Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Birgit, Budde"'
Publikováno v:
Plant Ecology and Evolution, Vol 155, Iss 3, Pp 363-378 (2022)
Background and aims – Chilgoza pine (Pinus gerardiana) is a near-threatened tree species from the north-western Himalayas. This species is the economically most important pine in Afghanistan because of its edible nuts; however, its distribution ran
Externí odkaz:
https://doaj.org/article/d37372ad44a642ac8529d11ab1a97076
Publikováno v:
Plant Ecology and Evolution 155(3): 363-378
Background and aims – Chilgoza pine (Pinus gerardiana) is a near-threatened tree species from the north-western Himalayas. This species is the economically most important pine in Afghanistan because of its edible nuts; however, its distribution ran
Autor:
Sajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, Ilyas Ahmad, Maria Iqbal, Syeda Seema Waseem, Maria Asif, Uzma Abdullah, Ehtisham Ul Haq Makhdoom, Emrah Kaygusuz, Muhammad Zakaria, Shafaq Ramzan, Saif ul Haque, Asif Mir, Iram Anjum, Mehak Fiaz, Zafar Ali, Muhammad Tariq, Neelam Saba, Wajid Hussain, Birgit Budde, Saba Irshad, Angelika Anna Noegel, Stefan Höning, Shahid Mahmood Baig, Peter Nürnberg, Muhammad Sajid Hussain
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Abstract Background Primary microcephaly (MCPH) is a congenital neurodevelopmental disorder manifesting as small brain and intellectual disability. It underlies isolated reduction of the cerebral cortex that is reminiscent of early hominids which mak
Externí odkaz:
https://doaj.org/article/86efdf4d011a4c569530b984fe472c83
Autor:
Syeda Seema Waseem, Abubakar Moawia, Birgit Budde, Muhammad Tariq, Ayaz Khan, Zafar Ali, Sheraz Khan, Maria Iqbal, Naveed Altaf Malik, Saif ul Haque, Janine Altmüller, Holger Thiele, Muhammad Sajid Hussain, Sebahattin Cirak, Shahid Mahmood Baig, Peter Nürnberg
Publikováno v:
Genes, Vol 12, Iss 10, p 1494 (2021)
Primary microcephaly (MCPH) is a prenatal condition of small brain size with a varying degree of intellectual disability. It is a heterogeneous genetic disorder with 28 associated genes reported so far. Most of these genes encode centrosomal proteins
Externí odkaz:
https://doaj.org/article/180af34144004e85ac38ff0161006275
Autor:
Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, Uzma Abdullah, Ghulam Hussain, Maria Asif, Birgit Budde, Wolfgang Höhne, Sigrid Tinschert, Saadia Maryam Saadi, Hammad Yousaf, Zafar Ali, Ambrin Fatima, Emrah Kaygusuz, Ayaz Khan, Muhammad Jameel, Sheraz Khan, Muhammad Tariq, Iram Anjum, Janine Altmüller, Holger Thiele, Stefan Höning, Shahid Mahmood Baig, Peter Nürnberg, Muhammad Sajid Hussain
Publikováno v:
Genes, Vol 12, Iss 5, p 731 (2021)
Congenital microcephaly is the clinical presentation of significantly reduced head circumference at birth. It manifests as both non-syndromic—microcephaly primary hereditary (MCPH)—and syndromic forms and shows considerable inter- and intrafamili
Externí odkaz:
https://doaj.org/article/49838f1ee16e4a27aa482cd632fc8f90
Autor:
Felix Gugerli, Benjamin Dauphin, Pascal Milesi, Santiago C Gonzalez-Martinez, Katharina Birgit Budde, Stephen Cavers
Past environmental changes have shaped the demographic history and genetic diversity of natural populations, yet the timescale and strength of these effects have not been investigated systematically and simultaneously for multiple phylogenetically di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb70417490090b33e1df5a6043840872
https://doi.org/10.1101/2023.01.05.522822
https://doi.org/10.1101/2023.01.05.522822
Publikováno v:
Silvae Genetica. 71:65-71
Common ash (Fraxinus excelsior L.) is an economically and ecologically important tree species in Europe acutely threatened by ash dieback. Here, we present a new set of Simple Sequence Repeat markers for F. excelsior and six related ash species based
Autor:
Katharina Birgit Budde, Sophie Hötzel, Markus Müller, Natia Samsonidze, Aristotelis C. Papageorgiou, Oliver Gailing
Tree species are suffering from changing and stressful environmental conditions worldwide.Fagus sylvaticaL., one of the most common Central European deciduous tree species showed symptoms of crown damage, a reduction in growth and increased mortality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b6796004d8f59b9932e0a2c5828c4bd
https://doi.org/10.1101/2022.12.06.519312
https://doi.org/10.1101/2022.12.06.519312
Autor:
Ilyas Ahmad, Ayaz Khan, Hafiza Noor Ul Ayan, Birgit Budde, Janine Altmüller, Asad Aslam Korejo, Gudrun Nürnberg, Holger Thiele, Muhmmad Tariq, Peter Nürnberg, Jeanette Erdmann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80ad5e9eb889c8eeca20f1fdf12c2d2e
http://edoc.mdc-berlin.de/22169/1/22169oa.pdf
http://edoc.mdc-berlin.de/22169/1/22169oa.pdf
Autor:
Muhammad Jawad Hassan, Holger Thiele, Mohammad R. Toliat, Haseeb Anwar, Birgit Budde, Ilknur Sur-Erdem, M. Asif, Ludwig Eichinger, Arwa Ishaq A. Khayyat, Maria Iqbal, Peter Nürnberg, Muhammad Tariq, Angelika A. Noegel, Jamshaid Mahmood Baig, Ehtisham Ul Haq Makhdoom, Ilyas Ahmed, Muhammad Sher, Sarah Fischer, Uzma Abdullah, Christian Becker, Sigrid Tinschert, Stefan Höning, Muhammad Mohsin Ali Khan, Naveed Altaf Malik, Muhammad Jameel, Muhammad Sajid Hussain, Emrah Kaygusuz, Shahid Mahmood Baig
Publikováno v:
Clinical Genetics. 100:486-488
Jawad syndrome is a multiple congenital anomaly and intellectual disability syndrome with mutation in RBBP8 reported only in two families. Here, we report on two new families from Pakistan and identified a previously reported variant in RBBP8, NM_002