受强制性开放获取政策约束的文章 - Prof. Dr. Muhammad Wajid了解详情
无法在其他位置公开访问的文章：1 篇
Identification of mutations in the EDA and EDAR genes in Pakistani families with hypohidrotic ectodermal dysplasia
Y Shimomura, M Wajid, J Weiser, L Kraemer, Y Ishii, V Lombillo, SJ Bale, ...
Clinical genetics 75 (6), 582-584, 2009
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：31 篇
APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
Y Shimomura, D Agalliu, A Vonica, V Luria, M Wajid, A Baumer, S Belli, ...
Nature 464 (7291), 1043-1047, 2010
强制性开放获取政策： US National Institutes of Health
FGF5 is a crucial regulator of hair length in humans
CA Higgins, L Petukhova, S Harel, YY Ho, E Drill, L Shapiro, M Wajid, ...
Proceedings of the National Academy of Sciences 111 (29), 10648-10653, 2014
强制性开放获取政策： US National Institutes of Health
Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture
Y Shimomura, M Wajid, L Petukhova, M Kurban, AM Christiano
The American Journal of Human Genetics 86 (4), 632-638, 2010
强制性开放获取政策： US National Institutes of Health
Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis
Y Shimomura, M Wajid, L Petukhova, L Shapiro, AM Christiano
Journal of Investigative Dermatology 129 (3), 622-628, 2009
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Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas‐type polysyndactyly and Laurin‐Sandrow syndrome
S Lohan, M Spielmann, SC Doelken, R Flöttmann, F Muhammad, ...
Clinical Genetics 86 (4), 318-325, 2014
强制性开放获取政策： German Research Foundation
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome
RM Cabral, M Kurban, M Wajid, Y Shimomura, L Petukhova, ...
Genomics 99 (4), 202-208, 2012
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Hereditary leukonychia, or porcelain nails, resulting from mutations in PLCD1
M Kiuru, M Kurban, M Itoh, L Petukhova, Y Shimomura, M Wajid, ...
The American Journal of Human Genetics 88 (6), 839-844, 2011
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Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia
Y Ishii, M Wajid, H Bazzi, KA Fantauzzo, AG Barber, DC Blaydon, JS Nam, ...
Journal of Investigative Dermatology 128 (4), 867-870, 2008
强制性开放获取政策： US National Institutes of Health
Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis
Y Shimomura, M Wajid, A Zlotogorski, YJ Lee, RH Rice, AM Christiano
Journal of investigative dermatology 129 (8), 1927-1934, 2009
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NIPAL4/ichthyin is expressed in the granular layer of human epidermis and mutated in two Pakistani families with autosomal recessive ichthyosis
M Wajid, M Kurban, Y Shimomura, AM Christiano
Dermatology 220 (1), 8-14, 2010
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The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis
L Petukhova, Y Shimomura, M Wajid, P Gorroochurn, SE Hodge, ...
Human heredity 68 (2), 117-130, 2009
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A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance
M Kurban, M Wajid, L Petukhova, Y Shimomura, AM Christiano
Journal of human genetics 56 (10), 701-706, 2011
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A nonsense mutation in the SCN9A gene in congenital insensitivity to pain
M Kurban, M Wajid, Y Shimomura, AM Christiano
Dermatology 221 (2), 179-183, 2010
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Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma
MB Dua-Awereh, Y Shimomura, L Kraemer, M Wajid, AM Christiano
Journal of dermatological science 53 (3), 192-197, 2009
强制性开放获取政策： US National Institutes of Health
Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families
M Wajid, M Kurban, Y Shimomura, AM Christiano
Journal of dermatological science 56 (1), 27-32, 2009
强制性开放获取政策： US National Institutes of Health
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences
S Malik, KM Girisha, M Wajid, AK Roy, SR Phadke, S Haque, W Ahmad, ...
BMC Medical Genetics 8, 1-8, 2007
强制性开放获取政策： German Research Foundation
Splice site mutations in the P-cadherin gene underlie hypotrichosis with juvenile macular dystrophy
Y Shimomura, M Wajid, M Kurban, AM Christiano
Dermatology 220 (3), 208-212, 2010
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Evidence for a founder mutation in the cathepsin C gene in three families with Papillon-Lefèvre syndrome
M Kurban, M Wajid, Y Shimomura, R Bahhady, AG Kibbi, AM Christiano
Dermatology 219 (4), 289-294, 2009
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Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis
M Kurban, M Wajid, Y Shimomura, AM Christiano
Journal of the European Academy of Dermatology and Venereology 27 (5), 545-549, 2013
强制性开放获取政策： US National Institutes of Health
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