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  • 1-10 ل  10 نتائج ل ""Models, Molecular""
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Geographic : pakistan
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Academic Journal

Characterization of rifampicin-resistant Mycobacterium tuberculosis in Khyber Pakhtunkhwa, Pakistan.

  • Authors : Khan AS; Department of Microbiology, Kohat University of Science and Technology, Kohat, Pakistan.; Provincial Tuberculosis Reference, Laboratory Hayatabad Medical Complex, Peshawar, Pakistan.

Subjects: Antitubercular Agents/Antitubercular Agents/Antitubercular Agents/*pharmacology ; Mycobacterium tuberculosis/Mycobacterium tuberculosis/Mycobacterium tuberculosis/*genetics ; Rifampin/Rifampin/Rifampin/*pharmacology

  • Source: Scientific reports [Sci Rep] 2021 Jul 09; Vol. 11 (1), pp. 14194. Date of Electronic Publication: 2021 Jul 09.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Identification of Hearing Loss-Associated Variants of PTPRQ , MYO15A , and SERPINB6 in Pakistani Families.

  • Authors : Mahmood U; Department of Biochemistry, Government College University, Faisalabad 38000, Pakistan.; Bukhari SA

Subjects: Genetic Predisposition to Disease*; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Mutation/Mutation/Mutation/*genetics

  • Source: BioMed research international [Biomed Res Int] 2021 Apr 24; Vol. 2021, pp. 5584788. Date of Electronic Publication: 2021 Apr 24 (Print Publication: 2021).Publisher: Wiley Country of Publication: United States NLM ID: 101600173 Publication Model: eCollection Cited Medium: Internet ISSN: 2314-6141

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Academic Journal

Two homozygous missense mutations in ITGB3 gene as a cause of Glanzmann Thrombasthenia in four consanguineous Pakistani pedigrees.

  • Authors : Ali T; Department of Human Genetics and Molecular Biology, University of Health Sciences, Lahore, Pakistan.; Gul S

Subjects: Homozygote* ; Mutation, Missense*; Integrin beta3/Integrin beta3/Integrin beta3/*genetics

  • Source: International journal of laboratory hematology [Int J Lab Hematol] 2020 Oct; Vol. 42 (5), pp. 628-635. Date of Electronic Publication: 2020 Jun 19.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.

  • Authors : Borhany M; Department of Haematology, Haemostasis & Thrombosis, National Institute of Blood Disease and Bone Marrow Transplantation (NIBD), Karachi, Pakistan.; Handrkova H

Subjects: DNA Mutational Analysis* ; Mutation* ; Pedigree*

  • Source: Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2014 Jul; Vol. 20 (4), pp. 568-74. Date of Electronic Publication: 2013 Dec 16.Publisher: Blackwell Science Country of Publication: England NLM ID: 9442916 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.

  • Authors : Shafique S; COMSATS Institute of Information Technology, Park Road, Islamabad, Pakistan.; Siddiqi S

Subjects: Genomics* ; Pedigree*; Genes, Recessive/Genes, Recessive/Genes, Recessive/*genetics

  • Source: PloS one [PLoS One] 2014 Jun 20; Vol. 9 (6), pp. e100146. Date of Electronic Publication: 2014 Jun 20 (Print Publication: 2014).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Academic Journal

Leptin deficiency and leptin gene mutations in obese children from Pakistan.

  • Authors : Fatima W; Department of Human Genetics and Molecular Biology, University of Health Sciences, Lahore, Pakistan.; Shahid A

Subjects: Mutation*; Leptin/Leptin/Leptin/*deficiency ; Leptin/Leptin/Leptin/*genetics

  • Source: International journal of pediatric obesity : IJPO : an official journal of the International Association for the Study of Obesity [Int J Pediatr Obes] 2011 Oct; Vol. 6 (5-6), pp. 419-27. Publisher: Informa Healthcarep Country of Publication: England NLM ID: 101256330 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Development of agriculture biotechnology in Pakistan.

  • Authors : Zafar Y; Pakistan Atomic Energy Commission, Agriculture and Biotechnology Division, PO Box No. 1114, Islamabad, Pakistan.

Subjects: Biotechnology/Biotechnology/Biotechnology/*methods ; Crops, Agricultural/Crops, Agricultural/Crops, Agricultural/*genetics; Agriculture

  • Source: Journal of AOAC International [J AOAC Int] 2007 Sep-Oct; Vol. 90 (5), pp. 1500-7.Publisher: Oxford University Press Country of Publication: England NLM ID: 9215446 Publication Model: Print Cited Medium: Print ISSN: 1060-3271

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Academic Journal

Halosterols A and B, chymotrypsin inhibitory sterols from Haloxylon recurvum.

  • Authors : Hussain S; Department of Chemistry, Baghdad-ul-Jadid Campus, Islamia University, Bahawalpur, Pakistan.; Ahmed E

Subjects: Chenopodiaceae/Chenopodiaceae/Chenopodiaceae/*chemistry ; Cholesterol/Cholesterol/Cholesterol/*analogs & derivatives ; Chymotrypsin/Chymotrypsin/Chymotrypsin/*antagonists & inhibitors

  • Source: Chemical & pharmaceutical bulletin [Chem Pharm Bull (Tokyo)] 2006 May; Vol. 54 (5), pp. 623-5.Publisher: Pharmaceutical Society of Japan Country of Publication: Japan NLM ID: 0377775 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Identification of a new Leu354Pro mutation responsible for factor XIII deficiency.

  • Authors : Anwar R; Molecular Medicine Unit, University of Leeds, Clinical Sciences Building, St James's University Hospital, Leeds, UK. ; Gallivan L

Subjects: Point Mutation*; Factor XIII Deficiency/Factor XIII Deficiency/Factor XIII Deficiency/*genetics; Adult

  • Source: European journal of haematology [Eur J Haematol] 2001 Feb; Vol. 66 (2), pp. 133-6.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print Cited Medium: Print ISSN: 0902-4441 (Print)

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Academic Journal

Identification of a new mutation (Gly420Ser), distal to the active site, that leads to factor XIII deficiency.

Subjects: Mutation, Missense*; Factor XIII/Factor XIII/Factor XIII/*chemistry ; Factor XIII Deficiency/Factor XIII Deficiency/Factor XIII Deficiency/*genetics

  • Source: European journal of haematology [Eur J Haematol] 2000 Oct; Vol. 65 (4), pp. 279-84.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print Cited Medium: Print ISSN: 0902-4441 (Print)

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  • 1-10 ل  10 نتائج ل ""Models, Molecular""