Results 81 to 90 of about 39,876 (186)

Harnessing Spatial and Multi‐Criteria Decision Analysis (MCDA) to Optimize Land Suitability for Kenaf Cultivation in Kelantan: Pathways for Sustainable Economic Development

Land Degradation &Development, Volume 37, Issue 15, Page 11438-11458, September 2026.
ABSTRACT In Kelantan, entrenched land degradation and extensive idling of agricultural lands exacerbate rural poverty. Current top‐down planning often overlooks local geographic and social constraints, despite state initiatives to convert idle lands and strengthen rural livelihoods.
Nur Afiqah Ariffin, Zainol Jamil, Yaniza Shaira Zakaria, Nur Ain Che Mat Ali, Azizul Ahmad   +4 more
wiley   +1 more source

Doa sepanjang masa.

, 2015
Buku ini menghimpun sejumlah doa sehari-hari dilengkapi dengan sumber dan terjemahan.iv, 100 hlm.: ilus.; 21 ...

core  

High Resolution Direction of Arrival (DOA) Estimation Based on Improved Orthogonal Matching Pursuit (OMP) Algorithm by Iterative Local Searching

Sensors, 2013
DOA (Direction of Arrival) estimation is a major problem in array signal processing applications. Recently, compressive sensing algorithms, including convex relaxation algorithms and greedy algorithms, have been recognized as a kind of novel DOA ...
Renbiao Wu, Wenyi Wang
doaj   +1 more source

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

Movement Disorders Clinical Practice, Volume 13, Issue 9, Page 2250-2258, September 2026.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan, Laura Tochen, Jacky Ganguly, Sayoni Roy Chowdhury, Haya S AlFaris, Vivek Pai, Andrea LeBlanc‐Millar, Sara Breitbart, Hrishikesh Kumar, Manohar Shroff, Arun Reginald, Grace Yoon, Alfonso Fasano, George M Ibrahim, Carolina Gorodetsky   +14 more
wiley   +1 more source

Doa Ajaran Allah dan Rasul : Doa anak untuk orang tua, Doa orang tua untuk anak

, 2011
Denagan selalu membaca doa anda diharapkan senantiasa mampu merangkuh kebaikan dan terhimdar dari keburukan165 hlm, : 16 x 16 ...
khalifurrahman
core  

Obstructive sleep apnea and major depressive disorder: Shared transcriptional signatures and candidate pathways identified via bioinformatics analysis

Sleep Research, Volume 3, Issue 3, Page 242-250, September 2026.
Abstract Background Obstructive sleep apnea (OSA) frequently co‐occurs with major depressive disorder (MDD). However, the underlying biological mechanisms remain unclear. This study aimed to identify OSA‐related transcriptional signatures associated with depressive status using integrated bioinformatics and machine learning.
Yun‐Shu Sun, Fei Wang, Qian‐Ting Zhong, Shi‐Bin Wang, Fu‐Jun Jia, Cai‐Lan Hou   +5 more
wiley   +1 more source

Dahsyatnya Doa-Doa di dalam Al-qur'an

, 2016
BUKU INI BERISI BERBAGAI MACAM DOA DI DALAM AL-QURAN YANG AMPUH KARENA MEMANG DARI FIRMAN ALLAH SENDIRI. MEMEMUAT DOA MUJARAB MEMOHON BERLIMPAH REJEKI, MEMOHON ANAK, MEMOHON ANAK LAKI-LAKI, MEMOHON ANAK TUMBUH SEHAT, MEMOHON KESHOLEHAN, DAN LALIN-LAIN ...
Maryam Kinanthi
core  

Doa iftitah : teks dan penjelasan

, 2015
Buku ini berisi tentang doa iftitah beserta teks dan penjelasannya.196 hlm.; 20 ...
Arif Mulyadi, Miqdad Turkan, Husain Nahrawi, Muhammad Husain Fadhlullah   +3 more
core   +1 more source

Doa-doa / Mariana Mohamed Sam [PDF]

, 2002
Sejajar dengan perkembangan pesat penggunaan elemen-elemen mutlimedia dalam kehidupan maka 1 pakej multimedia tentang DOA akan dibangunkan yang bertujuan memberi alternatif serta mewarnai pembelajaran secara tidak formal tentang amalan-amalan dalam Islam.
Mariana, Mohamed Sam
core   +1 more source

Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy

eLife
Autosomal dominant optic atrophy (DOA) is a progressive form of blindness caused by degeneration of retinal ganglion cells and their axons, mainly caused by mutations in the OPA1 mitochondrial dynamin like GTPase (OPA1) gene.
Yohei Nitta, Jiro Osaka, Ryuto Maki, Satoko Hakeda-Suzuki, Emiko Suzuki, Satoshi Ueki, Takashi Suzuki, Atsushi Sugie   +7 more
doaj   +1 more source