Three novel mutations in the COL4A5 gene in Mexican Alport syndrome patients

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Hong Kong medical journal = Xianggang yi xue za zhi·2026

[Cardiovascular disease before and after COVID-19 infection: One-year survival].

Semergen·2023

Dietary supplementation of cystinotic mice by lysine inhibits the megalin pathway and decreases kidney cystine content.

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Association of tyrosine hydroxylase 01 (TH01) microsatellite and insulin gene (INS) variable number of tandem repeat (VNTR) with type 2 diabetes and fasting insulin secretion in Mexican population.

Journal of endocrinological investigation·2023

The role of single nucleotide variant rs3819817 of the Histidine Ammonia-Lyase gene and 25-Hydroxyvitamin D on bone mineral density, adiposity markers, and skin pigmentation, in Mexican population.

Journal of endocrinological investigation·2023

Assessment of the Relationship Between Inflammation and Glomerular Filtration Rate.

Canadian journal of kidney health and disease·2023

Expanding Clinical and Variant Spectrum of CBX1-Related Syndrome: Report of Three Novel Cases.

Clinical genetics·2026

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

A Homozygous ALCAM-CBLB Deletion at 3q13.11-q13.12 Defines a Candidate Novel Oculo-Skeletal-Immune Contiguous Gene Deletion Syndrome.

Clinical genetics·2026

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

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Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

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A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Clinical genetics·2026

Identification of metabolites that influence flavor in the flesh of six mango cultivars from Thailand.

Food chemistry·2026

The Tapu-Noa Matrix for Determining Whether the Use or Registration of a Trade Mark Is Likely to Offend Māori.

Journal of the Royal Society of New Zealand·2026

Exploring the Mechanism of Umami Peptide Binding with the T1R1/T1R3 Receptor via Molecular Dynamics Simulations.

Molecules (Basel, Switzerland)·2026

Possible somatosensory modulation of tinnitus in a patient with temporomandibular joint disorder: An fMRI/TMJ-MRI case report (3-Month Follow-Up) Vasil Pehnyo1, Nataliia Savychuk1, Oleksandr Bida2, Stanislav Riebienkov3, Ivan Riabko4, Roman Sulik1 1SHUPYK NATIONAL HEALTHCARE UNIVERSITY OF UKRAINE, KYIV, UKRAINE 2BOGOMOLETS NATIONAL MEDICAL UNIVERSITY, KYIV, UKRAINE 3 NATIONAL CHILDREN'S SPECIALIZED HOSPITAL "OKHMATDYT", KYIV, UKRAINE 4TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV, KYIV, UKRAINE Wiad Lek. 2026;79(2): -. doi.

Wiadomosci lekarskie (Warsaw, Poland : 1960)·2026

An Update on the Epidemiology of Tusi ("Pink Cocaine").

Current addiction reports·2026

Pharmacokinetics of the potassium-competitive acid blocker tegoprazan administered by the oral route in healthy Mexicans.

International journal of clinical pharmacology and therapeutics·2026

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Three novel mutations in the COL4A5 gene in Mexican Alport syndrome patients

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Kidney health for all: caring for people, protecting the planet.

[Cardiovascular disease before and after COVID-19 infection: One-year survival].

Dietary supplementation of cystinotic mice by lysine inhibits the megalin pathway and decreases kidney cystine content.

Association of tyrosine hydroxylase 01 (TH01) microsatellite and insulin gene (INS) variable number of tandem repeat (VNTR) with type 2 diabetes and fasting insulin secretion in Mexican population.

The role of single nucleotide variant rs3819817 of the Histidine Ammonia-Lyase gene and 25-Hydroxyvitamin D on bone mineral density, adiposity markers, and skin pigmentation, in Mexican population.

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Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

A Homozygous ALCAM-CBLB Deletion at 3q13.11-q13.12 Defines a Candidate Novel Oculo-Skeletal-Immune Contiguous Gene Deletion Syndrome.

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Identification of metabolites that influence flavor in the flesh of six mango cultivars from Thailand.

The Tapu-Noa Matrix for Determining Whether the Use or Registration of a Trade Mark Is Likely to Offend Māori.

Exploring the Mechanism of Umami Peptide Binding with the T1R1/T1R3 Receptor via Molecular Dynamics Simulations.

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Three novel mutations in the COL4A5 gene in Mexican Alport syndrome patients

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