Corvidae in Pakistan are Represented by Two Distinct Clades Revealed through Maternally Inherited Gene Region
نویسندگان
چکیده
منابع مشابه
Maternally Inherited Type 2 Diabetes and Deafness: Clinical and Molecular Aspect in Pakistan
Background:. A3243G mutation in tRNA Leu (UUR) leads to a specific clinical syndrome characterized by diabetes and sensorineural hearing defect, hence called as “Maternally Inherited Diabetes and Deafness (MIDD)”.. Methods: The study was retrospective, analytical case control study. Non probability convenient sampling technique was used. Subjects were divided into two groups. Thirty-nine patien...
متن کاملShoulder Arthroplasty Utilization by Race - Are Black Patients Under-Represented?
INTRODUCTION The purpose of this study is to analyze national and institutional trends in shoulder arthroplasty utilization by race. METHODS The Nationwide Inpatient Sample (NIS) was analyzed to determine racial trends in shoulder arthroplasty utilization nationally. An institutional database was then utilized to retrospectively identify all patients undergoing shoulder arthr...
متن کاملTwo Host Clades, Two Bacterial Arsenals: Evolution through Gene Losses in Facultative Endosymbionts
Bacterial endosymbiosis is an important evolutionary process in insects, which can harbor both obligate and facultative symbionts. The evolution of these symbionts is driven by evolutionary convergence, and they exhibit among the tiniest genomes in prokaryotes. The large host spectrum of facultative symbionts and the high diversity of strategies they use to infect new hosts probably impact the ...
متن کاملMaternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients
Intellectual disability (ID) and autism spectrum disorders (ASDs) are complex neuropsychiatric conditions, with overlapping clinical boundaries in many patients. We identified a novel intragenic deletion of maternal origin in two siblings with mild ID and epilepsy in the CADPS2 gene, encoding for a synaptic protein involved in neurotrophin release and interaction with dopamine receptor type 2 (...
متن کاملCerebellopontine angle tumor in a patient with a maternally inherited SDHD gene mutation.
Acoustic neuromas are the most common tumor in the cerebellopontine angle (CPA) but are rare in the general population. Paragangliomas are rarer still and, in a minority of cases (20%), are known to be caused by errors in the SDHD gene. Mutations in this gene are highly penetrant when inherited paternally but not maternally. We present the first reported case of a patient with a CPA tumor and a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Pakistan Journal of Zoology
سال: 2023
ISSN: ['0030-9923']
DOI: https://doi.org/10.17582/journal.pjz/20211209111259