
Publicado: (2019)

Interaction between dietary patterns and TCF7L2 polymorphisms on type 2 diabetes mellitus among Uyghur adults in Xinjiang Province, China
por: Cai, Junxiu, et al.
Publicado: (2019)

Letter to the Editor: Stress Hyperglycemia or Glucokinase Maturity Onset Diabetes of the Young (GCK-MODY) or Both?
por: Doherty-Kirby, Amanda
Publicado: (2023)

CDK6 3'UTR polymorphisms alter the susceptibility to cervical cancer among Uyghur females
por: Aierken, Kailibinuer, et al.
Publicado: (2019)

Clinical and genetic features of Epstein‐Barr virus‐triggered late‐onset primary hemophagocytic lymphohistiocytosis: Ten pedigrees study
por: Gao, Lili, et al.
Publicado: (2021)

A predictive model for hyperuricemia among type 2 diabetes mellitus patients in Urumqi, China
por: Abudureyimu, Palizhati, et al.
Publicado: (2023)

Single patient in GCK-MODY family successfully re-diagnosed into GCK-PNDM through targeted next-generation sequencing technology
por: Antosik, Karolina, et al.
Publicado: (2015)

A missense TCF1 mutation in a patient with mody‐3 and liver adenomatosis
por: Lerario, Antonio Marcondes, et al.
Publicado: (2010)

Functional Characterization of a Novel Heterozygous Mutation in the Glucokinase Gene That Causes MODY2 in Chinese Pedigrees
por: Jiang, Feng, et al.
Publicado: (2021)

Clinical features and treatment of maturity onset diabetes of the young (MODY)
por: Gardner, Daphne SL, et al.
Publicado: (2012)

Update on clinical screening of maturity-onset diabetes of the young (MODY)
por: Peixoto-Barbosa, Renata, et al.
Publicado: (2020)

Response to: DNA identification by pedigree likelihood ratio accommodating population substructure and mutations
por: Egeland, Thore, et al.
Publicado: (2011)

Early Onset of Liver Steatosis in a Japanese Girl with Maturity-Onset Diabetes of the Young Type 3 (MODY3)
por: Nakamura, Akie, et al.
Publicado: (2012)

MN1 gene loss-of-function mutation causes cleft palate in a pedigree
por: Shu, Li, et al.
Publicado: (2020)

Maturity-onset diabetes of the young (MODY): current perspectives on diagnosis and treatment
por: Urakami, Tatsuhiko
Publicado: (2019)

At what age should the Uyghur minority initiate cervical cancer screening if screened using careHPV
por: Abulizi, Guzhalinuer, et al.
Publicado: (2021)

Response to: DNA identification by pedigree likelihood ratio accommodating population substructure and mutations- authors' reply
por: Chakraborty, Ranajit, et al.
Publicado: (2011)

Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples
por: Mulder, René, et al.
Publicado: (2020)

Precision diabetes: Lessons learned from maturity‐onset diabetes of the young (MODY)
por: Tosur, Mustafa, et al.
Publicado: (2022)

Challenges for Molecular Diagnosis of Familial Early-Onset Diabetes in Unexplored Populations
por: AMARA, Abdelbasset, et al.
Publicado: (2014)

Neuroplasticity in Early Onset Multiple Sclerosis
por: Naser Moghadasi, Abdorreza
Publicado: (2014)

Exome Sequencing and Genetic Testing for MODY
por: Johansson, Stefan, et al.
Publicado: (2012)

Middle of the breasts pigmentation in a pedigree with POFUT1-related Dowling-Degos disease, expansion of the phenotype
por: Wu, Yingda, et al.
Publicado: (2021)

Granulicatella adiacens and Early-Onset Sepsis in Neonate
por: Bizzarro, Matthew J., et al.
Publicado: (2011)

Phenotype Heterogeneity in Glucokinase–Maturity-Onset Diabetes of the Young (GCK-MODY) Patients
por: Wędrychowicz, Anna, et al.
Publicado: (2017)

The epidemiology, molecular pathogenesis, diagnosis, and treatment of maturity-onset diabetes of the young (MODY)
por: Nkonge, Ken Munene, et al.
Publicado: (2020)

Late Diagnosis of Maturity-Onset Diabetes of the Young (MODY) 12 With Catastrophic Consequences
por: Carreira, Nuno R, et al.
Publicado: (2021)

Causal variants in Maturity Onset Diabetes of the Young (MODY) – A systematic review
por: Rafique, Ibrar, et al.
Publicado: (2021)

The coexistence of autoimmune diabetes and maturity-onset diabetes of the young (MODY): a case series
por: O’Donovan, Eimear Mary, et al.
Publicado: (2022)

Early onset of breast cancer in British black women
por: Cichowska, A, et al.
Publicado: (2008)

Is Alacrima So Prevalent in Patients With Early-Onset Achalasia?
por: Kim, Hee Man
Publicado: (2011)

Early and late-onset Alzheimer's disease: What are the differences?
por: Awada, Adnan A.
Publicado: (2015)

Coexistence of Amyotrophic Lateral Sclerosis in the Proband of an X-Linked Charcot-Marie-Tooth Disease Type 1 Pedigree in China
por: Feng, Shu-Yan, et al.
Publicado: (2018)

Associations of Residential Greenness with Diabetes Mellitus in Chinese Uyghur Adults
por: Fan, Shujun, et al.
Publicado: (2019)

Genomic diversity and post-admixture adaptation in the Uyghurs
por: Pan, Yuwen, et al.
Publicado: (2021)

Genetics and Pathophysiology of Maturity-onset Diabetes of the Young (MODY): A Review of Current Trends
por: Yahaya, Tajudeen O., et al.
Publicado: (2020)

Frequency and genetic spectrum of maturity-onset diabetes of the young (MODY) in southern New Zealand
por: Wheeler, Benjamin J, et al.
Publicado: (2013)

Precision therapy for three Chinese families with maturity-onset diabetes of the young (MODY12)
por: Li, Juyi, et al.
Publicado: (2022)

GCK gene mutations are a common cause of childhood‐onset MODY (maturity‐onset diabetes of the young) in Turkey
por: Haliloglu, Belma, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_m5t5vun5fdvem519brlalgha6k