Publications by authors named "Muhammad Aminuddin"

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U-Pb zircon geochronology and geochemistry of Luk Ulo River boulders belong to Late Cretaceous-Paleocene metapsammite and metagranite of Luk Ulo Karangsambung, Central Java, Indonesia.
Muhammad Irman Khalif Ahmad Aminuddin, Mohd Shuaib, Naseem Akhtar, Nugroho Imam Setiawan, I Wayan Warmada

Environ Sci Pollut Res Int· May 2025

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Trigona honey effect on wound pH and healing in diabetes-related foot ulcers: A case series.
Sukarni Sukarni, Muhammad Aminuddin, Mao Kunimitsu, Kanae Mukai, Mayumi Okuwa

Complement Ther Clin Pract· May 2025

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Effectiveness of online education on thermography-based diabetic foot ulcer prevention for wound care specialists: a single-group quasi-experimental study.
Muhammad Aminuddin, Sukarni, Haryanto, Suriadi Jais, Amika Yamada

Diabetol Int· April 2025

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supplementation reduces MDA, TNF-α, and IL-6 levels in a rat model exposed to soot particulates.
Muhammad Aminuddin, Djanggan Sargowo, Teguh Wahju Sardjono, Widjiati Widjiati

Open Vet J· January 2023

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Metal chloride anion based ionic liquids: synthesis, characterization and evaluation of performance in hydrogen sulfide oxidative absorption.
Muhammad Syahir Aminuddin, Mohamad Azmi Bustam Khalil, Bawadi Abdullah

RSC Adv· April 2022

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Designing siRNA/chitosan-methacrylate complex nanolipogel for prolonged gene silencing effects.
Ye Cao, Yang Fei Tan, Yee Shan Wong, Muhammad Aminuddin, Bhuthalingam Ramya

Sci Rep· March 2022

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Mikania Micrantha Improved Memory Perform on Dementia Model.
Yuni Andriani, Siti Hamidatulaliyah, Desi Sagita, Muhammad Aminuddin

Open Access Maced J Med Sci· November 2019

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Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability.
Kirti Mittal, Muhammad A Rafiq, Rafiullah Rafiullah, Ricardo Harripaul, Hazrat Ali

J Hum Genet· October 2016

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Mutation of ATF6 causes autosomal recessive achromatopsia.
Muhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, Fareeha Zulfiqar, Kwanghyuk Lee

Hum Genet· September 2015

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Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.
Muhammad Arshad Rafiq, Claire S Leblond, Muhammad Arif Nadeem Saqib, Akshita K Vincent, Amirthagowri Ambalavanan

BMC Med Genet· June 2015

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Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.
Regie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, Muhammad Ansar, Muhammad Amin-Ud-Din

Hum Mol Genet· June 2014

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A nonsense mutation in the gene ROR2 underlying autosomal dominant brachydactyly type B.
Rabia Habib, Muhammad Amin-Ud-Din, Wasim Ahmad

Clin Dysmorphol· April 2013

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Fluorescent labeling of human albumin using the new aromatic dialdehyde labels and the study of innerfilter effect.
Muhammad Aminuddin, Sofia Ahmed, Muhammd Ali Sheraz, Iqbal Ahmad, Karamat Mahmood

J Pharm Bioallied Sci· October 2010

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Effect of caffeine complexation on the photolysis of riboflavin in aqueous solution: a kinetic study.
Iqbal Ahmad, Sofia Ahmed, Muhammad Ali Sheraz, Muhammad Aminuddin, Faiyaz Hussain Madni Vaid

Chem Pharm Bull (Tokyo)· December 2009

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Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
Zahid Azeem, Musharraf Jelani, Gul Naz, Muhammad Tariq, Naveed Wasif

Hum Genet· June 2008

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Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.
Peter John, Muhammad Tariq, Muhammad Arshad Rafiq, Muhammad Amin-Ud-Din, Dost Muhammad

Arch Dermatol Res· August 2006

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Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31.
Sajid Malik, Jörg Schott, Syed Wajahat Ali, Frank Oeffner, Muhammad Amin-ud-Din

Eur J Hum Genet· December 2005

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Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene.
Peter John, Muhammad Aslam, Muhammad Arshad Rafiq, Muhammad Amin-ud-din, Sayedul Haque

Arch Dermatol Res· November 2005

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A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin.
Sajid Malik, Muhammad Arshad, Muhammad Amin-Ud-Din, Frank Oeffner, Astrid Dempfle

Am J Med Genet A· April 2004

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