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Bibliography

‘Ākif Sa‘īd, Ḥāfiẓ (Mudīr-e-A‘lā), Nidā-e-Khilāfat (weekly), Anjuman Khuddām al-Qur’ān, Lāhore.

‘Ākif Sa‘īd,Ḥāfiẓ (Mudīr-e-A‘lā), Mīthāq (monthly), Anjuman Khuddām al-Qur’ān ,Lāhore.

‘Abd al-‘Azīz, Shāh, Malfūẓāt (Persian), Maṭba‘ah Mujṭabāī’, Mīrath, 1314 A.H.

‘Abd al-Ḥayy, Nuzhat al-Khawāṭir, Ḥyderābād (Deccan), 1979 A.D.

‘Abd al-Qādir, Shāh, Mūḍiḥ-i-Qur’ān,Tāj Company Ltd, n.d.

‘Abd al-Ra’ūf Zafar, Dr., Maqālāt-e-Qur’ān Conference, The Islāmia University of Bahawalpūr, 2009A.D.

Ḥassān, Ḥusain Ḥamīd, Al-Daktūr,Ḥukm al-Sharī‘ah al-Islāmia fī ‘Aqūd al-tāmīn, Dār al-I‘taṣām, Cairo,1969 A.D.

Āzād, Abu’l- Kalām, Makātīb Abu’l-Kalām Āzād, Urdu Academy, Karāchī, n.d.

Āzād, Abu’l-Kalām, Tajumān al-Qur’ān, Saḥiyah Academy, New Delhi, 1968A. D.

Aḥmad Ḥasan, Syed, Aḥsan al-Tafāsīr, Maktabah al-salafiyah, Lāhore, 2008A.D.

Afrīqī, Ibn-e-Manẓūr, Lisān al-‘Arab, Dār Ihyā al-turāth al-‘Arabī Lil ṭab‘ati walnashr wal tauzī‘, Bairūt, 1408 A.H.

Al-Ẓiā (monthly), Lakhnow.

Al-Haethmī, Nūr al-Dīn ‘Alī bīn Abī Bakr, Ḥāfiẓ, Majma‘-al-Zawā‘id, Maṭbū‘ah Dār al-Kitāb al-‘Arabī, Bairūt, 1402 A.H.

Al-Kasānī, Abū Bakr, Badā’i al-Ṣanā’i‘, Cairo, 1990 A.D.

Al-Māwardī, Abu’l-Ḥasan ‘Alī bin Muḥammad Bin Ḥabīb, Al-aḥkām al-Sulṭāniyah, Dār al-Kitāb al-‘Arabī, Bairūt, 1420 A.H.

Anwar Shāh, Kashmīrī, Anwār al-Bārī,Idārah Tālīf-e-Ashrafīyah, Multān, n.d.

Athar Mubārakpūrī, Qāḍī, Hindustān Main ‘Arbōn KīḤakūmatain, Maktabah ‘Ārfīn, Karāchī,1965A.D.

Balouch, Nabī Bakhsh Khān, Dr., Sindhī Bolī Adab Jī Tārīkh, Pākistān Study Centre, Sindh University,Jām Shoro,1990A.D.

Bhattī, Muḥammad Isḥāque, Barraesaghīr Pāk-o-Hind Mein ‘Ilm-e-Fiqh, Idārah Thaqāfat-e-Islāmiah, Lāhore,1973A.D.

Bukhārī, Muḥammad bin Ismā‘īl, Ṣaḥīḥ al-Bukhārī, Dār al-Salām, Al-Riāẓ, 1419 A. H.

Bukhāri, Syed Maḥmūd Shāh, Dr.,Waṭan ji Āzādi jo Imām, Shahbāz Publication, Ḥyderābād, Sindh,1984 A.D.

Burhān al-dīn, ‘Alī bin abī Bakr, Al-hidāyah Sharaḥ Al-bidāyah, Dār al- kutab al-‘Ilmiyah, Bairūt, 1990 A.D.

Encyclopedia Britanica, London, 1958.

دعوت کے میدان میں تبلیغی جماعت کے مساعی و مشکلات کا تحقیقی جائزہ

Muhammad (PBUH) was the last Prophet. Almighty Allah sent Him message to preach the people, but the Kufar made His enemies. Instead the situation of opposition and hatred from his enemies how He treated them with patience and love. And how He would be able to establish Islamic states and invites the people of other areas towards Islam. Muhammad (PBUH) was succeeded from the reformers of his ummah and among these reformers were the founder of tableghi jammat, Molana Muhammad Ilyas Kandhalwi. This research paper will compare the difficulties of Muhammad's (PBUH) Da'wah with tableghi Jammat.                       

Mutationalscreening of Thalassemia Affected Families in Rahim Yar Khan

Thalassemia is an autosomal recessive blood disorder, and this is the second most abundant genetic disorder, of which 50% of patients are from the Southeast Asian region. Beta-Haemoglobin (HBB) gene carries the mutation, and the alteration in the HBB gene sequence results in the abnormal functioning of oxygen-carrying hemoglobin molecules. This study was conducted on the 20 affected families of Thalassemia after their consent. Blood samples were collected. Then DNA was extracted using a standard organic method with some modifications. Primers for the exonic and intronic region of the HBB gene were designed and amplified following PCR protocol. Amplicons were sequenced for mutation detection using bioinformatic tools. The previous researches show that incorrect intronic and exonic splicing lead the thalassemia to reach at worst condition due to defect in mutation. The Human Splicing Finder (HSF) tool, BLAST tool from NCBI website, and Bioedit software have been used for analyzing the sequence and variations at positions. Five different samples of the HBB gene showed differences in different locations of exon and intron. HBB Exon 1 Sample 1 has intronic change with variation in base change position c269+5 on an amplified fragment from G>C. HBB Exon 1 Sample 2 has exonic change with variation in base change position c185 on an amplified fragment from T>C of nucleotide change, and codon replacement occurs at position CAT>CAC as amino acid p.His does not change. HBB Exon 1 Sample 3 has intronic change with variation in base change position c269+5 on an amplified fragment from G>C. HBB Exon 1 Sample 4 has exonic change with variation in base change position c185 on an amplified fragment from T>C of nucleotide change, and codon replacement occurs at position CAT>CAC as amino acid p.His does not change. HBB Exon 2 Sample 5 has intronic change with variation in base change position c491+16 on an amplified fragment from G>C. Graphical Representation and chromatogram of Potential splice site are showing intronic and exonic variations at the position. G replaces C in samples of intronic variation & T replaces C in samples of exonic variation. Change in sequence alignment is observed at different positions in samples of exons and introns. This study concludes that the change in the HBB gene is observed as well as intronic, and exonic splicing can lead thalassemia from severe to mild.
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